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Panel Update 5 PDF
Panel Update 5 PDF
Guide Legend
Panel Update 5
International
9020-7493 Rev. B
SMN 10714735
MicroScan , MICroSTREP plus , Synergies plus and WalkAway systems are trademarks of Siemens Healthcare
Diagnostics.
9020-7493, Rev. B
May 2013
9020-7493B
Page 2 of 158
Table of Contents
Revision Record ........................................................................................................................................................ 5
General Notes for Reporting Results: ..................................................................................................................... 6
DEFINITIONS: ............................................................................................................................................................. 6
INTERPRETIVE GUIDELINES ......................................................................................................................................... 6
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9020-7493B
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Rev.
Date
Affected Sections
March
2013
May
2013
Initial revision.
9020-7493B
Revision Record
Add NC54 panel to Note 2 of Fosfomycin Table with 16, 32 and 64 dilutions in the Dried Overnight and
Rapid (Fluorogenic) Gram-Negative Panels section
Page 5 of 158
The Interpretive Guidelines were based on the following references, unless otherwise noted.
Reference
EUCAST Clinical Breakpoint Tables
Revision
2013-02-11 (Version 3.1)
2013-01-01 (Version 3.0)
2012-01-01 (Version 2.0)
January 2011 (version 1.3)
December 2009 (Version 1.0)
August 2010
The Synergies plus Gram Negative panels contain antimicrobial agents that will report-when-ready together
with dried overnight antimicrobial agents.
The report-when-ready antimicrobial agents may report rapid results (4.5 - 12 hrs) or overnight results (16 - 20
hrs) and the dried overnight antimicrobial agents will report overnight results (16 - 20 hrs).
The report-when-ready antimicrobial agents can only be read rapidly (4.5 - 12 hrs) by the WalkAway SI or
WalkAway plus System. Manual reading of all antimicrobial agents must be performed at 16 20 hrs.
Synergies plus Gram Positive panels:
The Synergies plus Gram Positive panels contain antimicrobial agents that will report-when-ready.
The report-when-ready antimicrobial agents may report rapid results (4.5 - 12 hrs) or overnight results (16 - 18 hrs).
The report-when-ready antimicrobial agents can only be read rapidly (4.5 - 12 hrs) by the WalkAway SI or
WalkAway plus System. Manual reading of all antimicrobial agents must be performed at 16 - 20 hrs.
For all Beta-lactam antimicrobial agents, the predicted interpretation for staphylococci will be based on the
penicillin and/or Oxacillin MICs.
MICs will only be reported for staphylococci and/or enterococci. MICs will not be reported for streptococci.
Referenced from the CLSI M100-S22
For some organism groups excluded from Tables 2A through 2J, the CLSI guideline M45 Methods for
Antimicrobial Dilution and Disk Susceptibility Testing of Infrequently Isolated or Fastidious Bacteria provides
suggestions for standardized methods for susceptibility testing, including information about drug selection,
interpretation and QC. The organism groups covered in that document are Abiotrophia and Granulicatella spp.
(formerly known as nutritionally deficient or nutritionally variant streptococci); Aeromonas spp.; Bacillus spp.
(not B. anthracis), Campylobacter jejuni/coli, Corynebacterium spp. (including C. diptheriae); Erysipelothrix
rhusiopathiae, the HACEK group: Aggregatibacter spp. (formerly Haemophilus aphrophilus, H. paraphrophilus,
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9020-7493B
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Cefoxitin Screen
The Dried Cefoxitin Screen is intended to determine the susceptibility of staphylococci to the penicillinasestable beta-lactams, using the Cefoxitin Screen Well (CfxS) and the Oxacillin MIC result at 16/18 hours. The
CfxS result and Oxacillin MIC are read independently at 16/18 hours and then processed through the LabPro
software or interpreted manually to determine the final interpretation to the penicillinase-stable beta-lactams
(i.e., Oxacillin). The interpretation rules are shown in the following table:
CfxS
Oxacillin MIC
0.25
0.5
Oxacillin Interpretation
S. aureus or S. lugdunensis
Other CNS
S
S
S
S*
4 Neg
R Check mecA
1 or 2
S
(see comment)
>2
R
R
0.25
R*
R*
0.5
R*
R
> 4 Pos
1 or 2
R*
R
>2
R
R
Comment: CNS with CfxS 4 and Oxacillin MICs of 1 or 2 give variable mecA results. Perform mecA testing
if beta-lactam therapy is critical for patient care.
Interpretations of S* or R* are used by the LabPro software when the Cefoxitin Screen result changes the
interpretation of the Oxacillin MIC result. The LabPro software will flag CNS isolates when CfxS is negative
and Oxacillin MICs are 1 or 2 g/ml. The default interpretation will be R, however, mecA status is variable and
must be checked before these isolates are reported as Oxacillin susceptible (mecA negative only). These
criteria should also be followed when interpreting the results manually; however, the asterisk is not required.
For panels containing Oxacillin only: Staphylococci should be reported as resistant to Ampicillin, Amoxicillin/K
Clavulanate, Ampicillin/Sulbactam, Ertapenem, Imipenem, Meropenem, Penicillin, Piperacillin/Tazobactam,
Ticarcillin/K Clavulanate and the Cephalosporin antimicrobics (regardless of the MIC) when Oxacillin MICs are
>2 g/ml for S. aureus and S. lugdunensis and 0.5 g/ml for coagulase negative staphylococci other than S.
lugdunensis.
For panels containing both Oxacillin and the Cefoxitin Screen Well (CfxS): Staphylococci should be reported as
resistant to Ampicillin, Amoxicillin/K Clavulanate, Ampicillin/Sulbactam, Ertapenem, Imipenem, Meropenem,
Penicillin, Piperacillin/Tazobactam, Ticarcillin/K Clavulanate and the Cephalosporin antimicrobics (regardless of
the MIC) when CfxS is > 4 g/ml for all staphylococci or Oxacillin MICs are >2 g/ml for S. aureus and S.
lugdunensis or > 0.5 g/ml for other coagulase negative staphylococci. Based on MicroScan clinical studies, for
coagulase negative staphylococci other than S. lugdunensis when CfxS is 4 g/ml and Oxacillin MIC is 0.5,
the mecA status has been shown to be negative and the Oxacillin interpretation will be reported as S*. For
coagulase negative staphylococci other than S. lugdunensis when CfxS is 4 g/ml and Oxacillin MIC is 1 or 2,
mecA status is variable and must be checked before reporting these antimicrobial agents as susceptible.
Inducible Clindamycin
The Inducible Clindamycin test (ICd) is intended to detect inducible clindamycin resistance in staphylococci
intermediate or resistant to erythromycin and susceptible or intermediate to clindamycin. Expression of
resistance due to the erm gene may require induction by erythromycin. Results of ICd are equivalent to the Dzone disk approximation test. Reported for systemic sources only.
Tests
Negative
Positive
Inducible Clindamycin Test
4/0.5
> 4/0.5
- Staphylococci
When ICd is reported as Positive (>4/0.5) the clindamycin result will be reported as resistant (R*)
regardless of the MIC.
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1. MICroSTREP plus panels can report antimicrobial agent results for all streptococci: S. pneumoniae, betahemolytic streptococci, viridans streptococci and viridans streptococci (S. bovis group).
2. The Dried Overnight Gram-Positive panels can report antimicrobial agent results for beta-hemolytic
streptococci (S. agalactiae) and viridans streptococci (S. bovis) only.
3. Antimicrobial agent results for viridans streptococci (S. bovis) will be reported using viridans streptococci
breakpoints (CLSI and EUCAST).
4. Antimicrobial agent results for beta-hemolytic streptococci (S. agalactiae) will be reported using beta-hemolytic
streptococci breakpoints (CLSI) or Streptococcus groups A, B, C and G breakpoints (EUCAST).
5. Antimicrobial agent results for viridans streptococci (S. bovis) and beta-hemolytic streptococci (S.
agalactiae) will be reported using other streptococci breakpoints when using SFM interpretive guidelines.
Streptococci Limitations:
1. S. pneumoniae is contraindicated for use on the Antimicrobial Susceptibility Test (AST) portion of MicroScan
Dried Overnight Gram positive panels.
2. All streptococci, except beta-hemolytic streptococci (S. agalactiae) and viridans streptococci (S. bovis) are
For the Synergies plus Gram-Negative Panels, sufficient strains of Vibrio cholerae were not tested to establish
efficacy with Ampicillin, Chloramphenicol, Tetracycline and Trimethoprim/Sulfamethoxazole. Interpretive
breakpoints should not be reported.
Synergy Screen Reporting
Gentamicin Synergy Screen
1
(GmS) Reporting
Enterococci
500 = S, >500 = R
Streptococci
Do not report, drug, therapy
(S. agalactiae and
or MIC.
S. bovis group)
1
Based on CLSI M100-S22.
2
Based on French Market Center request in 1995.
9020-7493B
Streptomycin Synergy
Screen
(StS)
1
Reporting
1000 = S, >1000 = R
Do not report, drug, therapy
or MIC.
Kanamycin Synergy
Screen
(KSS )
2
Reporting
1000 = S, >1000 = R
1000 = S, >1000 = R
Page 10 of 158
Antimicrobial
Subclass
Amoxicillin
Ampicillin
Ureidopenicillin
Piperacillin
Carboxypenicillin Ticarcillin
-lactam/ Amoxicillin-clavulanate
lactamase
(Aug)
inhibitor
Ampicillin-sulbactam
combinations
Piperacillin-tazobactam
Ticarcillin-clavulanate
(Tim)
Cephems
Cefaclor
Cefazolin
Cefdinir
Cefepime
Cefotaxime
Cefpodoxime
Ceftriaxone
Cefuroxime
Cephalothin
Carbapenems
Ertapenem
Imipenem
Meropenem
An asterisk (*) will appear beside every predicted interpretation
9020-7493B
Aminopenicillin
Antimicrobial Agent
If
PenicillinS &
Oxacillin-S
S*
S*
S*
S*
S*
If
Penicillin-R &
Oxacillin-S
R*
R*
R*
R*
S*
If Penicillin-S or R
& Oxacillin-R
S*
S*
S*
S*
S*
S*
R*
R*
R*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
S*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
R*
Page 11 of 158
Dried Overnight Gram-Negative Panels and Synergies plus Gram-Negative Panels. The SCREEN for suspected
ESBL-producing organisms is for Escherichia coli, K. oxytoca, and K. pneumoniae only and utilizes cefpodoxime (1
or 4 g/ml, depending on panel type), aztreonam, cefotaxime, ceftazidime, ceftriaxone, ESBL-a (cefpodoxime at 1
or 4 g/ml depending on panel type) and ESBL-b (ceftazidime, 1 g/ml) as Screening agents. P. mirabilis utilizes
cefotaxime, ceftazidime and cefpodoxime (1 g/ml) as screening agents. Some antimicrobials used as screening
agents on the Dried Gram-Negative Panels are also present on the Synergies plus panels; however, only ESBL-a
and ESBL-b are used as screening agents for Synergies plus panels.
ESBL CONFIRMATION testing utilizes a comparison of MIC values obtained with ceftazidime to ceftazidime/ K.
clavulanate (4 g/ml), or cefotaxime to cefotaxime/ K. clavulanate (4 g/ml). Some older panels compare
ceftazidime to the BSE well (ceftazidime/ K. clavulanate (2 g/ml)). The MIC to the single antimicrobial must be 3
doubling dilutions greater than the MIC to the combination antimicrobial. If either comparison meets the criteria for
a positive result, the confirmation test will be positive. ESBL confirmation rules take precedence over ESBL
Screening rules in the software.
ESBL confirmation rules apply to the following members of the
Enterobacteriaceae: Citrobacter amalonaticus, C. koseri (diversus), C. farmeri, C. freundii complex, Citrobacter
species, Enterobacter aerogenes, E. cloacae, Escherichia coli, K. oxytoca, K. pneumoniae, Morganella morganii,
Proteus mirabilis, P. vulgaris, P. rettgeri, Salmonella species, and Serratia marcescens. The ESBL confirmation
test is being applied to more organisms than are included in the CLSI ESBL confirmation test and should not be
construed as being CLSI approved.
If the ESBL Screen is activated, the report generated for a suspected ESBL-producing strain of E. coli, K.
pneumoniae, K. oxytoca or P. mirabilis will report MIC values with normal SIR interpretations for all antimicrobial
agents tested. However, if elevated MIC values are obtained for one or more of the screening antimicrobial
agents, those agents giving the elevated MIC values will carry the interpretation EBL?
The report generated for a CONFIRMED ESBL-producing strain will still report MIC values for all antimicrobial
agents tested; however, the single or screening antimicrobial agents, including ESBL-a or ESBL-b, giving elevated
MIC values will carry the interpretation ESBL, while all other cephalosporins, penicillins and aztreonam will have
MIC values but will be given the interpretation R*.
The footnotes on the patient report corresponding to these interpretations are as follows:
EBL? indicates that a particular strain is a suspected ESBL. Confirmatory tests are needed to differentiate
ESBLs from other beta-lactamases.
ESBL indicates that a particular strain is a confirmed ESBL.
R* indicates resistance to cephalosporins, penicillins and aztreonam is due to confirmed extended-spectrum
beta-lactamases (ESBL).
These special interpretations will not appear if the laboratory chooses no when a suspected or confirmed ESBLproducer is flagged; normal SIR interpretative categories will be reported.
9020-7493B
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Interpretations Reported as ESBL? or ESBL for the following ESBL Screening Antimicrobial Agents:
Drug
MIC
Cefpodoxime
CPD1,3
0.5-1
1
1-4
1-4, 32
1-16
1, 4-8
1, 4-16
1, 8-16
1,8
2-16
4-16
4-32
8-16
0.5-2,16
1-16
1-32
1-64
1-2, 16
1-2, 8-16
1-2, 8-32
2-32
2-8, 32
2, 8-32
2, 16
4-32
4-8, 32
8-32
8,32
0.5-8
1-8
1-16
1-32
1, 4-8
1, 4-16
1, 8-16
1, 8
1-128
2-16
4-32
8-16
0.5-2
1-8
1-2, 8, 32
2-32
4-32
4-8, 32
8-32
8,32
4
>1
>1
>4
>2
>2
>4
>4
>8
>8
>4
>8
>8
>16
>2
>2
>2
>2
>2
>2
>2
>4
>4
8
>16
>8
>8
>16
>32
>2
>2
>2
>2
>4
>4
>8
>8
>2
>4
>8
>16
>2
>2
>2
>4
>8
8
>16
>32
>4
>1
Aztreonam
AZT
Cefotaxime
CFT
Ceftazidime
CAZ
Ceftriaxone
CAX
ESBL-a1,3
(Cefpodoxime)
ESBL-b,3
(Ceftazidime)
1. Panels containing a dilution of 4 g/ml Cefpodoxime will follow ESBL rules based on current CLSI
documents. Panels with dilutions of 1 g/ml or 1-2 g/ml Cefpodoxime will follow CLSI/NCCLS M100-S9.
2. Rapid results (<16 hrs) are not provided for ESBL-a and ESBL-b on Synergies plus Gram-Negative
panels. Results are available at 16-20 hours.
3. P. mirabilis utilizes Cefotaxime, Cefpodoxime at > 1 g/ml and Ceftazidime as screening agents.
9020-7493B
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CFZ
CPE
CFP
CFR
CDN
CFE
Cefuroxime
Cephalothin
Ceftizoxime
Ceftriaxone
CRM
CF
CZ
CAX
Penicillins
Amoxicillin
Ampicillin
Mecillinam
Mezlocillin
Piperacillin
Ticarcillin
AMX
AM
MEC
MZ
PI
TI
9020-7493B
AUG
A/S
C/S
P/T
TIM
Carbapenems
Imipenem
Meropenem
Ertapenem
Doripenem
IMP
MER
ETP
DOR
Cephamycins
Cefotetan
Cefoxitin
CTN
CFX
Page 14 of 158
NOTE: 1.
2.
3.
4.
5.
Amikacin
(Ak)
NOTE: 1.
2.
3.
4.
5.
6.
MIC
4.
NONENTEROBACTERIACEAE
PSEUDOMONAS
SPP.
ACINETOBACTER SPP.
>
R
R
R
R
32
R
I
R
R
16
I
S
I
I
8
S
S
S
S
4
S
S
S
S
2
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except for Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E, NM40, NUC56 and NUC69E
panels.
For Dried Overnight panels, do not report therapy for Salmonella/Shigella group because dangerously
misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia and Y. pestis.
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
PSEUDOMONAS
SPP.
ACINETOBACTER SPP.
>
R
R
R
R
16
I
S
I
I
8
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except for Acinetobacter spp. and Pseudomonas spp.) therapy based on
CLSI M100-S22.
Use for NBC45, NBC46, NM40, NUC56 and NUC69E panels.
For Dried Overnight panels, do not report therapy for Salmonella/Shigella group because dangerously
misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia and Y. pestis.
Based on CLSI M100-S22 interpretive guidelines for Non-Enterobacteriaceae, all MICs of >16 will report
as R, since these dilutions do not differentiate between I and R (S16, I=32, R64).
Amikacin (Ak)
NOTE: 1.
2.
3.
ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
R
32
R
R
R
16
I
I
I
8
S
S
S
4
S
S
S
2
S
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
For Dried Overnight panels, do not report therapy for Salmonella/Shigella group because dangerously
misleading results can occur.
Do not report therapy for Y. pestis.
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Page 15 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
32
I
I
I
16
S
S
S
8
S
S
S
4
S
S
S
2
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. For Dried Overnight panels, do not report therapy for Salmonella/Shigella group because dangerously
misleading results can occur.
3. Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia and Y. pestis.
Amikacin (Ak)
NOTE: 1.
2.
3.
4.
5.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
>
R
8
S
4
S
2
S
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Amoxicillin /
K Clavulanate (Aug)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
R
16
S
S
S
8
S
S
S
Therapy based on CLSI M100-S22.
Use for NUC69C panel
For Dried Overnight panels, do not report therapy for Salmonella/Shigella group because dangerously
misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia and Y. pestis. .
Based on CLSI M100-S22 interpretive guidelines for Enterobacteriaceae, Non-Enterobacteriaceae and
P. aeruginosa, all MICs of >16 will report as R, since these dilutions do not differentiate between I and R
(S16, I=32, R64).
Amoxicillin (Amx)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
16/8
R
8/4
S
4/2
S
2/1
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report drug, therapy or MIC for B. pseudomallei.
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Page 16 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16/8
I
8/4
S
4/2
S
2/1
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Y. pestis because dangerously misleading results can occur.
3. Do not report drug, therapy or MIC for B. pseudomallei.
Ampicillin (Am)
NOTE: 1.
2.
3.
4.
5.
2.
3.
4.
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
8
S
4
S
2
S
1
S
0.5
S
Enterobacteriaceae therapy based on EUCAST V3.1.
V. cholerae therapy based on CLSI M45-A2.
Use for NBC46, NM40 and NUC56 panels
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Based on CLSI interpretive guidelines for V. cholerae, all MICs of >8 will report
as N/R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
Ampicillin (Am)
NOTE: 1.
ENTEROBACTERIACEAE
>
R
16
R
8
S
Enterobacteriaceae therapy based on EUCAST V3.1.
V. cholerae therapy based on CLSI M45-A2.
Use for EUCAST Blended panel class except NBC46, NM40 and NUC56 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Ampicillin (Am)
NOTE: 1.
2.
3.
4.
5.
6.
MIC
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P. AERUGINOSA
V. CHOLERAE
R
I
S
V. CHOLERAE
N/R
S
S
S
S
S
V. CHOLERAE
>
R
R
16
I
I
8
S
S
4
S
S
2
S
S
Enterobacteriaceae therapy based on CLSI M100-S22 and V. cholerae therapy based on CLSI M45A2.
For Rapid fluorogenic panel MIC format, do not report drug, therapy or MIC for C. braakii/C. freundii/C.
sedlakii, C. werkmanii/C. youngae, C. amalonaticus/koseri group, Citrobacter species, Proteus/Providencia
group (except P. mirabilis) or Other Species group. See back of therapy guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp. and Plesiomonas shigelloides.
9020-7493B
Page 17 of 158
NOTE: 1.
2.
3.
4.
5.
5.
5.
6.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
V. CHOLERAE
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
(Acinetobacter spp. only).
PSEUDOMONAS SPP.
>
R
R
16/8
R
I
8/4
S
S
4/2
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae (Acinetobacter spp. only) therapy based on CLSI M100-S22.
Use for EUCAST Blended therapy panel class, except for NM40 panel.
Do not report drug, therapy or MIC for C. freundii group (See back of therapy guide for species names),
E. aerogenes, and E. cloacae.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Ampicillin-Sulbactam
(A/S)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
16
I
I
8
S
S
Enterobacteriaceae therapy based on CLSI M100-S22 and V. cholerae therapy based on CLSI M45-A2.
Use for panels with breakpoint format.
For Rapid fluorogenic panel breakpoint format, do not report drug, therapy or MIC for C. braakii/C.
freundii/C. sedlakii, C. werkmanii/C. youngae, C. amalonaticus/koseri group, Citrobacter species, P.
mirabilis or M. morganii. See back of therapy guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp. and Plesiomonas shigelloides.
Ampicillin-Sulbactam
(A/S)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
(Acinetobacter spp. only).
PSEUDOMONAS SPP.
>
R
R
8/4
S
S
4/2
S
S
2/1
S
S
1/0.5
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae (Acinetobacter spp. only) therapy based on CLSI M100-S22.
Use for NM40 panel.
Do not report drug, therapy or MIC for C. freundii group (See back of therapy guide for species names),
E. aerogenes, and E. cloacae.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on CLSI M100-S22 interpretive guidelines for Non-Enterobacteriaceae, all MICs of >8/4 will
report as R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
Ampicillin-Sulbactam
(A/S)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
(Acinetobacter spp. only)
P. AERUGINOSA
R
>
R
I
16/8
I
S
8/4
S
S
4/2
S
S
2/1
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Report CLSI therapy for Enterobacteriaceae and Acinetobacter spp. See back of therapy guide for
species names.
3. Do not report therapy for Y. pestis because dangerously misleading results can occur.
9020-7493B
Page 18 of 158
NOTE: 1.
2.
3.
4.
5.
6.
5.
6.
7.
5.
6.
7.
8.
9.
NON-ENTEROBACTERIACEAE.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE.
PSEUDOMONAS SPP.
>
R
R
R
16
R
I
I
8
R
S
I
1
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NC53, NM40 and NUC56 panels.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>4).
Aztreonam (Azt)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
R
16
R
I
I
8
R
S
I
4
I
S
I
2
I
S
I
1
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for NBC45, NC53, NM40 and NUC56 panels.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Aztreonam (Azt)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
8
R
S
I
1
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NBC45 panel.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>4).
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae (except Pseudomonas spp.), all MICs of
>8 will report as R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
Based on EUCAST interpretive guidelines for Pseudomonas spp., all MICs of >8 will report
as R, since these dilutions do not differentiate between I and R (S1, I=2-16, R>16).
9020-7493B
Page 19 of 158
NOTE: 1.
2.
3.
4.
5.
4.
5.
6.
5.
6.
7.
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
16
R
I
8
R
I
1
S
S
Therapy based on EUCAST V3.1.
Use for NUC57 panel.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>4).
Aztreonam (Azt)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
32
R
R
16
R
I
8
R
I
4
I
I
2
I
I
1
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class, except for NUC57 panel.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Vibrio spp.
Aztreonam (Azt)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
R
S
S
4
I
S
S
1
S
S
S
Enterobacteriaceae therapy based on ANVISA.
Non-Enterobacteriaceae and P. aeruginosa therapy based on CLSI M100-S22.
Use for NC66 panel.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and P. aeruginosa, all MICs of >8 will
report as R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
9020-7493B
Page 20 of 158
NOTE: 1.
2.
3.
4.
3.
4.
5.
5.
6.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
R
I
I
8
N/R
S
S
Therapy based on CLSI M100-S22.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried
Overnight panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 8 will report as N/R, since these
dilutions do not differentiate between S and I (S4, I=8, R16).
Aztreonam (Azt)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
R
32
R
R
R
16
R
I
I
8
I
S
S
4
S
S
S
2
S
S
S
1
S
S
S
Therapy based on CLSI M100-S22.
Aztreonam is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried
Overnight panels with E. coli, K. pneumoniae, and K. oxytoca. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Aztreonam (Azt)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
I
I
I
8
S
S
S
Therapy based on CLSI M100-S19.
Use for RNBC3 and RNUC1 panels.
For Rapid fluorogenic panel breakpoint format, do not report drug, therapy or MIC for P. aeruginosa.
Aztreonam is a screening antimicrobial agent for extended-spectrum beta-lactamases (ESBL). For Dried
Overnight panels and E. coli, K. oxytoca and K. pneumoniae see ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Cefazolin (Cfz)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
I
8
S
4
S
2
S
NOTE: 1. Therapy based on CLSI M100-S19.
2. For Rapid fluorogenic panel MIC and breakpoint format, do not report drug, therapy or MIC for C.
braakii/C. freundii/C. sedlakii, C. werkmanii/C. youngae, Citrobacter species, Proteus/Providencia
group (except P. mirabilis) or Other Species group. See back of therapy guide for species names.
3. Do not report therapy for Salmonella/Shigella group or Y. pestis because dangerously misleading
results can occur.
9020-7493B
Page 21 of 158
NOTE: 1.
2.
3.
4.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
16
R
I
R
8
R
S
S
4
I
S
S
2
I
S
S
1
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NC58, NC70E, NC71E and NM44E panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Cefepime (Cpe)
NOTE: 1.
2.
3.
4.
5.
6.
ENTEROBACTERIACEAE
>
N/R
4
S
2
S
Therapy based on CLSI M100-S19.
Use for NC63, NC68 and NC72 panels.
Do not report therapy for Salmonella/Shigella group or Y. pestis because dangerously misleading
results can occur.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs >4 will report as N/R, since these
dilutions do not differentiate between S, I and R (S8, I=16, R32).
Cefepime (Cpe)
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
8
R
S
S
4
I
S
S
2
I
S
S
1
S
S
S
0.5
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NBC46 NM40, NUC56 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs >8 will report as R, since these
dilutions do not differentiate between I and R (S8, I=16, R32).
Cefepime (Cpe)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
16
R
I
R
8
R
S
S
1
S
S
S
NOTE: 1. Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
2. Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
3. Use for NC53 and NUC59 panels.
4. Do not report therapy for Y. pestis because dangerously misleading results can occur.
5. Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
6. Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>4).
9020-7493B
Page 22 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
8
R
S
S
1
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NBC45 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>4).
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs >8 will report as R, since
these dilutions do not differentiate between I and R (S8, I=16, R32).
Cefepime (Cpe)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
32
R
R
8
R
S
4
I
S
2
N/R
S
Therapy based on EUCAST V3.1.
Use for NC48 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 2 will report as N/R,
since these dilutions do not differentiate between S and I (S1, I=2-4, R>4).
Cefepime (Cpe)
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
8
R
S
4
I
S
2
I
S
1
S
S
0.5
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for NM39 panel.
3. Do not report therapy for Y. pestis because dangerously misleading results can occur.
Cefepime (Cpe)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
8
R
S
1
S
S
Therapy based on EUCAST V3.1.
Use for NUC57 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>4).
9020-7493B
Page 23 of 158
NOTE: 1.
2.
3.
4.
5.
6.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
R
S
S
4
I
S
S
1
S
S
S
Enterobacteriaceae therapy based on ANVISA.
Non-Enterobacteriaceae and P. aeruginosa therapies based on CLSI M100-S22.
Use for NC66 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and P. aeruginosa, all MICs of >8 will
report as R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
Cefepime (Cpe)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
32
R
R
R
16
I
I
I
8
S
S
S
4
S
S
S
2
S
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Y. pestis because dangerously misleading results can occur.
3. Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Cefixime (Cfe)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
2
R
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Cefixime (Cfe)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
2
I
1
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Y. pestis because dangerously misleading results can occur.
3. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
9020-7493B
Page 24 of 158
NOTE: 1.
2.
3.
4.
3.
4.
5.
6.
7.
8.
3.
4.
5.
6.
7.
8.
9.
ACINETOBACTER SPP.
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
R
32
R
I
16
R
I
8
R
S
4
R
S
2
I
S
1
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae (including Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for EUCAST Blended panel class, except for NBC46, NC70E, NC71E, NM40, NUC56 and
NUC69E panels.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Based on CLSI M100-S22, do not report therapy for P. aeruginosa.
Cefotaxime (Cft)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
R
R
32
I
I
I
16
S
S
S
Therapy based on Manufacturers Breakpoints.
For Dried Overnight panels, do not report drug, therapy or MIC for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
For Dried Overnight panels, do not report therapy for Aeromonas spp, Plesiomonas shigelloides,
Vibrio spp. and Non-Enterobacteriaceae (except Acinetobacter spp. and P. aeruginosa).
Cefotaxime (Cft)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
N/R
16
R
I
8
R
S
4
R
S
2
I
S
1
S
S
0.5
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae (including Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for NBC46, NC70E, NM40, NUC56 and NUC69E panels.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Based on CLSI M100-S22, do not report therapy for P. aeruginosa.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >16 will report as N/R,
since these dilutions do not completely differentiate between I and R (S8, I=16-32, R64).
9020-7493B
Page 25 of 158
NOTE: 1.
2.
3.
4.
5.
5.
6.
3.
4.
5.
6.
7.
8.
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
32
R
8
R
4
R
2
N/R
Therapy based on EUCAST V3.1.
Use for NC48 panel.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on EUCAST interpretive criteria for Enterobacteriaceae, all MICs of 2 will report as N/R, since
these dilutions do not differentiate between S and I (S1, I=2, R>2).
Cefotaxime (Cft)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
16
R
2
I
1
S
0.5
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class, except for NC48 panel.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Cefotaxime (Cft)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
R
I
16
R
I
8
N/R
S
Therapy based on CLSI M100-S22.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Use for NC71C and NC71E panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Based on CLSI M100-S22, do not report therapy for P. aeruginosa.
Based on CLSI interpretive breakpoints for Enterobacteriaceae, all MICs of 8 will report as N/R, since
these dilutions do not differentiate between S, I and R (S1, I=2, R4).
9020-7493B
Page 26 of 158
NOTE: 1.
2.
3.
4.
5.
6.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
N/R
16
R
I
8
R
S
4
R
S
2
I
S
1
S
S
Therapy based on CLSI M100-S22.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Use for NC66, NC70C and NUC69C panels
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa and S. maltophilia.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >16 will report as N/R, since
these dilutions do not completely differentiate between I and R (S8, I=16-32, R64).
NOTE: 1.
2.
3.
4.
5.
6.
7.
Cefotaxime (Cft)
3.
4.
5.
6.
ENTEROBACTERIACEAE
>
R
R
64
R
R
32
R
I
16
R
I
8
R
S
4
R
S
2
I
S
1
S
S
Therapy based on CLSI M100-S22.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Based on CLSI M100-S22, do not report therapy for P. aeruginosa.
Cefotaxime (Cft)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
R
I
16
R
I
8
R
S
4
R
S
2
N/R
S
Therapy based on CLSI M100-S22.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa and S. maltophilia.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 2, will report as N/R, since these
dilutions do not differentiate between S and I (S1, I=2, R4).
9020-7493B
Page 27 of 158
NOTE: 1.
2.
3.
4.
5.
6.
3.
4.
5.
6.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
R
I
8
N/R
S
Therapy based on CLSI M100-S22.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa and S. maltophilia.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 8 will report as N/R, since these
dilutions do not differentiate between S and I (S1, I=2, R4).
Cefotaxime (Cft)
NOTE: 1.
2.
3.
4.
5.
ENTEROBACTERIACEAE
>
R
R
32
R
I
16
R
I
8
R
S
4
N/R
S
Therapy based on CLSI M100-S22.
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa and S. maltophilia.
Do not report drug, therapy or MIC for M. morganii and Serratia spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 4 will report as N/R, since these
dilutions do not differentiate between S and I (S1, I=2, R4).
Cefotaxime (Cft)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
16
I
I
8
S
S
4
S
S
Therapy based on CLSI M100-S19.
Use for RNBC3 and RNUC1 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Based on CLSI M100-S22, do not report therapy for P. aeruginosa.
Cefotaxime (Cft)
NOTE: 1.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
16
2
Cefotaxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca and P. mirabilis. See ESBL information in front of guide.
Page 28 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
16/4
8/4
4/4
2/4
1/4
0.5/4
0.25/4
NOTE: 1. Cefotaxime/4 K Clavulanate is a confirmation antimicrobial for extended-spectrum betalactamases (ESBL) on Dried Overnight panels. See ESBL information in front of guide.
Cefotetan (Ctn)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
32
I
16
S
8
S
4
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group or Y. pestis because dangerously misleading results can
occur.
3. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Cefoxitin (Cfx)
MIC
ENTEROBACTERIACEAE
>
32
8
4
2
NOTE: 1. Therapy based on SFM 2012.
2. Use for EUCAST panel class.
Cefoxitin (Cfx)
MIC
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
R
I
S
S
S
ENTEROBACTERIACEAE
>
R
32
R
16
I
8
S
4
S
2
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group or Y. pestis because dangerously misleading results can
occur.
9020-7493B
Page 29 of 158
NOTE: 1.
2.
3.
4.
5.
6.
3.
4.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
1
S
0.5
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended panel class, except for NBC46 panel.
Do not report drug, therapy or MIC for S. marcescens.
Cefpodoxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Cefpodoxime (Cpd)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
8
S
Therapy based on CLSI M100-S22.
Use for NBC49C, NBC49E, NBC42, NBC46 and NUC56 panels.
Do not report therapy for Salmonella/Shigella group or Y. pestis because dangerously misleading results can
occur.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of >8 will report as R, since these
dilutions do not differentiate between I and R (S8, I=16, R32).
Cefpodoxime (Cpd)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
4
I
2
S
1
S
Therapy based on CLSI M100-S22.
Cefpodoxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Cefpodoxime (Cpd)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
1
NOTE: 1. Cefpodoxime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. pneumoniae, K. oxytoca, and P. mirabilis . See ESBL information in front of guide.
2. Use for NBC46 panel.
Cefsulodin (Cfs)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
32
8
NOTE: 1. Therapy based on SFM 2012.
9020-7493B
Page 30 of 158
NOTE: 1.
2.
3.
4.
5.
3.
4.
5.
6.
7.
3.
4.
5.
6.
B. PSEUDOMALLEI
NONPSEUDOMONAS SPP.
ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
B. PSEUDOMALLEI
>
R
R
R
N/R
8
R
S
S
S
4
I
S
S
S
2
I
S
S
S
1
S
S
S
S
0.5
S
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp. and B. pseudomallei) including Acinetobacter spp.
therapy based on CLSI M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
Use for NBC46, NC70E, NM40 and NUC56 panels.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae all MICs >8 will report as R, since these
dilutions do not differentiate between I and R (S8, I=16, R>32).
Based on CLSI interpretive guidelines for B. pseudomallei, all MICs >8 will report as N/R, since these dilutions
do not differentiate between I and R (S8, I=16, R32).
Ceftazidime (Caz)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
R
R
R
32
R
R
R
R
16
R
I
R
I
8
R
S
S
S
4
I
S
S
S
2
I
S
S
S
1
S
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp. and B. pseudomallei) including Acinetobacter spp.
therapy based on CLSI M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NC70E, NM40 and NUC56 panels.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Ceftazidime (Caz)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
B. PSEUDOMALLEI
>
N/R
R
R
R
16
N/R
I
R
I
8
N/R
S
S
S
1
S
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp. and B. pseudomallei) including Acinetobacter spp.
therapy based on CLSI M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
Use for NBC45 panel.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs >1 will report as N/R, since
these dilutions do not differentiate between I and R (S1, I=2-4, R>8).
9020-7493B
Page 31 of 158
NOTE: 1.
2.
3.
4.
3.
4.
5.
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
32
R
R
16
R
R
8
R
S
4
I
S
2
I
S
1
S
S
0.5
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Ceftazidime (Caz)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
ACINETOBACTER SPP.
P. AERUGINOSA
B.PSEUDOMALLE
I
>
R
R
R
R
16
R
I
I
I
8
R
S
S
S
4
I
S
S
S
1
S
S
S
S
Enterobacteriaceae therapy based on ANVISA.
Non-Enterobacteriaceae and P. aeruginosa therapies based on CLSI M100-S22 and B. pseudomallei
therapy based on CLSI M45-A2.
Use for NC66 panel.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Ceftazidime (Caz)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
R
128
R
R
R
R
64
R
R
R
R
32
R
R
R
R
16
R
I
I
I
8
I
S
S
S
4
S
S
S
S
2
S
S
S
S
1
S
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
2. Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
3. Do not report therapy for Y. pestis because dangerously misleading results can occur.
9020-7493B
Page 32 of 158
NOTE: 1.
2.
3.
4.
5.
6.
3.
4.
4.
NON-ENTEROBACTERIACEAE P. AERUGINOSA
B. PSEUDOMALLEI
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
R
16
R
I
I
I
8
N/R
S
S
S
Therapy based on CLSI M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 8 will report as N/R, since
these dilutions do not differentiate between S and I (S4, I=8, R16).
Ceftazidime (Caz)
NOTE: 1.
2.
3.
ENTEROBACTERIACEAE
>
R
R
R
N/R
8
I
S
S
S
4
S
S
S
S
2
S
S
S
S
1
S
S
S
S
Therapy based on CLSI M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
Use for NC70C panel.
Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and P. aeruginosa, all MICs of >8
will report as R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
Based on CLSI interpretive guidelines for B. pseudomallei, all MICs of >8 will report as N/R, since these
dilutions do not differentiate between I and R (S8, I=16, R32).
Ceftazidime (Caz)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
R
16
I
I
I
I
8
S
S
S
S
4
S
S
S
S
2
S
S
S
S
Therapy based on CLSI M100-S19 and B. pseudomallei therapy based on CLSI M45-A2.
Use for RNUC1 panel.
For Rapid fluorogenic panel MIC format, do not report drug, therapy or MIC for P. mirabilis and M.
morganii.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Ceftazidime (Caz)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
16
I
I
I
8
S
S
S
NOTE: 1. Therapy based on CLSI M100-S19 and B. pseudomallei therapy based on CLSI M45-A2.
2. Use for RNBP3 panels.
3. Do not report therapy for Y. pestis because dangerously misleading results can occur.
9020-7493B
R
I
S
Page 33 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
8
1
NOTE: 1. Ceftazidime is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of guide.
2. Use for NC67 panel.
Ceftazidime-K
Clavulanate (Caz/CA)
MIC
Ceftizoxime (Cz)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
32/4
16/4
8/4
4/4
2/4
1/4
0.5/4
0.25/4
NOTE: 1. Ceftazidime/4 g/ml K Clavulanate is a confirmation antimicrobial for extended-spectrum betalactamases (ESBL) on Dried Overnight panels. See ESBL information in front of therapy guide.
NOTE: 1.
2.
3.
4.
5.
6.
7.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
8
S
S
Therapy based on CLSI M100-S19.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia and Vibrio spp.
Do not report therapy for P. aeruginosa.
Ceftriaxone (Cax)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS
SPP.
>
R
N/R
2
I
S
1
S
S
0.5
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Ceftriaxone is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried
Overnight panels with E. coli, K. oxytoca and K. pneumoniae. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa, S. maltophilia, and Vibrio spp.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs >2 will report as N/R since
these dilutions do not differentiate between S, I and R (S8, I=16-32, R64).
9020-7493B
Page 34 of 158
NOTE: 1.
2.
3.
4.
3.
4.
5.
6.
3.
4.
5.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
N/R
8
R
S
4
R
S
2
I
S
1
S
S
Therapy based on CLSI M100-S22.
Ceftriaxone is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca and K. pneumoniae. See ESBL information in front of therapy guide.
Use for NC67 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa, S. maltophilia, and Vibrio spp.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >8 will report as N/R,
since these dilutions do not differentiate between I and R (S8, I=16-32, R64).
Ceftriaxone (Cax)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
R
32
R
I
8
R
S
2
I
S
1
S
S
Therapy based on CLSI M100-S22.
Ceftriaxone is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca and K. pneumoniae. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa, S. maltophilia, and Vibrio spp.
Ceftriaxone (Cax)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
R
I
16
R
I
8
R
S
4
R
S
2
N/R
S
Therapy based on CLSI M100-S22.
Ceftriaxone is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca and K. pneumoniae. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa, S. maltophilia, and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 2 will report as N/R, since
these dilutions do not differentiate between S and I (S1, I=2, R4).
9020-7493B
Page 35 of 158
NOTE: 1.
2.
3.
4.
5.
3.
4.
5.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
R
I
16
R
I
8
R
S
4
N/R
S
Therapy based on CLSI M100-S22.
Ceftriaxone is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca and K. pneumoniae. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa, S. maltophilia, and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 4 will report as N/R, since
these dilutions do not differentiate between S and I (S1, I=2, R4).
Ceftriaxone (Cax)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
R
I
16
R
I
8
N/R
S
Therapy based on CLSI M100-S22.
Ceftriaxone is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight
panels with E. coli, K. oxytoca and K. pneumoniae. See ESBL information in front of therapy guide.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, P. aeruginosa, S. maltophilia, and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 8 will report as N/R, since
these dilutions do not differentiate between S and I (S1, I=2, R4).
Ceftriaxone (Cax)
NOTE: 1.
2.
3.
4.
5.
9020-7493B
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
16
I
I
8
S
S
4
S
S
Therapy based on CLSI M100-S19.
Use for RNUC1 panel.
For Rapid fluorogenic panel MIC format, do not report drug, therapy or MIC for P. aeruginosa.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia, and Vibrio spp.
Ceftriaxone (Cax)
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
8
S
S
Therapy based on CLSI M100-S19.
Use for RNBP3 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia, and Vibrio spp.
Based on CLSI M100-S22, do not report therapy for P. aeruginosa.
Page 36 of 158
NOTE: 1.
2.
3.
4.
3.
4.
4.
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
I
8
S
4
S
2
S
1
S
Therapy based on CLSI M100-S22.
For Rapid fluorogenic panel MIC format, do not report drug, therapy or MIC for Proteus/Providencia group
(except P. mirabilis) or Other Species groups. See back of therapy guide for species names.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading results
can occur.
The CLSI breakpoints for Cefuroxime axetil (oral) are S4, I=8-16, R32.
NOTE: 1.
2.
3.
ENTEROBACTERIACEAE
>
R
16
R
8
S
4
S
2
S
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Report therapy for E. coli, P. mirabilis, and Klebsiella spp. only.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading
results can occur.
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
I
8
S
Therapy based on CLSI M100-S22.
Use for NC66, NC70C and NUC69C panels.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading results can
occur.
The CLSI breakpoints for Cefuroxime axetil (oral) and Enterobacteriaceae are S4, I=8-16, R32;
based on these breakpoints, panel dilutions do not differentiate between S and I.
Cephalothin (Cf)
MIC
ENTEROBACTERIACEAE
>
32
16
8
NOTE: 1. Therapy based on SFM 2012.
2. Use for EUCAST panel class.
9020-7493B
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
R
I
I
S
Page 37 of 158
NOTE: 1.
2.
3.
4.
MIC
5.
6.
3.
4.
5.
6.
3.
4.
5.
6.
7.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P.
AERUGINOSA
V. CHOLERAE
Y. PESTIS
>
R
R
R
16
R
I
I
8
S
S
S
Enterobacteriaceae (except Y. pestis) therapy based on EUCAST V3.1.
Non-Enterobacteriaceae therapy based on CLSI M100-S22 and V. cholerae and Y. pestis therapies
based on CLSI M45-A2.
Use for NM44E panel.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for E. cloacae, M. morganii, P. mirabilis and S. marcescens.
Do not report therapy for Acinetobacter spp. and B. pseudomallei.
ChloramphenicoI (C)
NOTE: 1.
2.
P. AERUGINOSA
>
N/R
8
S
Therapy based on CLSI M100-S22.
Use for NUC56 panel.
Report for urine sources only.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading
results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of >8 will report as N/R, since
these dilutions do not differentiate between I and R (S8, I=16, R32).
Chloramphenicol (C)
NOTE: 1.
2.
NON-ENTEROBACTERIACEAE
>
R
16
I
8
S
4
S
2
S
Therapy based on CLSI M100-S22.
Report for urine sources only.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading
results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Cephalothin (Cf)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P.
AERUGINOSA
V.
CHOLERAE
R
I
S
Y. PESTIS
>
R
N/R
N/R
N/R
8
S
S
S
S
Enterobacteriaceae (except Y. pestis) therapy based on EUCAST V3.1.
Non-Enterobacteriaceae therapy based on CLSI M100-S22 and V. cholerae and Y. pestis therapies
based on CLSI M45-A2.
Use for NBC46 and NM40 panels.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for E. cloacae, M. morganii, P. mirabilis and S. marcescens.
Do not report therapy for Acinetobacter spp. and B. pseudomallei.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, V. cholerae and Y. pestis, all MICs
of >8 will report as N/R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
9020-7493B
Page 38 of 158
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P.
AERUGINOSA
V. CHOLERAE
Y. PESTIS
>
R
R
R
R
16
I
I
I
I
8
S
S
S
S
4
S
S
S
S
NOTE: 1. Enterobacteriaceae (except V. cholerae and Y. pestis) and Non-Enterobacteriaceae therapies based on CLSI
M100-S22 and V. cholerae and Y. pestis therapies based on CLSI M145-A2.
2. Only systemic therapy will be reported.
3. Do not report therapy for Acinetobacter spp., B. pseudomallei and Vibrio spp.
Cinoxacin (Cn)
NOTE: 1.
2.
3.
4.
5.
3.
4.
5.
3.
4.
5.
6.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
Y. PESTIS
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS
SPP.
Y. PESTIS
>
R
R
R
2
R
I
R
1
I
S
I
0.5
S
S
S
Enterobacteriaceae (except Y. pestis) and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) including Acintobacter spp. therapy based on
CLSI M100-S22 and Y. pestis therapy based on CLSI M100-S17.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E (use CLSI M100-S21
breakpoints), NM40 and NUC56 panels.
Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Panel dilutions do not allow reporting of EUCAST breakpoints for Salmonella spp.
Ciprofloxacin (Cp)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
N/R
16
S
Therapy based on CLSI M100-S22.
Use for RNB3 panel.
Only urine therapy will be reported.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of >16 will report as N/R, since
these dilutions do not differentiate between I and R (S16, I=32, R64).
Ciprofloxacin (Cp)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
PSEUDOMONAS
SPP.
R
I
S
S
Y. PESTIS
>
R
N/R
R
N/R
1
I
S
I
S
0.5
S
S
S
S
Enterobacteriaceae (except Y. pestis) and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy including Acintobacter spp. based on
CLSI M100-S22 and Y. pestis therapy based on CLSI M100-S17.
Use for NBC45, NBC46, NM40 and NUC56 panels.
Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Panel dilutions do not allow reporting of EUCAST breakpoints for Salmonella spp.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and Y. pestis, all MICs of >1 will
report as N/R, since these dilutions do not differentiate between I and R (S1, I=2, R4).
9020-7493B
Page 39 of 158
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
>
R
2
R
1
I
0.5
S
0.25
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report drug, therapy or MIC for Acinetobacter spp.
Panel dilutions do not allow reporting of EUCAST breakpoints for Salmonella spp.
Ciprofloxacin (Cp)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
R
4
R
R
2
I
I
1
S
S
0.5
S
S
0.12
S
S
NOTE: 1. Therapy based on CLSI M100-S21.
2. Therapy for Y. pestis based on CLSI M100-S17.
3. Do not report therapy for B. cepacia, B. pseudomallei, and S. maltophilia.
Colistin (Cl)
NOTE: 1.
2.
3.
4.
MIC
5.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
R
R
I
S
S
P. AERUGINOSA
R
R
I
S
S
S
Y. PESTIS
R
R
I
S
S
S
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
4
R
S
2
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Use for EUCAST Blended panel class, except for NM40 panel.
Do not report therapy for Y. pestis.
Do not report drug, therapy or MIC for Salmonella species, E. cloacae, Acinetobacter species or Other
Non-Enterobacteriaceae (except Pseudomonas spp).
Colistin (Cl)
NOTE: 1.
2.
3.
4.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
2
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Use for NM40 panel.
Do not report therapy for Y. pestis.
Based on EUCAST interpretive guidelines for Pseudomonas spp., all MICs >2 will report as R, since
these dilutions do not differentiate between S and R (S4, R>4).
Do not report drug, therapy or MIC for Salmonella species, E. cloacae, Acinetobacter species or Other
Non-Enterobacteriaceae (except Pseudomonas spp).
9020-7493B
Page 40 of 158
NOTE: 1.
2.
3.
4.
MIC ENTEROBACTERIACEAE
5.
MIC
MIC
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
P. AERUGINOSA
>
R
R
4
R
I
2
S
S
Enterobacteriaceae therapy based on ANVISA.
P. aeruginosa therapy based on CLSI M100-S22.
Use for NC66 panel.
Do not report therapy for B. cepacia, S. maltophilia and Y. pestis.
Do not report drug, therapy or MIC for Salmonella species, E. cloacae, Acinetobacter species or Other
Non-Enterobacteriaceae.
Colistin (Cl)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
P. AERUGINOSA
>
4
2
Therapy based on CLSI M100-S22.
Do not report therapy for B. cepacia, S. maltophilia and Y. pestis.
Do not report drug, therapy or MIC for Acinetobacter species or Other Non-Enterobacteriaceae.
NOTE: 1.
2.
3.
Doripenem (Dor)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
2
S
S
Therapy based on EUCAST V3.1.
Use for NM39 panel.
Do not report therapy for Y. pestis.
Based on EUCAST interpretive guidelines for Pseudomonas spp., all MICs of >2 will report as R, since
these dilutions do not differentiate between S and R (S4, R>4).
Do not report drug, therapy or MIC for Salmonella species, E. cloacae or Acinetobacter species.
Colistin (Cl)
NOTE: 1.
2.
3.
4.
5.
PSEUDOMONAS SPP.
>
R
R
4
R
S
2
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class, except for NM39 panel.
Do not report therapy for Y. pestis.
Do not report drug, therapy or MIC for Salmonella species, E. cloacae or Acinetobacter species.
Colistin (Cl)
NOTE: 1.
2.
3.
4.
ACINETOBACTER SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
R
I
S
PSEUDOMONAS SPP.
>
R
R
R
4
I
I
I
2
I
I
I
1
S
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report drug, therapy, or MIC for Aeromonas spp., Plesiomonas shigelloides, and Vibrio spp.
(including V. cholerae).
9020-7493B
Page 41 of 158
NOTE: 1.
2.
3.
4.
4.
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
4
R
2
R
1
I
0.5
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Vibrio spp.
Ertapenem (Etp)
NOTE: 1.
2.
3.
4.
NON-ENTEROBACTERIACEAE
>
R
R
2
I
S
1
S
S
0.5
S
S
Therapy based on CLSI M100-S22.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on CLSI interpretive guidelines for P. aeruginosa, all MICs of >2 will report as R, since these
dilutions do not differentiate between I and R (S2, I=4, R 8).
Do not report drug, therapy, or MIC for Aeromonas spp., Plesiomonas shigelloides, and Vibrio spp.
(including V. cholerae).
Ertapenem (Etp)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
4
R
I
2
I
S
1
S
S
Therapy based on CLSI M100-S22.
Use for NM44C and NC71C panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report drug, therapy, or MIC for Aeromonas spp., Plesiomonas shigelloides, and Vibrio spp.
(including V. cholerae).
Doripenem (Dor)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
1
I
0.5
S
Therapy based on ANVISA.
Use for NC66 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Vibrio spp.
9020-7493B
Page 42 of 158
Ertapenem (Etp)
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
4
R
2
R
1
N/R
Therapy based on CLSI M100-S22.
Use for NBC43, NBC44, NBC47, NM38, NUC55, NUC60, NUC61 and NUC62 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Enterobacteriaceae that are resistant to extended spectrum cephalosporins (3rd generation) and have
Ertapenem MICs of >1 may produce KPC-type or other carbapenemases. The isolate should be saved
and results verified by repeat testing unless patient had isolate previously. Follow current CLSI or
public health guidelines. Infectious Disease Consult suggested.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 1 will report as N/R, since
these dilutions do not differentiate between S and I (S0.5, I=1, R2).
NOTE: 1.
2.
3.
4.
5.
6.
Ertapenem (Etp)
6.
ENTEROBACTERIACEAE
>
R
4
R
2
R
1
I
0.5
S
Therapy based on CLSI M100-S22.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Enterobacteriaceae that are resistant to extended spectrum cephalosporins (3rd generation) and have
Ertapenem MICs of >1 may produce KPC-type or other carbapenemases. The isolate should be saved
and results verified by repeat testing unless patient had isolate previously. Follow current CLSI or
public health guidelines. Infectious Disease Consult suggested.
NOTE: 1.
2.
3.
4.
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
4
R
2
N/R
Therapy based on CLSI M100-S22.
Use for NBC33, NBC34, NBC39, NBC41, NBC42, NC39, NC50, NUC45 and NUC51 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Enterobacteriaceae that are resistant to extended spectrum cephalosporins (3rd generation) and have
Ertapenem MICs of >1 may produce KPC-type or other carbapenemases. The isolate should be saved
and results verified by repeat testing unless patient had isolate previously. Follow current CLSI or
public health guidelines. Infectious Disease Consult suggested.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 2 will report as N/R, since
these dilutions do not differentiate between S and I (S0.5, I=1, R2).
9020-7493B
Page 43 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
1
NOTE: 1. Therapy based on CLSI M100-S22.
2. Use for NUC52 panel.
3. Per CLSI, Enterobacteriaceae that are resistant to extended spectrum cephalosporins (3rd generation)
and have Ertapenem MICs of >1 may produce KPC-type or other carbapenemases. The isolate should
be saved and results verified by repeat testing unless patient had isolate previously. Follow current
CLSI or public health guidelines. Infectious Disease Consult suggested.
ESBL-a (ESa)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P. AERUGINOSA
>
4
NOTE: 1. ESBL-a is Cefpodoxime.
2. ESBL-a is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight panels
with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of the guide.
ESBL-b (ESb)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P. AERUGINOSA
>
1
NOTE: 1. ESBL-b is Ceftazidime.
2. ESBL-b is a screening antimicrobial for extended-spectrum beta-lactamases (ESBL) on Dried Overnight panels
with E. coli, K. oxytoca, K. pneumoniae, and P. mirabilis. See ESBL information in front of the guide.
Fosfomycin (Fos)
NOTE: 1.
2.
3.
4.
4.
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
64
R
32
S
16
S
Therapy based on EUCAST V3.1.
Use for EUCAST blended, EUCAST panel classes and NBC42, NBC43, NC54 and NM37 panels.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp., and Y. pestis.
Anecdotal evidence suggests that infections caused by wild type isolates of Pseudomonas spp. (ECOFF:
WT128mg/L) may be treated with combination of fosfomycin and other agents.
Fosfomycin (Fos)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
64
N/R
Therapy based on EUCAST V3.1.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp., and Y. pestis.
Anecdotal evidence suggests that infections caused by wild type isolates of Pseudomonas spp. (ECOFF:
WT128mg/L) may be treated with combination of fosfomycin and other agents.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 64 will report as N/R, since
these dilutions do not differentiate between S and R (S32, R>32).
9020-7493B
Page 44 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
4
I
2
S
NOTE: 1. Therapy based on FDA approved breakpoints.
2. For Dried Overnight panels, do not report drug, therapy or MIC for Non-Enterobacteriaceae and P.
aeruginosa.
3. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp., and Y. pestis.
Gemifloxacin (Gem)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
0.5
I
0.25
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp., and Y. pestis.
Gentamicin
(Gm)
NOTE: 1.
2.
3.
4.
5.
2.
3.
4.
5.
6.
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
PSEUDOMONAS
SPP.
Y. PESTIS
>
R
R
R
R
R
8
R
I
R
R
I
4
I
S
S
S
S
2
S
S
S
S
S
1
S
S
S
S
S
Enterobacteriaceae (except Y. pestis), Acinetobacter spp. and Pseudomonas spp. therapies based on
EUCAST.
Non-Enterobacteriaceae (except Pseudomonas spp. and Acinetobacter spp.) therapy based on CLSI
M100-S22 and Y. pestis therapy based on M45-A2.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E (use CLSI M100-S22
breakpoints), NM40 and NUC56 panels.
Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Gentamicin
(Gm)
NOTE: 1.
MIC
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
PSEUDOMONAS
SPP.
Y. PESTIS
>
R
R
R
R
R
4
I
S
S
S
S
2
S
S
S
S
S
Enterobacteriaceae (except Y. pestis), Acinetobacter spp. and Pseudomonas spp. therapies based on
EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp. and Acinetobacter spp.) therapy based on CLSI
M100-S22 and Y. pestis therapy based on M45-A2.
Use for NBC45, NBC46, NM40 and NUC56 panels.
Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and Y. pestis, all MICs of >4 will
report as R, since these dilutions do not differentiate between S and I (S4, I=8, R16).
9020-7493B
Page 45 of 158
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
R
8
R
R
R
4
I
S
S
2
S
S
S
1
S
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class.
3. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
Gentamicin (Gm)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
Y. PESTIS
>
R
R
R
R
8
I
I
I
I
4
S
S
S
S
2
S
S
S
S
1
S
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
3. Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Imipenem
(Imp)
NOTE: 1.
2.
3.
4.
5.
6.
MIC
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
PSEUDOMONAS
SPP.
B. PSEUDOMALLEI
>
R
R
R
R
R
8
I
I
I
I
4
I
S
S
S
2
S
S
S
S
1
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Acinetobacter spp and Pseudomonas spp.) therapy based on CLSI
M100-S22 and B. pseudomallei therapy based on CLSI M45-A2.
Use for EUCAST Blended panel class.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
For Dried Overnight panels, do not report therapy for B. cepacia and S. maltophilia.
Imipenem (Imp)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
R
8
I
I
4
I
S
2
S
S
1
S
S
0.5
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
9020-7493B
Page 46 of 158
NOTE: 1.
2.
3.
4.
5.
6.
4.
5.
4.
5.
6.
NONENTEROBACTERIACEAE
P.
AERUGINOSA
B. PSEUDOMALLEI
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P.
AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
R
8
R
I
R
I
4
R
S
I
S
2
I
S
S
S
1
S
S
S
S
Therapy based on CLSI M100-S22.
For Rapid fluorogenic panels, do not report drug, therapy or MIC for all gram-negative organisms.
For Dried Overnight panels, do not report therapy for Y. pestis because dangerously misleading results can
occur.
For Dried Overnight panels, do not report therapy for B. cepacia, S. maltophilia, Aeromonas spp.,
Plesiomonas shigelloides and Vibrio spp.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
Imipenem (Imp)
NOTE: 1.
2.
3.
ENTEROBACTERIACEAE
>
R
R
R
R
8
R
I
R
I
4
R
S
I
S
2
I
S
S
S
1
S
S
S
S
Enterobacteriaceae therapy based on ANVISA.
Non-Enterobacteriaceae and P. aeruginosa therapies based on CLSI M100-S22 and B. pseudomallei
therapy based on CLSI M45-A2.
Use for NC66 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and S. maltophilia, Aeromonas spp., Plesiomonas shigelloides and
Vibrio spp.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
Imipenem (Imp)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P.
AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
R
8
R
I
R
I
4
R
S
I
S
2
N/R
S
S
S
Therapy based on CLSI M100-S22.
For Rapid fluorogenic panels, do not report drug, therapy or MIC for all gram-negative organisms.
For Dried Overnight panels, do not report therapy for Y. pestis because dangerously misleading results can
occur.
For Dried Overnight panels, do not report therapy for B. cepacia, S. maltophilia, Aeromonas spp.,
Plesiomonas shigelloides and Vibrio spp.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 2 will report as N/R, since
these dilutions do not differentiate between S and I (S1, I=2, R4).
9020-7493B
Page 47 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
3.
4.
3.
4.
5.
NONENTEROBACTERIACEAE
P.
AERUGINOSA
B. PSEUDOMALLEI
MIC
ENTEROBACTERIACEAE NON-ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
R
R
4
R
I
R
R
2
I
S
I
I
1
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E, NM40 and NUC56
panels.
Do not report therapy for B. pseudomallei and Y. pestis.
Levofloxacin (Lvx)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
R
R
R
8
R
I
R
I
4
N/R
S
N/R
S
Therapy based on CLSI M100-S22.
For Rapid fluorogenic panels, do not report drug, therapy or MIC for all gram-negative organisms.
For Dried Overnight panels, do not report therapy for Y. pestis because dangerously misleading results can
occur.
For Dried Overnight panels, do not report therapy for B. cepacia, S. maltophilia, Aeromonas spp.,
Plesiomonas shigelloides and Vibrio spp.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 4 will report as N/R, since
these dilutions do not differentiate between S, I and R (S1, I=2, R4).
Based on CLSI interpretive guidelines for P. aeruginosa, all MICs of 4 will report as N/R, since these
dilutions do not differentiate between S and I (S2, I=4, R8).
Levofloxacin (Lvx)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE NON-ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
R
R
2
I
S
I
I
1
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for NBC45, NBC46, NM40 and NUC56 panels.
Do not report therapy for B. pseudomallei and Y. pestis.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >2 will report as R,
since these dilutions do not differentiate between S, I and R (S2, I=4, R8).
Levofloxacin (Lvx)
NOTE: 1.
2.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
4
I
2
S
1
S
0.5
S
Therapy based on CLSI M100-S22.
Do not report therapy for B. pseudomallei and Y. pestis.
R
I
S
S
S
P. AERUGINOSA
R
I
S
S
S
Page 48 of 158
NOTE: 1.
2.
3.
4.
5.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
8
S
Therapy based on EUCAST V3.1.
Use for EUCAST blended and EUCAST panel classes.
Only urine therapy will be reported.
For Dried Overnight panels, do not report drug, therapy or MIC for Klebsiella spp.
Do not report therapy for Y. pestis.
Meropenem (Mer)
NOTE: 1.
2.
3.
4.
5.
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
PSEUDOMONAS
SPP.
>
R
R
R
R
8
I
I
I
I
4
I
S
I
I
2
S
S
S
S
1
S
S
S
S
0.5
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for EUCAST Blended panel class.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. pseudomallei and S. maltophilia.
Meropenem (Mer)
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
R
I
R
4
R
S
I
2
I
S
S
1
S
S
S
Enterobacteriaceae therapy based on ANVISA.
Non-Enterobacteriaceae and P aeruginosa therapies based on CLSI M100-S22.
Use for NC66 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. pseudomallei and S. maltophilia.
Meropenem (Mer)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
R
I
R
4
R
S
I
2
I
S
S
1
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Y. pestis because dangerously misleading results can occur.
3. Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides, S. maltophilia,
and Vibrio spp.
9020-7493B
Page 49 of 158
NOTE: 1.
2.
3.
4.
5.
4.
4.
5.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
R
R
R
8
R
I
R
4
R
S
I
2
N/R
S
S
Therapy based on CLSI M100-S22.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides, S. maltophilia,
and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 2 will report as N/R, since
these dilutions do not differentiate between S, I and R (S1, I=2, R4).
Meropenem (Mer)
NOTE: 1.
2.
3.
ENTEROBACTERIACEAE
>
R
R
R
8
R
I
R
4
R
S
I
1
S
S
S
Therapy based on CLSI M100-S22.
Use for NBC42 and NBC43 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides, S. maltophilia,
and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of >1 will report as R, since
these dilutions do not differentiate between I and R (S1, I=2, R4).
Meropenem (Mer)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
R
I
R
4
N/R
S
N/R
Therapy based on CLSI M100-S22.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides, S. maltophilia,
and Vibrio spp.
Based on CLSI interpretive guidelines for Enterobacteriaceae, all MICs of 4 will report as N/R, since
these dilutions do not differentiate between S, I and R (S1, I=2, R4).
Based on CLSI interpretive guidelines for P. aeruginosa, all MICs of 4 will report as N/R, since these
dilutions do not differentiate between S and I (S2, I=4, R8).
9020-7493B
Page 50 of 158
NOTE: 1.
2.
3.
4.
5.
6.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
S
32
I
I
S
16
S
S
S
8
S
S
S
Therapy based on CLSI M100-S21.
For Rapid fluorogenic panel MIC format, do not report drug, therapy or MIC for Serratia group. See back of
therapy guide for species names.
For Dried Overnight panels, do not report drug, therapy or MIC for S. maltophilia.
For Rapid fluorogenic panels, do not report therapy for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides and Vibrio
spp.
Minocycline (Min)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
8
I
I
4
S
S
2
S
S
1
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides, Vibrio spp, and Y.
pestis.
Moxifloxacin (Mxf)
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
R
>
2
R
1
I
0.5
S
Therapy based on EUCAST V3.1.
Use for the EUCAST Blended panel class and NBC42, NBC49C and NM37 panels.
Do not report drug, therapy or MIC for P. aeruginosa.
Only systemic therapy will be reported.
Do not report therapy for Aeromonas spp, Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
NOTE: 1.
2.
3.
4.
5.
Moxifloxacin (Mxf)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
R
>
4
I
2
S
Therapy based on FDA approved breakpoints.
Do not report drug, therapy or MIC for P. aeruginosa.
Only systemic therapy will be reported.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
9020-7493B
Page 51 of 158
NOTE: 1.
2.
3.
4.
5.
6.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
I
8
S
4
S
Therapy based on SFM 2012.
Use for EUCAST panel class.
Only urine therapy will be reported.
For Dried Overnight panels, do not report drug, therapy or MIC for E. cloacae and K. pneumoniae.
Do not report therapy for Salmonella because the ability of the dried gram negative panels to detect
Nalidixic Acid resistance in Salmonella strains is unknown, resistant strains were not available at the
time of comparative testing. An alternate method should be used.
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
S
Therapy based on CLSI M100-S22.
Only urine therapy will be reported.
For Dried Overnight panels, do not report drug, therapy or MIC for E. cloacae and K. pneumoniae.
Do not report therapy for Y. pestis.
Do not report therapy for Salmonella because the ability of the dried gram negative panels to detect
Nalidixic Acid resistance in Salmonella strains is unknown, resistant strains were not available at the
time of comparative testing. An alternate method should be used.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, and Vibrio spp.
Netilmicin (Nt)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
I
I
I
8
S
S
S
4
S
S
S
2
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
3. Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides, S.
maltophilia, Vibrio spp. and Y. pestis.
Nitrofurantoin (Fd)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
64
S
32
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Only urine therapy will be reported.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
9020-7493B
Page 52 of 158
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
64
I
32
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only urine therapy will be reported.
3. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Norfloxacin (Nxn)
NOTE: 1.
2.
3.
4.
5.
6.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
1
I
S
S
0.5
S
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae and P aeruginosa therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Only urine therapy will be reported.
Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia, Vibrio spp. and Y. pestis.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and P. aeruginosa, all MICs of >1
will report as R, since these dilutions do not differentiate between S, I and R (S4, I=8, R16).
Norfloxacin (Nxn)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
1
I
0.5
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Only urine therapy will be reported.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Norfloxacin (Nxn)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
I
I
I
4
S
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only urine therapy will be reported.
3. Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia, Vibrio spp. and Y. pestis.
9020-7493B
Page 53 of 158
NOTE: 1.
2.
3.
4.
5.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
1
I
S
S
0.5
S
S
S
Enterobacteriaceae therapy based on EUCAST V3.1.
Non-Enterobacteriaceae and P aeruginosa therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia and Y. pestis.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae and P. aeruginosa , all MICs of
>1 will report as R, since these dilutions do not differentiate between S, I and R (S2, I=4, R8).
Ofloxacin (Ofl)
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
4
R
2
R
1
I
0.5
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class.
3. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Y. pestis.
Ofloxacin (Ofl)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
4
I
I
I
2
S
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia and Y. pestis.
Ofloxacin (Ofl)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
4
I
I
I
2
S
S
S
Therapy based on CLSI M100-S22.
For Rapid fluorogenic panel breakpoint format, do not report drug, therapy or MIC for A. baumannii, A.
haemolyticus, A. baumannii/haemolyticus, Acinetobacter spp. or P. aeruginosa. See back of therapy
guide for species names.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides, S.
maltophilia and Y. pestis.
For Dried Overnight panels, do not report therapy for Acinetobacter spp.
9020-7493B
Page 54 of 158
NOTE: 1.
2.
3.
4.
5.
6.
4.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
64
R
R
16
I
S
8
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report drug, therapy or MIC for C. koseri and S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp. and Plesiomonas shigelloides.
Piperacillin (Pi)
NOTE: 1.
2.
3.
NON-ENTEROBACTERIACEAE
>
R
N/R
R
16
I
S
S
8
S
S
S
4
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NBC45, NBC46, NM40 and NUC56 panels.
Do not report drug, therapy or MIC for C. koseri and S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, and Plesiomonas shigelloides.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >16 will report as N/R,
since these dilutions do not differentiate between I and R (S16, I=32-64, R128).
Piperacillin (Pi)
NOTE: 1.
2.
3.
4.
5.
ENTEROBACTERIACEAE
>
R
R
R
64
R
I
R
16
I
S
S
8
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E (use CLSI M100-S22
breakpoints), NM40 and NUC56 panels.
Do not report drug, therapy or MIC for C. koseri and S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, and Plesiomonas shigelloides.
Piperacillin (Pi)
NOTE: 1.
2.
3.
4.
5.
6.
7.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
128
R
R
R
64
I
I
I
32
I
I
I
16
S
S
S
8
S
S
S
Therapy based on CLSI M100-S22.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, and Plesiomonas
shigelloides.
Do not report drug, therapy or MIC for S. maltophilia.
9020-7493B
Page 55 of 158
NOTE: 1.
2.
3.
4.
4.
5.
6.
5.
6.
7.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
64
R
I
R
32
R
I
R
16
I
S
S
8
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E (use CLSI M100-S22
breakpoints), NM40 and NUC56 panels.
Do not report drug, therapy or MIC for S. maltophilia and Acinetobacter species. See back of therapy
guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and B. pseudomallei.
Piperacillin-Tazobactam
(P/T)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
R
64
I
I
S
16
S
S
S
Therapy based on CLSI M100-S21.
Use for RNBC3 and RNUC1 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides and S.
maltophilia.
Piperacillin-Tazobactam
(P/T)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
R
R
16
I
S
S
8
S
S
S
4
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S22.
Use for NBC45, NBC46, NM40 and NUC56 panels.
Do not report drug, therapy or MIC for S. maltophilia and Acinetobacter species. See back of therapy
guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and B. pseudomallei.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >16 will report as R,
since these dilutions do not differentiate between I and R (S16, I=32-64, R128).
Piperacillin-Tazobactam
(P/T)
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
64
R
R
16
I
S
8
S
S
4
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class.
3. Do not report drug, therapy or MIC for S. maltophilia and Acinetobacter species. See back of therapy
guide for species names.
4. Do not report therapy for Y. pestis because dangerously misleading results can occur.
9020-7493B
Page 56 of 158
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
I
32
I
I
I
16
S
S
S
8
S
S
S
Therapy based on CLSI M100-S22.
For Dried Overnight panels, do not report drug, therapy or MIC for S. maltophilia and Acinetobacter
species. See back of therapy guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and B. pseudomallei.
Tetracycline (Te)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
8
I
4
S
NOTE: 1. Therapy based on SFM 2012.
2. Use for EUCAST blended and EUCAST panel classes.
Tetracycline (Te)
P. AERUGINOSA
R
I
S
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
8
4
2
R
I
S
S
R
I
S
S
MIC
B. PSEUDOMALLEI
Y. PESTIS
P. AERUGINOSA
V. CHOLERAE
R
I
S
S
>
R
R
8
I
I
4
S
S
2
S
S
NOTE: 1. Enterobacteriaceae (except V. cholerae and Y. pestis) and Non-Enterobacteriaceae (except B.
pseudomallei) therapies based on CLSI M100-S22. V. cholerae, Y. pestis and B. pseudomallei
therapies based on CLSI M45-A2.
2. Do not report therapy for B. cepacia and S. maltophilia.
Ticarcillin (Ti)
NOTE: 1.
2.
3.
4.
5.
6.
7.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
PSEUDOMONAS SPP.
>
R
N/R
R
32
R
I
R
16
I
S
S
8
S
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Pseudomonas spp.) therapy based on CLSI M100-S21.
Use for EUCAST Blended panel class, except for NC71E (use CLSI M100-S21 breakpoints) panel.
Do not report drug, therapy or MIC for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides and
Vibrio spp.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >32 will report as N/R,
since these dilutions do not differentiate between I and R (S16, I=32-64, R128).
9020-7493B
Page 57 of 158
NOTE: 1.
2.
3.
4.
5.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
S
32
I
I
S
16
S
S
S
Therapy based on CLSI M100-S21.
For Dried Overnight panels, do not report drug, therapy or MIC for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides and
Vibrio spp.
Ticarcillin (Ti)
NOTE: 1.
2.
3.
4.
ACINETOBACTER SPP.
>
R
R
64
R
R
16
N/R
S
Therapy based on EUCAST V3.1.
Use for NC48 panel.
Do not report drug, therapy or MIC for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 16 will report as N/R,
since these dilutions do not differentiate between S and I (S8, I=16, R>16).
Ticarcillin (Ti)
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
>
R
R
64
R
R
32
R
R
16
I
S
8
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class, except for NC48 panel.
Do not report drug, therapy or MIC for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Ticarcillin (Ti)
NOTE: 1.
2.
3.
4.
5.
6.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
S
16
S
S
S
Therapy based on CLSI M100- S21.
Use for RNBC3 and RNUC1 panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides, S.
maltophilia and Vibrio spp.
9020-7493B
Page 58 of 158
NOTE: 1.
2.
3.
4.
5.
NON-ENTEROBACTERIACEAE
PSEUDOMONAS
SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
64
R
R
32
R
R
16
I
S
8
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class, except for NC48 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
NOTE: 1.
2.
3.
4.
5.
ENTEROBACTERIACEAE
>
R
R
16
I
S
8
S
S
Enterobacteriaceae and Pseudomonas spp. therapies based on EUCAST V3.1.
Use for EUCAST Blended panel class.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp, Plesiomonas shigelloides and Vibrio spp.
Do not report drug, therapy or MIC for Non-Enterobacteriacea (other than Pseudomonas species).
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
64
R
R
16
N/R
S
Therapy based on EUCAST V3.1.
Use for NC48 panel.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 16 will report as N/R,
since these dilutions do not differentiate between S and I (S8, I=16, R>16).
NOTE: 1.
2.
3.
4.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
64
I
I
32
I
I
16
S
S
8
S
S
Therapy based on CLSI M100-S22.
Do not report drug, MIC or therapy for P. aeruginosa.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides and Vibrio spp.
Page 59 of 158
NOTE: 1.
2.
3.
4.
5.
3.
4.
4.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
4
R
2
I
1
S
0.5
S
0.25
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended, EUCAST panel classes, and NBC42, NBC43, NBC49C, NC54, NC70C,
NC71C, NM44C panels.
Do not report drug, therapy or MIC for Acinetobacter spp., P. mirabilis, Non-Enterobacteriaceae and P.
aeruginosa.
Do not report therapy for Y. pestis.
Tigecycline (Tgc)
NOTE: 1.
2.
3.
ENTEROBACTERIACEAE
>
R
R
64
I
I
16
S
S
Therapy based on CLSI M100-S21.
Use for RNBC3 panel.
For Rapid fluorogenic panel breakpoint format, do not report drug, therapy or MIC for P. aeruginosa, E. coli or
Klebsiella spp. See back of therapy guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides, and Vibrio spp.
Tigecycline (Tgc)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
2
I
1
S
Enterobacteriaceae therapy based on ANVISA.
Use for NC66 panel.
Do not report drug, therapy or MIC for Acinetobacter spp., P. mirabilis, Non-Enterobacteriaceae and P.
aeruginosa.
Do not report therapy for Y. pestis.
Tigecycline (Tgc)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
4
I
2
S
1
S
NOTE: 1. Therapy based on FDA approved breakpoints.
2. Do not report drug, therapy or MIC for Acinetobacter spp., P. mirabilis, Non-Enterobacteriaceae and P.
aeruginosa.
3. Do not report therapy for Y. pestis.
9020-7493B
Page 60 of 158
NOTE: 1.
2.
3.
4.
5.
3.
4.
5.
6.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
R
R
8
R
I
R
R
4
I
S
S
S
2
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Acinetobacter spp. and Pseudomonas spp.) therapy based on CLSI
M100-S22.
Use for EUCAST Blended panel class, except for NBC45, NBC46, NBC49E (use CLSI M100-S22
breakpoints), NM40 and NUC56 panels.
Do not report therapy for Salmonella/Shigella group because dangerously misleading results can
occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides, S.
maltophilia, Vibrio spp. and Y. pestis.
Tobramycin (To)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS
SPP.
>
R
R
R
R
4
I
S
S
S
2
S
S
S
S
Enterobacteriaceae, Acinetobacter spp. and Pseudomonas spp. therapies based on EUCAST V3.1.
Non-Enterobacteriaceae (except Acinetobacter spp. and Pseudomonas spp.) therapies based on CLSI
M100-S22.
Use for NBC45, NBC46, NM40 and NUC56 panels.
Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides, S.
maltophilia, Vibrio spp. and Y. pestis.
Based on CLSI interpretive guidelines for Non-Enterobacteriaceae, all MICs of >4 will report as R, since
these dilutions do not differentiate between I and R (S4, I=8, R16).
Tobramycin (To)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
R
8
R
R
R
4
I
S
S
2
S
S
S
1
S
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Tobramycin (To)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
R
R
R
8
I
I
I
4
S
S
S
2
S
S
S
1
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
3. Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides,
S. maltophilia, Vibrio spp. and Y. pestis.
9020-7493B
Page 61 of 158
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
8
S
Therapy based on CLSI M100-S22.
Only urine therapy will be reported.
For Rapid fluorogenic panel breakpoint format, do not report drug, therapy or MIC for A. baumannii, A.
haemolyticus, A. baumannii/haemolyticus and Acinetobacter spp. See back of therapy guide for
species names.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
TrimethoprimSulfamethoxazole
(T/S)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
>
R
I
S
R
R
S
R
I
S
4/76
2/38
MIC
B. PSEUDOMALLEI
V. CHOLERAE
S. MALTOPHILIA
P. AERUGINOSA
Y. PESTIS
>
R
R
R
R
R
R
S
R
S
S
S
S
Enterobacteriaceae (except Y. pestis), Acinetobacter spp. and S. maltophilia therapies based on
EUCAST.
Non-Enterobacteriaceae (including Pseudomonas spp. other than P. aeruginosa) therapy based on
CLSI M100-S22 and B. pseudomallei, V. cholerae, and Y. pestis therapies based on CLSI M45-A2.
Use for EUCAST blended panel class, except for NC53 and NC58 panels.
Do not report therapy for P. aeruginosa.
4/76
2/38
NOTE: 1.
2.
3.
4.
TrimethoprimSulfamethoxazole
(T/S)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
ACINETOBACTER
SPP.
2/38
>
R
S
R
S
R
S
MIC
B. PSEUDOMALLEI
V. CHOLERAE
Y. PESTIS
P. AERUGINOSA S. MALTOPHILIA
R
S
>
NOTE: 1.
2.
3.
4.
5.
R
R
R
2/38
S
S
S
Enterobacteriaceae (except Y. pestis), Acinetobacter spp. and S. maltophilia therapies based on
EUCAST V3.1.
Non-Enterobacteriaceae (including Pseudomonas spp. other than P. aeruginosa) therapy based on
CLSI M100-S22 and B. pseudomallei, V. cholerae, and Y. pestis therapy based on CLSI M45-A2.
Use for NC53 and NC58 panels.
Do not report therapy for P. aeruginosa.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, Acinetobacter spp., and S. maltophilia
all MICs of >2/38 will report as R, since these dilutions do not differentiate between I and R with
Enterobacteriaceae and Acinetobacter spp. (S2/38, I=4/76, R>4/76), and S and R with S. maltophilia
(S4/76, R>4/76).
9020-7493B
Page 62 of 158
MIC
TrimethoprimSulfamethoxazole (T/S)
MIC
ENTEROBACTERIACEAE
>
R
4/76
I
2/38
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for NM39 and NUC57panels.
3. Do not report therapy for P. aeruginosa.
NOTE: 1.
2.
3.
4.
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
R
I
S
R
S
S
ACINETOBACTER SPP.
>
R
R
R
8/152
R
R
R
2/38
S
S
S
Therapies for y based on EUCAST V3.1.
Use for NC48 panel.
Do not report therapy for P. aeruginosa.
Based on EUCAST interpretive guidelines for Enterobacteriaceae and Acinetobacter spp., all MICs of
> 2/38 will report as R, since these dilutions do not differentiate between I and R (S2/38, I=4/76,
R>4/76).
TrimethoprimSulfamethoxazole (T/S)
MIC
ENTEROBACTERIACEAE
4/76
2/38
1/19
0.5/9.5
>
R
R
S
S
S
MIC
B. PSEUDOMALLEI
NON-ENTEROBACTERIACEAE P. AERUGINOSA
V. CHOLERAE
R
R
S
S
S
R
R
S
S
S
Y. PESTIS
>
R
R
4/76
R
R
2/38
S
S
1/19
S
S
0.5/9.5
S
S
NOTE: 1. Enterobacteriaceae (except V. cholerae and Y. pestis) and Non-Enteroacteriaceae (except B.
pseudomallei) therapies based on CLSI M100-S22. B. pseudomallei, V. cholerae, and Y. pestis
therapies based on CLSI M45-A2.
2. Do not report therapy for P. aeruginosa.
TrimethoprimSulfamethoxazole (T/S)
MIC
ENTEROBACTERIACEAE
2/38
0.5/9.5
>
R
S
S
MIC
B. PSEUDOMALLEI
NON-ENTEROBACTERIACEAE P. AERUGINOSA
V. CHOLERAE
R
S
S
R
S
S
Y. PESTIS
>
R
R
2/38
S
S
0.5/9.5
S
S
NOTE: 1. Enterobacteriaceae (except V. cholerae and Y. pestis) and Non-Enteroacteriaceae (except B.
pseudomallei) therapies based on CLSI M100-S22. B. pseudomallei, V. cholerae and Y. pestis
therapies based on CLSI M45-A2.
2. Use for RNBC3 and RNUC1 panels.
3. Do not report drug, therapy or MIC for P. aeruginosa.
9020-7493B
Page 63 of 158
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
32
R
16
I
8
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended panel class.
Do not report drug, therapy or MIC for beta-hemolytic streptococci (S. agalactiae).
Do not report therapy for enterococci because dangerously misleading results can occur.
Amikacin (Ak)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
32
I
16
S
8
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for beta-hemolytic streptococci (S. agalactiae).
3. Do not report therapy for enterococci because dangerously misleading results can occur.
AmoxicillinK Clavulanate (Aug)
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8/4
R
4/2
S
2/1
S
1/0.5
S
0.5/0.25
S
Enterococci and streptococci therapy based on EUCAST V3.1, see notes 7 and 8.
Staphylococci therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class.
For S. aureus and S. lugdunensis, if Oxacillin is >2 or Cefoxitin Screen (CfxS) is >4, report Amoxicillin-K
Clavulanate as resistant regardless of MIC.
For panels containing only Oxacillin with coagulase-negative staphylococci (CNS) other than S.
lugdunensis, if Oxacillin MIC is 0.5, report Amoxicillin-K Clavulanate as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Amoxicillin-K Clavulanate as
resistant regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of
the guide.
Do not report therapy for enterococci, refer to Ampicillin result.
For streptococci, refer to Penicillin result.
9020-7493B
Page 64 of 158
NOTE: 1.
2.
3.
4.
5.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
16/8
R
8/4
R
4/2
S
2/1
S
Therapy based on CLSI M100-S22.
For S. aureus and S. lugdunensis, if Oxacillin is >2 or Cefoxitin Screen (CfxS) is >4, report Amoxicillin-K
Clavulanate as resistant regardless of MIC.
For panels containing only Oxacillin with coagulase-negative staphylococci (CNS) other than S.
lugdunensis, if Oxacillin MIC is 0.5, report Amoxicillin-K Clavulanate as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Amoxicillin-K Clavulanate as
resistant regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of
the guide.
For streptococci and beta-lactamase negative enterococci, refer to Penicillin result.
Ampicillin
(Am)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
8
R
I
R
4
R
S
I
0.25
S
S
S
S
S
NOTE: 1. Enterococci therapy based on EUCAST V3.1.
2. Staphylococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100S22. L. monocytogenes therapies based on CLSI M45-A2.
3. Use for PC42E and PM33E panels.
4. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
5. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
6. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
7. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
8. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
9. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >0.25.
10. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations
will be provided if the result is >0.25.
9020-7493B
Page 65 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
R
8
R
I
N/R
R
4
R
S
N/R
I
2
R
S
N/R
I
S
1
R
S
N/R
I
S
0.5
N/R
S
N/R
N/R
S
NOTE: 1. Enterococci therapy based on EUCAST V3.1.
2. Staphylococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100S22. L. monocytogenes therapies based on CLSI M45-A2.
3. Use for PM32 panel.
4. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
5. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
6. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
7. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
8. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
9. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 0.5 will report as N/R, since these dilutions do not differentiate between S and
NS.
10. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations
will be provided if the result is >2.
11. Based on CLSI interpretive guidelines for staphylococci, all MICs of 0.5 will report as N/R, since
these dilutions do not differentiate between S and R (S0.25, R0.5).
12. Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 0.5 will report as N/R, since
these dilutions do not differentiate between S and I (S0.25, I=0.5-4, R8).
9020-7493B
Page 66 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
R
8
R
I
N/R
R
4
R
S
N/R
I
2
R
S
N/R
I
S
1
N/R
S
N/R
N/R
S
NOTE: 1. Enterococci therapy based on EUCAST V3.1.
2. Staphylococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100S22. L. monocytogenes therapies based on CLSI M45-A2.
3. Use for PC35 and PC38 panels.
4. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
5. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
6. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
7. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
8. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
9. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 1 will report as N/R, since these dilutions do not differentiate between S and
NS.
10. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >2.
11. Based on CLSI interpretive guidelines for staphylococci, all MICs of 1 will report as N/R, since these
dilutions do not differentiate between S and R (S0.25, R0.5).
12. Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 1 will report as N/R, since
these dilutions do not differentiate between S and I (S0.25, I=0.5-4, R8).
9020-7493B
Page 67 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
R
8
R
I
N/R
R
4
R
S
N/R
I
2
N/R
S
N/R
N/R
S
NOTE: 1. Enterococci therapy based on EUCAST V3.1.
2. Staphylococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100S22. L. monocytogenes therapies based on CLSI M45-A2.
3. Use for PBC33 panel.
4. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
5. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
6. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
7. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
8. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
9. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 2 will report as N/R, since these dilutions do not differentiate between S and
NS.
10. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations
will be provided if the result is >2.
11. Based on CLSI interpretive guidelines for staphylococci, all MICs of 2 will report as N/R, since these
dilutions do not differentiate between S and R (S0.25, R0.5).
12. Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 2 will report as N/R, since
these dilutions do not differentiate between S and I (S0.25, I=0.5-4, R8).
9020-7493B
Page 68 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
R
N/R
8
R
I
N/R
R
N/R
4
N/R
S
N/R
N/R
N/R
NOTE: 1. Enterococci therapy based on EUCAST V3.1.
2. Staphylococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100S22. L. monocytogenes therapies based on CLSI M45-A2.
3. Use for PBC32 panel.
4. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
5. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
6. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
7. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
8. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant regardless of
MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
9. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 4 will report as N/R, since these dilutions do not differentiate between S and
NS.
10. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, all MICs of 4
will report as N/R, since these dilutions do not differentiate between S and NS.
11. Based on CLSI interpretive guidelines for staphylococci, all MICs of 4 will report as N/R, since these
dilutions do not differentiate between S and R (S0.25, R0.5).
12. Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 4 will report as N/R, since
these dilutions do not differentiate between S and I (S0.25, I=0.5-4, R8).
Ampicillin
(Am)
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
8
I
4
S
2
S
1
S
0.5
S
0.25
S
0.12
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report therapy for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci (including viridans streptococci (S. bovis group))
except for beta-hemolytic streptococci (S. agalactiae).
For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
For staphylococci, refer to the Cefoxitin Screen and/or Oxacillin result.
9020-7493B
Page 69 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
MIC
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
8
R
S
R
4
R
S
I
2
R
S
I
S
1
R
S
I
S
0.5
R
S
I
S
0.25
S
S
S
S
S
Staphylococci, Enterococci beta-hemolytic streptococci and viridans streptococci therapies based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
Do not report drug, therapy or MIC for all streptococci, except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
For streptococci refer to Penicillin result.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant regardless of
MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
If beta-lactamase positive for staphylococci or enterococci, report Ampicillin as Blac regardless of MIC.
For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci, no
interpretations will be provided if the result is >0.25.
The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations
will be provided if the result is >2.
Ampicillin
(Am)
NOTE: 1.
STAPHYLOCOCCI
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
N/R
8
R
S
N/R
0.25
S
S
S
S
S
Staphylococci, Enterococci beta-hemolytic streptococci and viridans streptococci therapies based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
Do not report drug, therapy or MIC for all streptococci, except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
For streptococci refer to Penicillin result.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant regardless of
MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
If beta-lactamase positive for staphylococci or enterococci, report Ampicillin as Blac regardless of MIC.
For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci, no
interpretations will be provided if the result is >0.25
The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations
will be provided if the result is >0.25.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >0.25 will report as N/R,
since these dilutions do not differentiate between I and R (S0.25, I=0.5-4, R8).
9020-7493B
Page 70 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
R
8
R
S
N/R
R
4
R
S
N/R
I
2
N/R
S
N/R
N/R
S
NOTE: 1. Staphylococci, Enterococci beta-hemolytic streptococci and viridans streptococci therapies based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2.
2. Use for PC29, PC33, PC34, PC40, PC41, PM26 and PM29 panels.
3. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
4. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
5. Do not report drug, therapy or MIC for all streptococci, except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
6. For streptococci refer to Penicillin result.
7. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
8. If beta-lactamase positive for staphylococci or enterococci, report Ampicillin as Blac regardless of MIC.
9. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
10. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 2 will report as N/R, since these dilutions do not differentiate between S and
NS.
11. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >2.
12. Based on CLSI interpretive guidelines for staphylococci, all MICs of 2 will report as N/R, since these
dilutions do not differentiate between S and R (S 0.25, R0.5).
13. Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 2, will report as N/R, since
these dilutions do not differentiate between S and I (S0.25, I=0.5-4, R8).
9020-7493B
Page 71 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
R
8
R
S
N/R
R
4
R
S
N/R
I
2
R
S
N/R
I
S
1
N/R
S
N/R
N/R
S
NOTE: 1. Staphylococci, Enterococci beta-hemolytic streptococci and viridans streptococci therapies based on
CLSI M100-S22. L. monocytogenes therapy based on CLSI M45-A2.
2. Use for PC32 panel.
3. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Ampicillin as
resistant regardless of MIC.
4. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin as resistant regardless of MIC.
5. Do not report drug, therapy or MIC for all streptococci, except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
6. For streptococci refer to Penicillin result.
7. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
8. If beta-lactamase positive for staphylococci or enterococci, report Ampicillin as Blac regardless of MIC.
9. For staphylococci, if Penicillin MIC is >0.12, report Ampicillin as resistant regardless of MIC.
10. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 1 will report as N/R, since these dilutions do not differentiate between S and
NS.
11. The CLSI interpretative guideline for Ampicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >2.
12. Based on CLSI interpretive guidelines for staphylococci, all MICs of 1, will report as N/R, since these
dilutions do not differentiate between S and R (S 0.25, R0.5).
13. Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 1, will report as N/R, since
these dilutions do not differentiate between S and I (S0.25, I=0.5-4, R8).
Amp-Sulbactam (A/S)
NOTE: 1.
2.
3.
4.
5.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
16/8
I
8/4
S
Therapy based on CLSI M100-S22.
For S. aureus and S. lugdunensis, if oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Ampicillin-Sulbactam as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ampicillin-Sulbactam as resistant
regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ampicillin-Sulbactam as
resistant regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of
the guide.
For streptococci and beta-lactamase negative enterococci, refer to Penicillin result.
9020-7493B
Page 72 of 158
MIC
STAPHYLOCOCCI
(S. aureus)
ENTEROCOCCI
STREPTOCOCCI
L. monocytogenes
>
R
8
I
4
S
NOTE: 1. Therapy based on guidelines other than CLSI and EUCAST.
2. Do not report drug, therapy or MIC for enterococci, streptococci and L. monocytogenes.
Azithromycin (Azi)
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
L. monocytogenes
>
R
2
I
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended panel class.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for enterococci, streptococci or L. monocytogenes.
Azithromycin (Azi)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
L. monocytogenes
>
R
4
I
2
S
1
S
0.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
3. Do not report drug, therapy or MIC for enterococci, streptococci or L. monocytogenes.
Cefazolin (Cfz)
NOTE: 1.
2.
3.
4.
5.
6.
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
L. monocytogenes
>
R
16
I
8
S
4
S
2
S
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Cefazolin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin is 0.5, report Cefazolin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefazolin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
For streptococci, refer to Penicillin result.
Page 73 of 158
3.
4.
5.
Cefepime (Cpe)
3.
4.
5.
6.
7.
8.
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
L. monocytogenes
>
R
2
I
1
S
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Cefdinir as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefdinir as resistant regardless of
MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefdinir as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
NOTE: 1.
2.
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
N/R
R
16
I
N/R
R
8
S
N/R
R
4
S
N/R
N/R
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Cefepime
as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefepime as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefepime as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
For streptococci, refer to Penicillin result.
The CLSI interpretative guideline for Cefepime with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 4 will report as N/R, since these dilutions do not differentiate between S and
NS.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs 4 will report as N/R, since these
dilutions do not differentiate between S, I and R (S 1, I=2, R4).
9020-7493B
Page 74 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
5.
6.
7.
8.
9.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
N/R
N/R
R
8
S
N/R
R
4
S
N/R
N/R
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Cefepime
as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefepime as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefepime as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
For streptococci, refer to Penicillin result.
Based on CLSI interpretive guidelines for staphylococci, all MICs >8 will report as N/R, since these dilutions
do not differentiate between I and R (S 8, I=16, R32).
The CLSI interpretative guideline for Cefepime with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 4 will report as N/R, since these dilutions do not differentiate between S and
NS.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs 4 will report as N/R, since these
dilutions do not differentiate between S, I and R (S 1, I=2, R4).
Cefotaxime (Cft)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
N/R
N/R
R
2
S
N/R
I
1
S
N/R
S
Enterococci therapy based on EUCAST V3.1.
Staphylococci and beta-hemolytic and viridans streptococci therapies based on CLSI M100-S22.
Use for PM32 panel.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Cefotaxime as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefotaxime as resistant
regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefotaxime as resistant regardless of
MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
Based on CLSI interpretive guidelines for staphylococci, all MICs of >2 will report as N/R, since these
dilutions do not differentiate between S, I and R (S 8, I=16-32, R 64).
The CLSI interpretative guideline for Cefotaxime with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 1 will report as N/R, since these dilutions do not differentiate between S and
NS.
9020-7493B
Page 75 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
3.
4.
5.
6.
7.
8.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
16
0.5
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For staphylococci, refer to Cefoxitin Screen and/or Oxacillin result.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Cefotaxime as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefotaxime as resistant
regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefotaxime as resistant regardless of
MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
Do not report drug, therapy or MIC for all streptococci (including viridans streptococci (S. bovis group))
except for beta-hemolytic streptococci (S. agalactiae).
For beta-hemolytic streptococci (S. agalactiae), refer to Penicillin result.
Cefotaxime (Cft)
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
N/R
32
I
N/R
16
I
N/R
8
S
N/R
1
S
S
0.5
S
S
S
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results can
occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Cefotaxime as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefotaxime as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than
S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefotaxime as resistant regardless of MIC. For
additional information refer to Cefoxitin Screen section in the front of therapy guide.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S. agalactiae)
and viridans streptococci (S. bovis group).
The CLSI interpretative guideline for Cefotaxime with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci, no
interpretations will be provided if the result is >0.5.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >1 will report as N/R, since these
dilutions do not differentiate between S, I and R (S 1, I=2, R 4).
9020-7493B
Page 76 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
N/R
R
32
I
N/R
R
8
S
N/R
N/R
Therapy based on CLSI M100-S22.
Use for panels with breakpoint format.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results can
occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Cefotaxime
as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefotaxime as resistant regardless of
MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefotaxime as resistant regardless of
MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
For streptococci, refer to Penicillin result.
The CLSI interpretative guideline for Cefotaxime with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 8 will report as N/R, since these dilutions do not differentiate between S and
NS.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of 8 will report as N/R, since
these dilutions do not differentiate between S, I and R (S 1, I=2, R 4).
Ceftaroline (Cpt)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
(S. aureus)
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
1
S
0.5
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Do not report drug, MIC or therapy for enterococci, L. monocytogenes and streptococci.
Do not report therapy for coagulase negative staphylococci.
9020-7493B
Page 77 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
3.
4.
5.
6.
7.
8.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
N/R
R
32
I
N/R
R
16
I
N/R
R
8
S
N/R
R
4
S
N/R
N/R
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Ceftriaxone as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ceftriaxone as resistant regardless of
MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than
S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ceftriaxone as resistant regardless of MIC.
For additional information refer to Cefoxitin Screen section in the front of the guide.
For streptococci, refer to Penicillin result.
The CLSI interpretative guideline for Ceftriaxone with beta-hemolytic streptococci is 0.5 for
susceptible. Because intermediate and resistant interpretations have not been defined for betahemolytic streptococci, all MICs of 4 will report as N/R, since these dilutions do not differentiate
between S and NS.
Based on CLSI interpretive guidelines for viridans streptococci, MICs of 4 will report as N/R, since these
dilutions do not differentiate between I and R (S 1, I =2, R4).
Ceftriaxone (Cax)
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
N/R
R
32
I
N/R
R
16
I
N/R
R
8
S
N/R
N/R
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Ceftriaxone as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ceftriaxone as resistant regardless of
MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than
S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ceftriaxone as resistant regardless of MIC. For
additional information refer to Cefoxitin Screen section in the front of the guide.
For streptococci, refer to Penicillin result.
The CLSI interpretative guideline for Ceftriaxone with beta-hemolytic streptococci is 0.5 for
susceptible. Because intermediate and resistant interpretations have not been defined for betahemolytic streptococci, all MICs of 8 will report as N/R, since these dilutions do not differentiate
between S and NS.
Based on CLSI interpretive guidelines for viridans streptococci, MICs of 8 will report as N/R, since these
dilutions do not differentiate between I and R (S 1, I =2, R4).
9020-7493B
Page 78 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
4.
5.
6.
7.
8.
9.
3.
4.
5.
6.
ENTEROCOCCI
STREPTOCOCCI
L. monocytogenes
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
N/R
8
S
4
S
Therapy based on CLSI M100-S22.
Use for PM32 panel.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Cefuroxime sodium as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefuroxime sodium as resistant
regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than
S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefuroxime sodium as resistant regardless of MIC.
For additional information refer to Cefoxitin Screen section in the front of the guide.
The CLSI breakpoints for Cefuroxime axetil (oral) are S4, I=8-16, R32.
For streptococci, refer to Penicillin result.
Based on CLSI interpretive guidelines for staphylococci, all MICs of >8 will report as N/R, since these
dilutions do not differentiate between I and R (S 8, I =16, R32).
Cephalothin (Cf)
NOTE: 1.
2.
STAPHYLOCOCCI
>
R
16
I
8
S
4
S
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results
can occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Cefuroxime sodium as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cefuroxime sodium as resistant
regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cefuroxime sodium as
resistant regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of
the guide.
The CLSI breakpoints for Cefuroxime axetil (oral) are S4, I=8-16, R32.
For streptococci, refer to Penicillin result.
NOTE: 1.
2.
3.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
16
I
8
S
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results can
occur.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Cephalothin as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Cephalothin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than
S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Cephalothin as resistant regardless of MIC. For
additional information refer to Cefoxitin Screen section in the front of the therapy guide.
For streptococci, refer to Penicillin result.
9020-7493B
Page 79 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
16
I
I
R
8
S
S
I
4
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S. agalactiae)
and viridans streptococci (S. bovis group).
ChIoramphenicol (C)
NOTE: 1.
2.
3.
4.
5.
6.
7.
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
16
I
I
R
8
S
S
N/R
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S. agalactiae)
and viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for streptococci, all MICs of 8 will report as N/R, since these
dilutions do not differentiate between S and I (S4, I=8, R16).
Chloramphenicol (C)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
N/R
R
8
S
N/R
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Use for PBC33 and PM32 panels.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S. agalactiae)
and viridans streptococci (S. bovis group).
Do not report drug, therapy or MIC for staphylococci.
Based on CLSI interpretive guidelines for enterococci, all MICs of >8 will report as N/R, since these
dilutions do not differentiate between I and R (S8, I=16, R32).
Based on CLSI interpretive guidelines for streptococci, all MICs of 8 will report as N/R, since these
dilutions do not differentiate between S and I (S4, I=8, R16).
Ciprofloxacin (Cp)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
2
R
I
1
S
S
0.5
S
S
NOTE: 1. Staphylococci therapy based on EUCAST V3.1.
2. Enterococci therapy based on CLSI M100-S22.
3. Use for EUCAST Blended panel class, except for PBC33 and PM32 panels.
9020-7493B
Page 80 of 158
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
STREPTOCOCCI
>
R
R
1
S
S
0.5
S
S
Staphylococci therapy based on EUCAST V3.1.
Enterococci therapy based on CLSI M100-S22.
Use for PBC33 and PM32 panels.
Based on CLSI interpretive guidelines for enterococci, all MICs of >1 will report as R, since these
dilutions do not differentiate between I and R (S1, I=2, R4).
Ciprofloxacin (Cp)
MIC
STAPHYLOCOCCI
>
R
2
I
1
S
0.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
Clarithromycin (Cla)
NOTE: 1.
2.
3.
4.
ENTEROCOCCI
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
I
S
S
ENTEROCOCCI
STREPTOCOCCI
>
R
2
I
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended panel class.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for enterococci, L. monocytogenes or streptococci.
Clarithromycin (Cla)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
4
I
2
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
3. Do not report drug, therapy or MIC for enterococci, streptococci or L. monocytogenes.
Clindamycin (Cd)
NOTE: 1.
2.
3.
4.
5.
6.
7.
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
2
R
R
1
R
R
0.5
I
I
0.25
S
S
Staphylococci therapy based on EUCAST V3.1.
Streptococci therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Only systemic therapy will be reported.
Do not report therapy for enterococci because dangerously misleading results can occur.
Do not report drug, therapy or MIC for all streptococci, except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
For staphylococci, if Inducible Clindamycin (ICd) test is positive (>4/0.5) report Clindamycin as
resistant regardless of MIC.
Page 81 of 158
NOTE: 1.
2.
3.
4.
5.
6.
5.
5.
ENTEROCOCCI
STREPTOCOCCI
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
4
R
R
2
I
R
1
I
R
0.5
S
I
0.25
S
S
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Do not report therapy for enterococci because dangerously misleading results can occur.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
For staphylococci, if Inducible Clindamycin (ICd) test is positive (>4/0.5) report Clindamycin as
resistant regardless of MIC.
Clindamycin (Cd)
NOTE: 1.
2.
3.
4.
STAPHYLOCOCCI
>
R
2
R
1
R
0.5
I
0.25
S
Therapy based on EUCAST V3.1.
Use for EUCAST panel class.
Only systemic therapy will be reported.
Do not report therapy for enterococci because dangerously misleading results can occur.
Do not report drug, therapy or MIC for all streptococci, including beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
For staphylococci, if Inducible Clindamycin (ICd) test is positive (>4/0.5) report Clindamycin as
resistant regardless of MIC.
Clindamycin (Cd)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
4
R
R
2
I
R
1
I
R
0.5
S
N/R
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Do not report therapy for enterococci because dangerously misleading results can occur.
For staphylococci, if Inducible Clindamycin (ICd) test is positive (>4/0.5) report Clindamycin as
resistant regardless of MIC.
Based on CLSI interpretive guidelines for streptococci, all MICs of 0.5 will report as N/R, since these
dilutions do not differentiate between S and I (S0.25, I=0.5, R1).
9020-7493B
Page 82 of 158
NOTE: 1.
2.
3.
4.
5.
6.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
4
R
S
R
2
R
S
R
1
S
S
S
S
0.5
S
S
S
S
0.25
S
S
S
S
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci and viridans streptococci therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and S. bovis group (Group D).
The CLSI interpretative guideline for Daptomycin with enterococci is 4 for susceptible. Because intermediate
and resistant interpretations have not been defined for enterococci, no interpretations will be provided if the
result is >4.
The CLSI interpretative guideline for Daptomycin with viridans streptococci is 1 for susceptible. Because
intermediate and resistant interpretations have not been defined for viridans streptococci, no interpretations will
be provided if the result is >1.
Daptomycin (Dap)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
4
R
R
2
R
R
1
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Daptomycin (Dap)
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
4
S
2
S
1
S
S
S
0.5
S
S
S
0.25
S
S
S
Therapy based on CLSI M100-S22.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
The CLSI interpretative guideline for Daptomycin with staphylococci and streptococci is 1 for
susceptible. Because intermediate and resistant interpretations have not been defined for
staphylococci and streptococci, no interpretations will be provided if the result is >1.
The CLSI interpretative guideline for Daptomycin with enterococci is 4 for susceptible. Because
intermediate and resistant interpretations have not been defined for enterococci, no interpretations will
be provided if the result is >4.
9020-7493B
Page 83 of 158
5.
6.
7.
8.
9.
Ertapenem (Etp)
3.
4.
5.
6.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
1
S
S
0.5
S
S
Enterococci therapy based on EUCAST V3.1.
Staphylococci and beta-hemolytic streptococci therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Do not report drug, therapy or MIC for Listeria monocytogenes and all Coagulase-Negative
Staphylococci (CNS) with MIC >0.5 for Ox or CfxS >4, including S. lugdunensis with an MIC >2 for
Oxacillin.
For S. aureus, if Oxacillin MIC is >2 and\or CfxS is >4, report Ertapenem as resistant regardless of
MIC.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
The CLSI interpretative guideline for Ertapenem with beta-hemolytic streptococci is 1 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >1.
Based on CLSI interpretive guidelines for staphylococci, all MICs of >1 will report as R, since these
dilutions do not differentiate between S, I and R (S2, I=4, R8).
NOTE: 1.
2.
3.
4.
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
4
I
2
S
1
S
S
0.5
S
S
Therapy based on CLSI M100-S22.
Do not report drug, therapy or MIC for Listeria monocytogenes and all Coagulase-Negative
Staphylococci (CNS) with MIC >0.5 for Ox or CfxS >4, including S. lugdunensis with an MIC >2 for
Oxacillin.
For S. aureus, if Oxacillin MIC is >2 and\or CfxS is >4, report Ertapenem as resistant regardless of MIC.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
The CLSI interpretative guideline for Ertapenem with beta-hemolytic streptococci is 1 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >1.
9020-7493B
Page 84 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
4.
5.
6.
7.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
N/R
4
I
N/R
2
S
N/R
Therapy based on CLSI M100-S22.
Do not report drug, therapy or MIC for Listeria monocytogenes and all Coagulase-Negative
Staphylococci (CNS) with MIC >0.5 for Ox or CfxS >4, including S. lugdunensis with an MIC >2 for
Oxacillin.
For S. aureus, if Oxacillin MIC is >2 and\or CfxS is >4, report Ertapenem as resistant regardless of MIC.
For streptococci, refer to Penicillin result.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
The CLSI interpretative guideline for Ertapenem with beta-hemolytic streptococci is 1 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, all MICs of 2will report as N/R, since these dilutions do not differentiate between S and
NS.
Erythromycin (E)
NOTE: 1.
2.
3.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
4
R
I
R
2
I
I
R
1
S
I
R
0.5
S
S
I
0.25
S
S
S
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for PBC32, PBC33, PC35, PC37, PC42E, PM32 and
PM33E panels.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Erythromycin (E)
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
4
R
I
R
2
I
I
R
1
S
I
R
0.5
S
S
N/R
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci therapy based on CLSI M100-S22.
Use for PC37, PC42E and PM33E panels.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Based on EUCAST interpretive guidelines for beta-hemolytic streptococci, all MICs of 0.5 will report
as N/R, since these dilutions do not differentiate between S and I (S0.25, I=0.5, R>0.5).
Page 85 of 158
7.
8.
9.
Erythromycin (E)
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
2
I
I
R
1
S
N/R
N/R
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci therapy based on CLSI M100-S22
Use for PBC32, PBC33 and PM32 panels.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for enterococci, all MICs of 1 will report as N/R, since these
dilutions do not differentiate between S, I and R (S0.5, I=1-4, R8).
Based on EUCAST interpretive guidelines for beta-hemolytic streptococci, all MICs of 1 will report as
N/R, since these dilutions do not differentiate between S, I and R (S0.25, I=0.5, R>0.5).
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
Erythromycin (E)
6.
STAPHYLOCOCCI
>
R
R
R
2
I
I
R
1
S
I
R
0.5
S
S
N/R
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci therapy based on CLSI M100-S22.
Use for PC35 panel.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for enterococci, all MICs of >2 will report as R, since these
dilutions do not differentiate between I and R (S0.5, I=1-4, R8).
Based on EUCAST interpretive guidelines for beta-hemolytic streptococci, all MICs of 0.5 will report
as N/R, since these dilutions do not differentiate between S and I (S0.25, I=0.5, R>0.5).
NOTE: 1.
2.
3.
4.
5.
6.
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
4
R
R
2
I
R
1
S
R
0.5
S
I
0.25
S
S
Therapy based on EUCAST V3.1.
Use for PC36 and PM31 panels.
Only systemic therapy will be reported
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
9020-7493B
Page 86 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
6.
4.
5.
6.
7.
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
4
I
I
R
2
I
I
R
1
I
I
R
0.5
S
S
I
0.25
S
S
S
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Use for PBC27, PC32, PM21, PM26 and PM29 panels.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Erythromycin (E)
NOTE: 1.
2.
3.
STAPHYLOCOCCI
>
R
R
8
R
R
4
R
R
2
I
R
1
S
N/R
Therapy based on EUCAST V3.1.
Use for PC30 panel.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Based on EUCAST interpretive guidelines for beta-hemolytic streptococci, all MICs of 1 will report as
N/R, since these dilutions do not differentiate between S and I (S0.25, I=0.5, R>0.5).
Erythromycin (E)
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
R
4
I
I
R
2
I
I
R
1
I
I
R
0.5
S
S
N/R
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Use for PBC28, PC20, PC21, PC29, PC31, PC33, PC34, PC39, PC40, PC41, PC42C, PM28 and
PM33C panels.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for beta-hemolytic streptococci, all MICs of 0.5 will report as
N/R, since these dilutions do not differentiate between S and I (S0.25, I=0.5, R1).
9020-7493B
Page 87 of 158
NOTE: 1.
2.
3.
4.
5.
6.
6.
7.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
4
I
I
R
0.5
S
S
I
0.25
S
S
S
Therapy based on CLSI M100-S22
Only systemic therapy will be reported.
Use for PC1A panel.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Erythromycin (E)
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
R
4
I
I
R
0.5
S
S
N/R
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Use for PBC20, PBC23 and PBC29 panels.
Do not report drug, therapy or MIC for L. monocytogenes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for beta-hemolytic streptococci, all MICs of 0.5 will report as
N/R, since these dilutions do not differentiate between S and I (S0.25, I=0.5, R1).
Fosfomycin (Fos)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
64
R
32
S
NOTE: 1. Therapy based on EUCAST V3.1.
Fusidic Acid (FA)
MIC
STAPHYLOCOCCI
>
16
2
NOTE: 1. Therapy based on SFM 2008.
Fusidic Acid (FA)
MIC
ENTEROCOCCI
STREPTOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
I
S
STAPHYLOCOCCI
N/R
>
2
S
NOTE: 1. Therapy based on SFM 2008.
2. Use for PBC33, PM31, PM32, PM33C and PM33E panel.
3. Based on SFM 2008 interpretive guidelines for staphylococci, all MICs of >2 will report as N/R, since
these dilutions do not differentiate between S, I and R (S2, I=4-16, R>16).
9020-7493B
Page 88 of 158
MIC
Gentamicin (Gm)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
>
4
I
2
S
1
S
0.5
S
NOTE: 1. Therapy based on FDA approved breakpoints.
NOTE: 1.
2.
3.
4.
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
R
4
R
2
R
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Do not report therapy for enterococci because dangerously misleading results can occur.
Do not report drug, therapy or MIC for all streptococci
Gentamicin (Gm)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
I
4
S
2
S
1
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for enterococci because dangerously misleading results can occur.
3. Do not report drug, therapy or MIC for for all streptococci.
Imipenem (Imp)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
8
I
I
4
S
S
2
S
S
NOTE: 1. Enterococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
2. Staphylococci therapy based on CLSI M100-S22.
3. Use for EUCAST Blended panel class.
4. For S. aureus and S. lugdunensis if Oxacillin MIC is >2 and/or Cefoxitin Screen >4, report Imipenem as
resistant regardless of MIC.
5. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Imipenem as resistant regardless of MIC.
6. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than
S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Imipenem as resistant regardless of MIC. For
additional information refer to Cefoxitin Screen section in the front of the guide.
7. Do not report drug, therapy or MIC for E. faecium and E. faecium group.
8. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
9. Do not report therapy for viridans streptococci (S. bovis group).
10. For beta-hemolytic streptococci, refer to Penicillin result.
9020-7493B
Page 89 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
3.
4.
5.
6.
7.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
N/R
2
S
1
S
Therapy based on EUCAST V3.1.
Use for PC36 and PM31 panels.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Imipenem
as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Imipenem as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other than S.
lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Imipenem as resistant regardless of MIC. For
additional information refer to Cefoxitin Screen section in the front of the guide.
Do not report drug, therapy or MIC for E. faecium and E. faecium group.
For staphylococci, refer to Cefoxitin Screen and/or the Oxacillin result.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for viridans streptococci (S. bovis group).
For beta-hemolytic streptococci, refer to Penicillin result.
Based on EUCAST interpretive guidelines for enterococci, all MICs of >2 will report as N/R, since
these dilutions do not differentiate between S, I and R (S4, I=8, R>8).
Imipenem (Imp)
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
I
4
S
2
S
1
S
Therapy based on CLSI M100-S22.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report Imipenem
as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Imipenem as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Imipenem as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
For streptococci, refer to Penicillin result.
Do not report drug, therapy or MIC for E. faecium and E. faecium group.
Kanamycin (K)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
16
I
8
S
4
S
2
S
NOTE: 1. Therapy based on SFM 2012.
2. Do not report drug, therapy or MIC for all streptococci (including beta-hemolytic streptococci (S.
agalactiae)), except viridans streptococci (S. bovis group).
9020-7493B
Page 90 of 158
NOTE: 1.
2.
3.
4.
5.
6.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
R
4
R
I
R
I
2
I
S
I
S
1
S
S
S
S
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci and viridans streptococci therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for PBC33 and PM32 panels.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Levofloxacin (Lvx)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
N/R
2
I
S
I
S
1
S
S
S
S
Staphylococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Enterococci and viridans streptococci therapies based on CLSI M100-S22.
Use for PBC33 and PM32 panels.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for enterococci all MICs of >2 will report as R, since these
dilutions do not differentiate between I and R (S2, I=4, R8).
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >2 will report as N/R, since
these dilutions do not differentiate between I and R (S2, I=4, R8).
Levofloxacin (Lvx)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
4
R
R
2
I
I
1
S
S
0.5
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for the EUCAST panel class.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Levofloxacin (Lvx)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
4
R
I
I
2
I
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based CLSI M100-S22.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
9020-7493B
Page 91 of 158
MIC
Lincomycin (Lin)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
4
R
I
I
2
N/R
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
3. Based on CLSI interpretive guidelines for staphylococci, all MICs of 2 will report as N/R, since these
dilutions do not differentiate between S and I (S1, I=2, R4).
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
8
I
I
I
4
I
I
I
2
S
S
S
1
S
S
S
NOTE: 1. Therapy based on SFM 2012.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Linezolid (Lzd)
NOTE: 1.
2.
3.
4.
5.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
R
R
R
>
4
S
S
I
2
S
S
S
S
1
S
S
S
S
0.5
S
S
S
S
Staphylococci, enterococci and beta-hemolytic streptococci therapies based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
The CLSI interpretative guideline for Linezolid with viridans streptococci is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for viridans streptococci, no
interpretations will be provided if the result is >2.
Linezolid (Lzd)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
R
R
R
>
4
S
S
I
2
S
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
9020-7493B
Page 92 of 158
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
R
>
4
S
I
2
S
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
3. The CLSI interpretative guidelines for Linezolid with streptococci is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for streptococci, no interpretations will
be provided if the result is >2.
Meropenem (Mer)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
N/R
8
I
N/R
4
S
N/R
2
S
N/R
NOTE: 1. Enterococci therapy based on EUCAST V3.1.
2. Staphylococci and streptococci therapies based on CLSI M100-S22.
3. Use for EUCAST Blended panel class
4. Only systemic therapy will be reported.
5. For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Meropenem as resistant regardless of MIC.
6. For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Meropenem as resistant regardless of
MIC.
7. For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Meropenem as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
8. Do not report drug, therapy or MIC for L. monocytogenes, all streptococci, except beta-hemolytic
streptococci (S. agalactiae) and viridans streptococci (S. bovis group).
9. For streptococci, refer to Penicillin result.
10. The CLSI interpretative guideline for Meropenem with beta-hemolytic and viridans streptococci is 0.5
for susceptible. Because intermediate and resistant interpretations have not been defined for
streptococci, all MICs of 2 will report as N/R, since these dilutions do not differentiate between S and
NS.
9020-7493B
Page 93 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
4.
5.
4.
ENTEROCOCCI
STREPTOCOCCI
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
R
>
1
N/R
Therapy based on EUCAST V3.1.
Use for PM31 panel.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for beta-hemolytic streptococci (S. agalactiae)
Based on EUCAST interpretive guidelines for staphylococci, all MICs of 1 will report as N/R since
these dilutions do not differentiate between S and I (S0.5, I=1, R>1).
Minocycline (Min)
NOTE: 1.
2.
3.
STAPHYLOCOCCI
>
R
N/R
8
I
N/R
4
S
N/R
2
S
N/R
1
S
N/R
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Meropenem as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Meropenem as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Meropenem as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
Do not report drug, therapy or MIC for L. monocytogenes
For streptococci, refer to Penicillin result.
The CLSI interpretative guideline for Meropenem with beta-hemolytic and viridans streptococci is 0.5
for susceptible. Because intermediate and resistant interpretations have not been defined for
streptococci, all MICs of 1 will report as N/R, since these dilutions do not differentiate between S and
NS.
Minocycline (Min)
NOTE: 1.
2.
3.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
R
R
>
8
I
I
4
S
S
2
S
S
1
S
S
Therapy based on CLSI M100-S22.
Use for PM33C and PM33E.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for beta-hemolytic streptococci (S. agalactiae).
9020-7493B
Page 94 of 158
NOTE: 1.
2.
3.
4.
5.
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
>
4
I
2
S
1
S
0.5
S
Therapy based on FDA approved breakpoints.
Only systemic therapy will be reported.
Use for PBC20, PBC23, PC29, PC33, PC34, PM26 and PM29 panels.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Moxifloxacin (Mxf)
NOTE:
STAPHYLOCOCCI
R
>
2
R
1
I
0.5
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes and PBC27, PBC28, PBC29, PM28, and PM33C
panels.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Do not report therapy for beta-hemolytic streptococci (S. agalactiae).
Moxifloxacin (Mxf)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
R
>
2
I
1
I
0.5
I
0.12
S
1. Therapy based on MENSURA.
2. Only systemic therapy will be reported.
3. Use for PM21 panel.
Mupirocin (Mup)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
I
I
S
S
ENTEROCOCCI
STREPTOCOCCI
R
>
256
8
4
S
NOTE: 1. Therapy based on manufacturers guidelines.
2. Breakpoints for skin infection isolates are 4, susceptible; 8, resistant. Breakpoints for nasal colonizing
isolates are 256 susceptible, 512 resistant. The Mupirocin category interpretations differ if the MIC is 8 or
256 and an alert will trigger.
3. Do not report drug, therapy or MIC for S. saprophyticus.
9020-7493B
Page 95 of 158
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
>
256
S
Therapy based on manufacturers guidelines for nasal colonization isolates.
Use for PC42C, PC42E, PM33C and PM33E panels.
Based on manufacturers guidelines with susceptible 4 and resistant 8, panel dilutions do not allow
reporting for skin infection isolates.
Do not report drug, therapy or MIC for S. saprophyticus.
Netilmicin (Nt)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
N/R
4
S
2
S
NOTE: 1. Enterococci and streptococci therapies based on EUCAST V3.1.
2. Staphylococci therapy based on CLSI M100-S22.
3. Use for EUCAST Blended panel class.
4. Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results can
occur.
5. Based on CLSI interpretive guidelines for staphylococci, all MICs of >4 will report as N/R, since these
dilutions do not differentiate between S, I and R (S8, I=16, R32).
Netilmicin (Nt)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
16
I
8
S
4
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for enterococci and L. monocytogenes because dangerously misleading results can
occur.
Nitrofurantoin (Fd)
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
64
S
S
32
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Only urine therapy will be reported.
Do not report drug, therapy or MIC for all streptococci, including beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Nitrofurantoin (Fd)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
64
I
I
32
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only urine therapy will be reported.
3. Do not report drug, therapy or MIC for all streptococci, including beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
9020-7493B
Page 96 of 158
MIC
STAPHYLOCOCCI
>
R
8
I
4
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only urine therapy will be reported.
Ofloxacin (Ofl)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
I
S
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
4
R
2
R
1
S
0.5
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Ofloxacin (Ofl)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
4
I
I
2
S
S
NOTE: 1. Therapy based on CLSI (NCCLS) M100-S14.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Oxacillin (Ox)
NOTE: 1.
2.
3.
4.
5.
MIC
S. AUREUS &
S. LUGDUNENSIS
OTHER
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
2
S
R
1
S
R
0.5
S
R/S*
0.25
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
For panels containing the Cefoxitin Screen, all staphylococci report Oxacillin as resistant if the
Cefoxitin Screen is >4. See Cefoxitin Screen information in the front of the therapy guide.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Oxacillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is <4 and Oxacillin MIC is 0.5, report Oxacillin as susceptible (S*).
For additional information refer to Cefoxitin Screen section in the front of the therapy guide.
9020-7493B
Page 97 of 158
NOTE: 1.
2.
3.
4.
3.
4.
5.
6.
7.
8.
S. AUREUS &
S. LUGDUNENSIS
OTHER
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
4
R
R
2
S
R
1
S
R
0.5
S
R/ S*
0.25
S
S
Therapy based on CLSI M100-S22.
For panels containing the Cefoxitin Screen, all staphylococci report Oxacillin as resistant if the
Cefoxitin Screen is >4. See Cefoxitin Screen information in the front of the guide.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Oxacillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is <4 and Oxacillin MIC is 0.5, report Oxacillin as susceptible (S*).
For additional information refer to Cefoxitin Screen section in the front of the guide.
Penicillin (P)
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
8
R
S
R
2
R
S
I
S
0.25
R
S
I
S
0.12
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci therapy based on EUCAST V3.1.
Enterococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100-S22.
L. monocytogenes therapies based on CLSI M45-A2
Use for PC38 panel.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >2.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >2 will report as R, since
these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
9020-7493B
Page 98 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
3.
4.
5.
6.
7.
8.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
2
R
S
I
S
0.25
R
S
I
S
0.12
S
S
S
S
S
0.06
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci therapy based on EUCAST V3.1.
Enterococci, bta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100-S22.
L. monocytogenes therapies based on CLSI M45-A2
Use for PBC33, PC35 and PM32 panels.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >2.
Based on CLSI interpretive guidelines for enterococci, all MICs of >2 will report as R, since these
dilutions do not differentiate between S and R (S8, R16).
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >2 will report as R, since
these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
Penicillin (P)
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
N/R
8
R
S
N/R
0.12
S
S
S
S
S
0.06
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci therapy based on EUCAST V3.1.
Enterococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100-S22.
L. monocytogenes therapies based on CLSI M45-A2.
Use for PBC32 panel.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >0.12.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >0.12 will report as N/R,
since these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
9020-7493B
Page 99 of 158
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
3.
4.
5.
6.
7.
8.
9.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
8
R
S
R
0.25
R
S
I
S
0.12
S
S
S
S
S
Staphylococci therapy based on EUCAST V3.1.
Enterococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100-S22.
L. monocytogenes therapies based on CLSI M45-A2.
Use for PM33E panel.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >0.25.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >0.25 will report as R, since
these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
Penicillin (P)
NOTE: 1.
2.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
N/R
0.25
R
S
I
S
0.12
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci therapy based on EUCAST V3.1.
Enterococci, beta-hemolytic streptococci and viridans streptococci therapies based on CLSI M100-S22.
L. monocytogenes therapies based on CLSI M45-A2.
Use for PC37 and PC42E panels.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic
streptococci, no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >0.25.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >0.25 will report as N/R,
since these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
Based on CLSI interpretive guidelines for enterococci, all MICs of >0.25 will report as R, since these
dilutions do not differentiate between S and R (S8, R16).
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
5.
6.
7.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
16
R
1
R
0.5
R
0.25
N/R
Therapy based on EUCAST V3.1.
Use for PC30 panel.
Do not report drug, therapy or MIC for all streptococci.
Do not report therapy for L. monocytogenes.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 and/or Cefoxitin Screen >4, report Penicillin as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Penicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
Based on EUCAST interpretive guidelines for staphylococci, all MICs of 0.25 will report as N/R, since
these dilutions do not differentiate between S and R (S0.12, R>0.25).
Penicillin (P)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
2
R
0.25
R
0.12
S
0.06
S
0.03
S
Therapy based on EUCAST V3.1.
Use for PC36 and PM31 panels.
Do not report drug, therapy or MIC for all streptococci.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 and/or Cefoxitin Screen >4, report Penicillin as
resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is >0.25 and/or Cefoxitin Screen >4, report
Penicillin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Penicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
guide.
Do not report therapy for L. monocytogenes.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
8
R
S
R
4
R
S
R
2
R
S
I
S
1
R
S
I
S
0.5
R
S
I
S
0.25
R
S
I
S
0.12
S
S
S
S
S
0.06
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci, Enterococci, beta-hemolytic streptococci, and viridans streptococci therapy based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Penicillin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Penicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
If beta-lactamase positive, report Penicillin as Blac regardless of MIC.
For enterococci, if beta-lactamase positive, report Penicillin as Blac regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci,
no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations will
be provided if the result is >2.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
2.
3.
4.
5.
6.
7.
8.
9.
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
8
R
S
N/R
0.12
S
S
S
S
S
0.06
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci, Enterococci, beta-hemolytic streptococci, and viridans streptococci therapy based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Penicillin as resistant regardless of
MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Penicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
If beta-lactamase positive, report Penicillin as Blac regardless of MIC.
For enterococci, if beta-lactamase positive, report Penicillin as Blac regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci,
no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no
interpretations will be provided if the result is >0.12.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >0.12 will report as N/R,
since these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
Penicillin (P)
NOTE: 1.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
R
8
R
S
R
2
R
S
I
S
0.25
R
S
I
S
0.12
S
S
S
S
S
0.06
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci, Enterococci, beta-hemolytic streptococci, and viridans streptococci therapy based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Penicillin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Penicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
If beta-lactamase positive, report Penicillin as Blac regardless of MIC.
For enterococci, if beta-lactamase positive, report Penicillin as Blac regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci,
no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations will
be provided if the result is >2.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >2 will report as R, since
these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
MIC
4.
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
L. monocytogenes
>
R
R
N/R
0.25
R
S
I
S
0.12
S
S
S
S
S
0.03
S
S
S
S
S
Staphylococci, Enterococci, beta-hemolytic streptococci, and viridans streptococci therapy based on
CLSI M100-S22. L. monocytogenes therapies based on CLSI M45-A2
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Penicillin as resistant regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS)
other than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Penicillin as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the
therapy guide.
If beta-lactamase positive, report Penicillin as Blac regardless of MIC.
For enterococci, if beta-lactamase positive, report Penicillin as Blac regardless of MIC.
The CLSI interpretative guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined for beta-hemolytic streptococci,
no interpretations will be provided if the result is >0.12.
The CLSI interpretative guideline for Penicillin with L. monocytogenes is 2 for susceptible. Because
intermediate and resistant interpretations have not been defined for L. monocytogenes, no interpretations will
be provided if the result is >0.25.
Based on CLSI interpretive guidelines for viridans streptococci, all MICs of >0.25 will report as N/R,
since these dilutions do not differentiate between I and R (S0.12, I=0.25-2, R4).
Based on CLSI interpretive guidelines for enterococci, all MICs of >0.25 will report as R, since these
dilutions do not differentiate between S and R (S8, R16).
Piperacillin-Tazobactam
(P/T)
NOTE: 1.
2.
3.
STAPHYLOCOCCI
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
S
4
S
2
S
1
S
Therapy based on CLSI M100-S22.
Do not report drug, therapy or MIC, for CNS with an MIC 0.5 for oxacillin or CfxS >4.
Do not report drug, therapy or MIC, for S. aureus and S. lugdunensis with an MIC >2 for Oxacillin or
CfxS >4.
For non-beta-lactamase producing enterococci, refer to Penicillin result.
Pristinamycin (Prs)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
2
I
I
I
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on SFM 2012.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
16
I
I
8
I
I
4
I
S
1
I
S
0.5
S
S
NOTE: 1. Therapy based on SFM 2008.
2. Use for the EUCAST panel class.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Rifampin (Rif)
MIC
STAPHYLOCOCCI
>
R
2
I
1
S
0.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
Synercid (Syn)
(Quinupristin/Dalfopristin)
NOTE: 1.
2.
3.
4.
5.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
I
S
S
E. faecium
ENTEROCOCCI
(other than E. faecium)
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
R
R
R
R
>
4
R
I
R
R
2
I
I
I
I
1
S
S
S
S
Staphylococci and E. faecium therapies based on EUCAST V3.1.
Enterococci (except E. faecium) and streptococci therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class.
It is important to speciate strains of enterococci, since Synercid is not active against E. faecalis.
Do not report therapy for viridans streptococci (S. bovis group).
Synercid (Syn)
(Quinupristin/Dalfopristin)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
(E. faecium only)
STREPTOCOCCI
R
R
>
4
R
I
2
I
I
1
S
S
0.5
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for EUCAST panel class, except for PC30 panel.
3. It is important to speciate strains of enterococci, since Synercid is not active against E. faecalis.
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
(E. faecium only)
STREPTOCOCCI
R
R
>
2
I
I
1
S
S
0.5
S
S
0.25
S
S
Therapy based on EUCAST V3.1.
Use for PC30 panel.
It is important to speciate strains of enterococci, since Synercid is not active against E. faecalis.
Based on EUCAST interpretive guidelines for E. faecium, all MICs of >2 will report as R, since these
dilutions do not differentiate between I and R (S1, I=2-4, R>4).
Synercid (Syn)
(Quinupristin/Dalfopristin)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
R
R
R
>
4
R
R
R
2
I
I
I
1
S
S
S
0.5
S
S
S
0.25
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. It is important to speciate strains of enterococci, since Synercid is not active against E. faecalis.
3. Do not report therapy for viridans streptococci (S. bovis group).
Teicoplanin (Tei)
NOTE: 1.
2.
3.
4.
5.
MIC
S. AUREUS
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
R
R
R
>
8
R
S
R
4
R
S
R
2
S
S
S
1
S
S
S
S. aureus and enterococci therapies based on EUCAST V3.1.
Staphylococci (except S. aureus) therapy based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for PC42E and PM33E panels.
Do not report drug, therapy or MIC for S. haemolyticus.
Based on CLSI interpretive guidelines for staphylococci (except S. aureus), all MICs of >8 will report
as R, since these dilutions do not differentiate between I and R (S8, I=16, R32).
Teicoplanin (Tei)
MIC
S. AUREUS
STAPHYLOCOCCI
ENTEROCOCCI
R
R
>
16
R
I
8
R
S
4
R
S
2
S
S
1
S
S
NOTE: 1. S. aureus and enterococci therapies based on EUCAST V3.1.
2. Staphylococci (except S. aureus) therapy based on CLSI M100-S22.
3. Use for PC42E and PM33E panels.
9020-7493B
STREPTOCOCCI
R
R
R
R
S
S
MIC
S. AUREUS
COAGULASE
NEGATIVE
STAPHYLOCOCCI
ENTEROCOCCI
ENTEROCOCCI
STREPTOCOCCI
STREPTOCOCCI
R
R
>
8
R
R
4
R
R
2
S
S
1
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for the EUCAST panel class.
3. Do not report drug, therapy or MIC for all coagulase negative staphylococci (CNS).
Teicoplanin (Tei)
MIC
STAPHYLOCOCCI
R
>
16
I
8
S
4
S
2
S
1
S
NOTE: 1. Therapy based on CLSI M100-S22.
Tetracycline (Te)
NOTE: 1.
2.
3.
4.
5.
6.
MIC
STAPHYLOCOCCI
R
I
S
S
S
S
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
N/R
2
I
S
I
S
1
S
S
S
S
Staphylococci and beta-hemolytic streptococci (S. agalactiae) therapies based on EUCAST V3.1.
Enterococci and viridans streptococci therapies based on CLSI M100-S22.
Use for EUCAST Blended panel class, except for PC38, PC42E and PM33E panels.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Based on CLSI interpretive guidelines for enterococci all MICs of >2 will report as R, since these
dilutions do not differentiate S, I and R (S4, I=8, R16).
Based on CLSI interpretive guidelines for viridans streptococci all MICs of >2 will report as N/R, since
these dilutions do not differentiate I and R (S2, I=4, R8).
Tetracycline (Te)
NOTE: 1.
2.
3.
4.
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
R
8
R
I
R
R
4
R
S
R
I
2
I
S
I
S
1
S
S
S
S
Staphylococci and beta-hemolytic streptococci (S. agalactiae) therapies based on EUCAST V3.1.
Enterococci and viridans streptococci therapies based on CLSI M100-S22.
Use for PC38, PC42E and PM33E panels.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
8
R
R
4
N/R
N/R
Therapy based on EUCAST V3.1.
Use for PC30 panel.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Based on EUCAST interpretive guidelines for staphylococci and beta-hemolytic streptococci, all MICs of
4 will report as N/R, since these dilutions do not differentiate between S, I and R (S1, I=2, R>2).
Tetracycline (Te)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
8
R
R
4
R
R
2
I
I
1
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Use for PC36 and PM31 panels.
3. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Tetracycline (Te)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
8
I
I
R
4
S
S
I
2
S
S
S
1
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
Tetracycline (Te)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
8
I
I
R
4
S
S
N/R
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
3. Based on CLSI interpretive guidelines for streptococci, all MICs of 4 will report as N/R, since these
dilutions do not differentiate between S and I (S2, I=4, R8).
9020-7493B
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
S
Therapy based on CLSI M100-S22.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2 or Cefoxitin Screen (CfxS) is >4, report
Ticarcillin-K Clavulanate as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Ticarcillin-K Clavulanate as resistant
regardless of MIC.
For panels containing Cefoxitin Screen and Oxacillin with coagulase-negative staphylococci (CNS) other
than S. lugdunensis, if CfxS is >4 and/or Oxacillin MIC is 1, report Ticarcillin-K Clavulanate as resistant
regardless of MIC. For additional information refer to Cefoxitin Screen section in the front of the guide.
Tobramycin (To)
NOTE: 1.
2.
3.
4.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
R
4
R
2
R
1
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Do not report drug, therapy or MIC for beta-hemolytic streptococci. See notes for species names.
Do not report therapy for enterococci because dangerously misleading results can occur.
Tobramycin (To)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8
I
4
S
2
S
1
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for beta-hemolytic streptococci. See notes for species names.
3. Do not report therapy for enterococci because dangerously misleading results can occur.
TrimethoprimSulfamethoxazole (T/S)
NOTE: 1.
2.
3.
4.
5.
6.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8/152
R
4/76
I
2/38
S
1/19
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes, except for PC30 and PC36 panels
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
If TFG negative, report therapy as TFG for all gram-positive organisms.
Do not report therapy for enterococci.
Do not report drug, therapy or MIC for L. monocytogenes.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
7.
4.
5.
6.
7.
ENTEROCOCCI
STREPTOCOCCI
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
2/38
S
1/19
S
Therapy based on EUCAST V3.1.
Use for PC36 panel.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
If TFG negative, report therapy as TFG for all gram-positive organisms.
Do not report therapy for enterococci.
Do not report drug, therapy or MIC for L. monocytogenes.
Based on EUCAST interpretive guidelines for staphylococci, all MICs of >2/38 will report as R, since
these dilutions do not differentiate S, I and R (S2/38, I=4/76, R>4/76).
TrimethoprimSulfamethoxazole (T/S)
NOTE: 1.
2.
3.
4.
STAPHYLOCOCCI
>
R
8/152
R
2/38
S
Therapy based on EUCAST V3.1.
Use for PC30 panel.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S.
agalactiae) and viridans streptococci (S. bovis group).
If TFG negative, report therapy as TFG for all gram-positive organisms.
Do not report therapy for enterococci.
Do not report drug, therapy or MIC for L. monocytogenes.
Based on EUCAST interpretive guidelines for staphylococci, all MICs of >2/38 will report as R, since
these dilutions do not differentiate S, I and R (S2/38, I=4/76, R>4/76).
TrimethoprimSulfamethoxazole (T/S)
NOTE: 1.
2.
3.
MIC
MIC
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
8/152
R
4/76
R
2/38
S
1/19
S
0.5/9.5
S
0.06/1.14
S
Therapy based on CLSI M100-S22.
Do not report therapy for enterococci because dangerously misleading results can occur.
If TFG negative, report therapy as TFG for all gram-positive organisms.
Do not report drug, therapy or MIC for L. monocytogenes.
9020-7493B
NOTE: 1.
2.
3.
MIC
STAPHYLOCOCCI
(S. aureus)
COAGULASENEGATIVE
STAPHYLOCOCCI
ENTEROCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
(S. agalactiae)
VIRIDANS
STREPTOCOCCI
(S. bovis group)
>
R
R
R
R
R
16
R
R
R
R
R
8
R
R
R
R
R
4
R
S
S
R
R
2
S
S
S
S
S
1
S
S
S
S
S
0.5
S
S
S
S
S
0.25
S
S
S
S
S
Therapy based on EUCAST V3.1.
Use for EUCAST Blended and EUCAST panel classes.
Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S. agalactiae)
and viridans streptococci (S. bovis group).
Vancomycin (Va)
MIC
S. AUREUS
COAGULASE- NEGATIVE
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
16
R
I
I
8
I
I
I
4
I
S
S
2
S
S
S
1
S
S
S
S
0.5
S
S
S
S
0.25
S
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for all streptococci except for beta-hemolytic streptococci (S. agalactiae)
and viridans streptococci (S. bovis group).
3. The CLSI interpretative guideline for Vancomycin with streptococci is 1 for susceptible. Because
intermediate and resistant interpretations have not been defined for streptococci, no interpretations will be
provided if the result is >1.
Vancomycin (Va)
MIC
S. AUREUS
COAGULASE- NEGATIVE
STAPHYLOCOCCI
ENTEROCOCCI
STREPTOCOCCI
>
R
R
R
N/R
16
R
I
I
N/R
8
I
I
I
N/R
4
I
S
S
N/R
2
S
S
S
N/R
NOTE: 1. Therapy based on CLSI M100-S22.
2. Use for PBC20, PBC23, PC1A, PC20 and PC21 panels.
3. The CLSI interpretative guideline for Vancomycin with streptococci is 0.5 for susceptible. Because
intermediate and resistant interpretations have not been defined for streptococci, all MICs of 2 will
report as N/R, since these dilutions do not differentiate between S and NS.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
32
I
I
I
16
S
S
S
8
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
3. Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia and Y. pestis.
AmoxicillinK Clavulanate (Aug)
NOTE: 1.
2.
3.
4.
5.
3.
4.
3.
4.
5.
6.
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
B PSEUDOMALLEI
>
R
16/8
I
8/4
S
Therapy based on CLSI M100-S22.
Rapid results (<16 hrs) are not provided for Amoxicillin-K Clavulanate on Synergies plus Gram-Negative
panels. Results are available at 16-20 hours.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report drug, therapy or MIC for B. pseudomallei.
Ampicillin (Am)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
16/8
R
4/2
S
Therapy based on EUCAST V3.1.
Use for Synergies plus Neg Combo Type 3 panels and Synergies plus Neg/Urine Combo Type 4 panels
Rapid results (<16 hrs) are not provided for Amoxicillin-K Clavulanate on Synergies plus Gram-Negative
panels. Results are available at 16-20 hours.
Do not report drug, therapy or MIC for B. pseudomallei.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
V. CHOLERAE
>
R
16
I
8
S
4
S
2
S
Therapy based on CLSI M100-S22.
Do not report drug, therapy or MIC for P. vulgaris or Shigella spp. See back of therapy guide for species
names.
For the following groups, Citrobacter spp., Enterobacter spp., Klebsiella spp. or Providencia spp., do not
report rapid Synergies plus results (<16 hrs) for drug, therapy or MIC. Overnight results (16-20 hrs) can be
reported. See back of therapy guide for species names.
For rapid Synergies plus results (<16 hrs), intermediate and resistant MICs obtained for P. mirabilis must be
confirmed with overnight incubation (16-20 hours) of the Synergies plus panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, and V. cholerae.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
3.
4.
5.
6.
3.
4.
5.
NON-ENTEROBACTERIACEAE
(Acinetobacter spp. only)
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
I
I
I
8
S
S
S
Therapy based on CLSI M100-S19.
Rapid results (<16 hrs) are not provided for Aztreonam on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Aztreonam cannot be used as a Screening antimicrobial agent for extended-spectrum beta-lactamases
On Synergies plus panels, ESBL-a and ESBL-b can be used as Screening antimicrobial agents for
extended-spectrum beta-lactamases (ESBL), see information under ESBL-a and ESBL-b.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Acinetobacter spp., B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Cefazolin (Cfz)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
16/8
I
8/4
S
4/2
S
Therapy based on CLSI M100-S22.
Use for the Synergies plus Neg BP Combo Type 8 and Synergies plus Neg Combo Type 2 panels panels.
Do not report drug, therapy or MIC for the following groups: Citrobacter spp., Enterobacter spp., M. morganii,
Salmonella spp. or Shigella spp. See back of therapy guide for species names.
Do not report therapy for Acinetobacter spp. because according to the FDA approved pharmaceutical
manufacturers package insert, sufficient strains of Acinetobacter spp. have not been tested to establish
efficacy with Ampicillin-Sulbactam.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Aztreonam (Azt)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
I
8
S
Therapy based on CLSI M100-S19.
Use for Synergies plus Neg Combo Type 3 panels, Synergies plus Neg/Urine Combo Type 4 panels,
9020-7493B
NOTE: 1.
2.
3.
4.
4.
5.
3.
4.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
32
R
R
4
N/R
S
Therapy based on EUCAST V3.1.
Rapid results (<16 hrs) are not provided for Cefepime on Synergies plus Gram-Negative panels. Results
are available at 16-20 hours.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 4 will report as N/R, since
these dilutions do not differentiate between S and I (S8, I=16, R>16).
Cefepime (Cpe)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
16
I
8
S
Therapy based on CLSI M100-S19.
Use for the Synergies plus Neg BP Combo Type 7 and Synergies plus Neg Combo Type 2 panels.
Rapid results (<16 hrs) are not provided for Cefazolin for the Synergies plus Gram-Negative panels
listed in Note 2. Results are available 16-20 hours.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading
results can occur.
Cefepime (Cpe)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
16
I
I
I
8
S
S
S
Therapy based CLSI M100-S22.
Rapid results (<16 hrs) are not provided for Cefepime on Synergies plus Gram-Negative panels. Results
are available at 16-20 hours.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
8
S
S
4
S
S
NOTE: 1. Therapy based on CLSI M100-S19.
2. Use for the Synergies plus Neg/Urine Combo Type 4 and Synergies plus Neg BP Combo Type 8 panel.
3. Cefotaxime cannot be used as a Screening antimicrobial agent for extended-spectrum beta-lactamases
4. On Synergies plus panels, ESBL-a and ESBL-b can be used as Screening antimicrobial agents for
extended-spectrum beta-lactamases (ESBL), see information under ESBL-a and ESBL-b.
5. Do not report drug, therapy or MIC for Acinetobacter spp., C. freundii Group, E. cloacae, Klebsiella
spp., or Proteus spp. See back of therapy guide for species names.
6. For rapid Synergies plus results (<16 hrs), do not report drug, therapy or MIC for S. marcescens
with MICs of >32 (I, R).
7. For rapid Synergies plus results (<16 hrs), intermediate/resistant MICs obtained for S. marcescens
must be confirmed with overnight incubation (16-20 hrs) of the Synergies plus panels.
8. Do not report therapy for Y. pestis because dangerously misleading results can occur.
9. Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
10. Do not report therapy for P aeruginosa based on CLSI M100-S22.
Cefotaxime (Cft)
NOTE: 1.
2.
3.
5.
4.
6.
7.
8.
5.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
16
I
I
8
S
S
2
S
S
Therapy based on CLSI M100-S19.
Use for the Synergies plus Neg BP Combo Type 7, Synergies plus Neg/Urine Combo Type 2 and
Rapid results (<16 hrs) are not provided for Cefotaxime on the Synergies plus Gram-Negative
panels listed in Note 2. Results are available at 16-20 hours.
Cefotaxime cannot be used as a Screening antimicrobial agent for extended-spectrum beta
lactamases (ESBL) on Synergies plus panels.
On Synergies plus panels, ESBL-a and ESBL-b can be used as Screening antimicrobial agents for
extended-spectrum beta-lactamases (ESBL), see information under ESBL-a and ESBL-b.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
Do not report therapy for P. aeruginosa based on CLSI M100-S22.
Cefotaxime (Cft)
NOTE: 1.
2.
3.
4.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P AERUGINOSA
>
16
2
Therapy based on CLSI M100-S19.
For ESBL Confirmation only.
Rapid results (<16 hours) are not provided for Cefotaxime on Synergies plus Neg Combo Type 3
panels. Results are available at 16-20 hours.
Cefotaxime is a confirmation antimicrobial agent for extended-spectrum beta-lactamases (ESBL).
For overnight (16-20 hrs) results, see ESBL information in front of therapy guide.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE P AERUGINOSA
B PSEUDOMALLEI
>
16
2
NOTE: 1. For ESBL Confirmation only.
2. ECft is Cefotaxime. Rapid results (<16 hours) are not provided for ECft on Synergies plus Gramnegative panels. Results are available at 16-20 hours.
3. ECft is a confirmation antimicrobial agent for extended-spectrum beta-lactamases (ESBL). For
Overnight results (16-20 hrs), see ESBL information in front of guide.
Cefotaxime-K
Clavulanate (Cft/CA)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
4/4
0.5/4
NOTE: 1. On Synergies plus panels, Cefotaxime-K Clavulanate is a confirmation antimicrobial for extended
-spectrum beta-lactamases (ESBL). See ESBL information in front of guide.
2. Rapid results (<16 hrs) are not provided for Cefotaxime-K Clavulanate on the Synergies plus
Gram-Negative panels. Results are available at 16-20 hours.
Cefotetan (Ctn)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
32
I
16
S
Therapy based on CLSI M100-S22.
Rapid results (<16 hrs) are not provided for Cefotetan on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading
results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Cefoxitin (Cfx)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
16
I
8
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Rapid results (<16 hrs) are not provided for Cefoxitin on Synergies plus Gram-Negative
panels. Results are available 16-20 hours.
3. Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously
misleading results can occur.
Cefoxitin (Cfx)
NOTE: 1.
2.
3.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P AERUGINOSA
>
R
32
I
8
S
Therapy based on SFM 2012.
Use for Synergies plus Neg Combo Type 3 panels and Synergies plus Neg/Urine Combo Type 4
panels
Rapid results (<16 hrs) are not provided for Cefoxitin on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Page 116 of 158
NOTE: 1.
2.
3.
4.
5.
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
R
R
R
R
16
I
I
I
I
8
S
S
S
S
4
S
S
S
S
2
S
S
S
S
Therapy based on CLSI M100-S19.
For E. cloacae, do not report rapid Synergies plus results (<16 hrs) for drug, therapy or MIC.
Overnight results (16-20 hrs) can be reported.
Ceftazidime cannot be used as a Screening antimicrobial agent for extended-spectrum beta-lactamases
On Synergies plus panels, ESBL-a and ESBL-b can be used as screening antimicrobial agents for
extended-spectrum beta-lactamases (ESBL), see information under ESBL-a and ESBL-b.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
ESBL Confirm
Ceftazidime (ECaz)
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
P. AERUGINOSA
B. PSEUDOMALLEI
>
8
1
NOTE: 1. For ESBL Confirmation only.
2. ECaz is Ceftazidime. Rapid results (<16 hrs) are not provided for ECaz on Synergies plus GramNegative panels. Results are available at 16-20 hours.
3. ECaz is a confirmation antimicrobial agent for extended-spectrum beta-lactamases (ESBL). For
Dried Overnight results and ESBL Confirmation organisms, see ESBL information in front of guide.
Ceftazidime-K
Clavulanate (Caz/CA)
MIC
Ceftriaxone (Cax)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
2/4
0.25/4
NOTE: 1. Rapid results (<16 hrs) are not provided for Ceftazidime-K Clavulanate on Synergies plus GramNegative panels. Results are available 16-20 hours.
2. On Synergies plus panels, Ceftazidime-K Clavulanate is a confirmation antimicrobial for extendedspectrum beta-lactamases (ESBL). See ESBL information in front of guide.
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
32
I
I
8
S
S
Therapy based on CLSI M100-S19.
Do not report drug, therapy or MIC for P. vulgaris.
For Citrobacter spp. or E. cloacae, do not report rapid Synergies plus results (<16 hrs) for drug,
therapy or MIC. Overnight results (16-20 hrs) can be reported. See back of therapy guide for
species names.
Ceftriaxone cannot be used as a screening antimicrobial agent for extended-spectrum beta
lactamases (ESBL) on Synergies plus panels.
On Synergies plus panels, ESBL-a and ESBL-b can be used as screening antimicrobial agents for
extended-spectrum beta-lactamases (ESBL), see information under ESBL-a and ESBL-b.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia, B. pseudomallei, S. maltophilia and Vibrio spp.
Do not report therapy for P. aeruginosa based on CLSI M100-S22.
9020-7493B
NOTE: 1.
2.
3.
4.
4.
5.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
R
2
I
I
1
S
S
0.5
S
S
NOTE: 1. Therapy based on CLSI M100-S21.
2. Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
3. For Y. pestis therapy based on CLSI M100-S17 interpretive breakpoints.
Colistin (Cl)
3.
4.
P. AERUGINOSA
>
R
16
I
8
S
Therapy based on CLSI M100-S22.
Report for Urine source only.
Rapid results (<16 hrs) are not provided for Cephalothin on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading results
can occur.
Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia and Vibrio spp.
Ciprofloxacin (Cp)
NOTE: 1.
2.
P. AERUGINOSA
>
R
16
I
8
S
4
S
Therapy based on CLSI M100-S22.
For Enterobacter spp. or K. pneumoniae, do not report rapid Synergies plus results (<16 hrs) for drug,
therapy or MIC. Overnight results (16-20 hrs) can be reported. See back of therapy guide for species
names.
Do not report therapy for Salmonella/Shigella group and Y. pestis because dangerously misleading
results can occur.
The CLSI M100-S22 breakpoints for Enterobacteriaceae and Cefuroxime axetil (oral) are S4, R=816, R32.
Cephalothin (Cf)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
P AERUGINOSA
Y. PESTIS
R
I
S
S
R
I
S
S
PSEUDOMONAS SPP.
>
R
R
4
R
S
2
S
S
Therapy based on EUCAST V3.1.
Rapid results (<16 hrs) are not provided for Colistin on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Do not report therapy for Y. pestis.
Do not report drug, therapy or MIC for Salmonella species, E. cloacae or Acinetobacter species.
9020-7493B
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE P. AERUGINOSA
>
4
NOTE: 1. ESBL-a is Cefpodoxime. Rapid results (<16 hrs) are not provided for ESBL-a on Synergies plus
Gram-Negative panels. Results are available at 16-20 hours.
2. ESBL-a is a screening antimicrobial agent for extended-spectrum beta-lactamases (ESBL). For Dried
Overnight results and E. coli, K. oxytoca, K. pneumoniae and P. mirabilis, see ESBL information in
front of guide.
ESBL-b (ESb)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE P. AERUGINOSA
>
1
NOTE: 1. ESBL-b is Ceftazidime. Rapid results (<16 hrs) are not provided for ESBL-b on Synergies plus
Gram-Negative panels. Results are available at 16-20 hours.
2. ESBL-b is a screening antimicrobial agent for extended-spectrum beta-lactamases (ESBL). For Dried
Overnight results and E. coli, K. oxytoca, K. pneumoniae and P. mirabilis, see ESBL information in
front of therapy guide.
Fosfomycin (Fos)
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
32
S
S
NOTE: 1. Therapy based on EUCAST V1.3.
2. Rapid results (<16 hrs) are not provided for Fosfomycin on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
3. Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Gatifloxacin (Gat)
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
A. LWOFFII
P. AERUGINOSA
>
R
R
4
I
I
2
S
S
Therapy based on FDA approved breakpoints.
Use for the Synergies plus Neg BP Combo Type 7, Synergies plus Neg/Urine Combo Type 2,
Synergies plus Neg/Urine Combo Type 1 and Synergies plus Neg Combo Type 2 panels.
Do not report drug, therapy or MIC for P. aeruginosa and Non-Enterobacteriaceae, except A. lwoffii.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Gentamicin (Gm)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
Y. PESTIS
>
R
R
R
R
8
I
I
I
I
4
S
S
S
S
2
S
S
S
S
1
S
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
3. Do not report therapy for B. cepacia, B. pseudomallei and S. maltophilia.
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
NONENTEROBACTERIACEAE
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
R
4
I
2
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for B. pseudomallei and Y. pestis.
Levofloxacin (Lvx)
MIC
ENTEROBACTERIACEAE
R
I
S
ACINETOBACTER SPP.
R
I
S
P. AERUGINOSA
R
I
S
PSEUDOMONAS SPP.
>
R
R
R
4
R
R
R
1
S
S
S
0.5
S
S
S
Therapy based on EUCAST V3.1.
Rapid results (<16 hrs) are not provided for Levofloxacin on Synergies plus Neg Combo Type 3
panels. Results are available at 16-20 hours.
Do not report therapy for Y. pestis.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, Acinetobacter spp. and
Pseudomonas spp., all MICs of >1 will report as R, since these dilutions do not differentiate between
I and R (S1, I=2, R>2).
NOTE: 1.
2.
3.
4.
5.
Meropenem (Mer)
4.
5.
B. PSEUDOMALLEI
>
R
R
R
8
I
I
I
4
S
S
S
Therapy based on CLSI M100-S19.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and S. maltophilia.
For Acinetobacter spp., susceptible and intermediate results will not be reported.
Levofloxacin (Lvx)
NOTE: 1.
2.
3.
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
I
I
I
4
S
S
S
Therapy based on CLSI M100-S19.
Use for the Synergies plus Neg BP Combo Type 7 and Synergies plus Neg Combo Type 2 panels.
For P. aeruginosa, do not report rapid Synergies plus results (<16 hrs) drug, therapy or MIC.
Overnight results (16-20 hrs) can be reported.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. pseudomallei and S. maltophilia.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
3.
4.
5.
3.
4.
5.
P AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
64
I
32
S
Therapy based on CLSI M100-S22.
Use for the Synergies plus Neg/Urine Combo Type 1 and Synergies plus Neg/Urine Combo Type 2
panels.
Rapid results (<16 hrs) are not provided for Nitrofurantoin on the Synergies plus Gram-Negative
panels listed in Note 2. Results are available at 16-20 hours.
Only urine therapy will be reported.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
Norfloxacin (Nxn)
NOTE: 1.
2.
3.
4.
NON-ENTEROBACTERIACEAE
>
R
64
I
32
S
16
S
Therapy based on CLSI M100-S22.
Use for the Synergies plus Neg BP Combo Type 7, Synergies plus Neg BP Combo Type 8
Nitrofurantoin (Fd)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
16
I
8
S
Therapy based on SFM 2012.
Only urine therapy will be reported.
Rapid results (<16 hrs) are not provided for Nalidixic Acid on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Do not report drug, therapy or MIC for E. cloacae and K. pneumoniae.
Do not report therapy for Salmonella because the ability of the Synergies plus panels to detect
Nalidixic Acid resistance in Salmonella strains is unknown, resistant strains were not available at the
time of comparative testing. An alternate method should be used.
Nitrofurantoin (Fd)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
8
I
I
I
4
S
S
S
Therapy based on CLSI M100-S22.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
4.
5.
6.
3.
4.
5.
6.
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
64
R
R
16
I
S
8
S
S
Therapy based on EUCAST
Rapid results (<16 hrs) are not provided for Piperacillin on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Do not report drug, therapy or MIC for C. koseri and S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp. and Plesiomonas shigelloides.
Piperacillin (Pi)
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
R
R
8
I
I
I
4
S
S
S
Therapy based on CLSI M100-S22.
Rapid results (<16 hrs) are not provided for Norfloxacin on the Synergies plus Gram-Negative panels
listed in Note 2. Results are available at 16-20 hours.
Only urine therapy will be reported.
Do not report therapy for Acinetobacter spp., Aeromonas spp., B. cepacia, B. pseudomallei,
Plesiomonas shigelloides, S. maltophilia, Vibrio spp. and Y. pestis.
Piperacillin (Pi)
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
S
32
I
I
S
16
S
S
S
Therapy based on CLSI M100-S21.
Use for the Synergies plus Neg BP Combo Type 8 and Synergies plus Neg/Urine Combo Type 1
panels.
Do not report drug, therapy or MIC for S. maltophilia or Citrobacter spp. See back of therapy guide for
species names.
For Acinetobacter spp., K. oxytoca, M. morganii or P. mirabilis, do not report rapid Synergies plus
results (<16 hrs) for drug, therapy or MIC. Overnight results (16-20 hrs) can be reported. See back of
therapy guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, and Plesiomonas
shigelloides.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
7.
8.
3.
4.
5.
6.
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
S
32
I
I
S
16
S
S
S
8
S
S
S
Therapy based on CLSI M100-S21.
Use for the Synergies plus Neg Combo Type 2, Synergies plus Neg BP Combo Type 8,
Synergies plus Neg Combo Type 3 and Synergies plus Neg/Urine Combo Type 4 panels.
Do not report drug, therapy, or MIC for S. maltophilia and Acinetobacter spp. See back of therapy guide for
species names.
For Citrobacter spp. or Enterobacter spp., do not report rapid Synergies plus results (<16 hrs) for drug,
therapy or MIC. Overnight results (16-20 hrs) can be reported. See back of therapy guide for species
names.
For rapid Synergies plus results (<16 hrs), do not report drug, therapy or MIC for Serratia spp. with MICs of
32 (I, R).
For rapid Synergies plus results (<16 hrs), intermediate/resistant MICs obtained for Serratia spp. must be
confirmed with overnight incubation (16-20 hrs) of the Synergies plus panels.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and B. pseudomallei.
Piperacillin-Tazobactam
(P/T)
NOTE: 1.
2.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
I
16
S
S
S
Therapy based on CLSI M100-S22
Use for the Synergies plus Neg BP Combo Type 7, Synergies plus Neg/Urine Combo Type 1 and
Rapid results (<16 hrs) are not provided for Piperacillin-Tazobactam on the Synergies plus GramNegative panels listed in Note 2. Results are available at 16-20 hours.
Do not report drug, therapy or MIC for S. maltophilia and Acinetobacter spp. See back of therapy
guide for species names.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for B. cepacia and B. pseudomallei.
Tetracycline (Te)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
>
8
4
2
R
I
S
S
R
I
S
S
MIC
B. PSEUDOMALLEI
Y. PESTIS
P. AERUGINOSA
V. CHOLERAE
>
R
R
8
I
I
4
S
S
2
S
S
NOTE: 1. Enterobacteriaceae (except V. cholerae and Y. pestis) and Non-Enteroacteriaceae (except B.
pseudomallei) therapies based on CLSI M100-S22. B. pseudomallei and Y. pestis therapies based
on CLSI M45-A2.
2. Use these tables for the Synergies plus Neg BP Combo Type 8 and Synergies plus Neg/Urine
Combo Type 1 panels.
3. Do not report therapy for B. cepacia, S. maltophilia and V. cholerae.
9020-7493B
4.
5.
6.
7.
4.
5.
6.
3.
4.
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
MIC
ENTEROBACTERIACEAE
ACINETOBACTER SPP.
PSEUDOMONAS SPP.
>
R
R
64
R
R
16
N/R
S
Therapy based on EUCAST V3.1.
Use for Synergies plus Neg Combo Type 3 panels and Synergies plus Neg/Urine Combo Type 4 panels.
Rapid results (<16 hrs) are not provided for Ticarcillin-K Clavulanate on Synergies plus Gram-Negative
panels. Results are available at 16-20 hours.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 16 will report as N/R,
since these dilutions do not differentiate between S and I (S8, I=16, R>16).
NOTE: 1.
2.
ENTEROBACTERIACEAE
>
R
R
64
R
R
16
N/R
S
Therapy based on EUCAST V3.1.
Use for Synergies plus Neg Combo Type 3 panels and Synergies plus Neg/Urine Combo Type 4 panels.
Rapid results (<16 hrs) are not provided for Ticarcillin on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Do not report drug, therapy, or MIC for S. maltophilia.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides and Vibrio spp.
Based on EUCAST interpretive guidelines for Enterobacteriaceae, all MICs of 16 will report as N/R,
since these dilutions do not differentiate between S and I (S8, I=16, R>16).
NOTE: 1.
2.
3.
NOTE: 1.
2.
3.
MIC
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
R
R
64
I
I
S
16
S
S
S
Therapy based on CLSI M100-S21.
Rapid results (<16 hrs) are not provided for Ticarcillin-K Clavulanate on Synergies plus GramNegative panels. Results are available at 16-20 hours.
Do not report therapy for Y. pestis because dangerously misleading results can occur.
Do not report therapy for Aeromonas spp., B. pseudomallei, Plesiomonas shigelloides and Vibrio spp.
Tobramycin (To)
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P AERUGINOSA
>
R
R
R
8
I
I
I
4
S
S
S
2
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report therapy for Salmonella/Shigella group because dangerously misleading results can occur.
3. Do not report therapy for Aeromonas spp., B. cepacia, B. pseudomallei, Plesiomonas shigelloides, S.
maltophilia, Vibrio spp. and Y. pestis.
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
ENTEROBACTERIACEAE
NON-ENTEROBACTERIACEAE
P. AERUGINOSA
>
R
8
S
Therapy based on CLSI M100-S22.
Rapid results (<16 hrs) are not provided for Trimethoprim on Synergies plus Gram-Negative panels.
Results are available at 16-20 hours.
Only urine therapy will be reported.
Do not report therapy for Aeromonas spp., Plesiomonas shigelloides, Vibrio spp. and Y. pestis.
TrimethoprimSulfamethoxazole (T/S)
MIC
ENTEROBACTERIACEAE
2/38
>
R
S
MIC
B PSEUDOMALLEI
NON-ENTEROBACTERIACEAE
P AERUGINOSA
R
S
Y PESTIS
>
R
R
S
S
Therapy based on CLSI M100-S22.
For rapid Synergies plus panel results (<16 hrs), do not report drug, therapy or MIC for P. aeruginosa.
For overnight results (16-20 hours), do not report therapy for P. aeruginosa.
Do not report therapy for V. cholerae, sufficient strains were not tested to establish efficacy. Interpretive
breakpoints should not be reported.
2/38
NOTE: 1.
2.
3.
4.
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
32
R
16
R
8
S
4
S
2
S
1
S
Therapy based on CLSI M100-S22.
Use for enterococci.
For enterococci, if beta-lactamase positive, report Ampicillin as Blac regardless of MIC.
The predicted interpretation for staphylococci will be based on the Penicillin and/or Oxacillin MICs.
Chloramphenicol (C)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
16
I
8
S
4
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
Clindamycin (Cd)
NOTE: 1.
2.
3.
4.
MIC
STAPHYLOCOCCI
R
I
S
S
ENTEROCOCCI
>
R
2
I
1
I
0.5
S
0.25
S
0.12
S
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Do not report drug, therapy or MIC for enterococci.
For staphylococci, if Erythromycin MIC is N/R and Clindamycin MIC is 2, do not report therapy.
Erythromycin (E)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
4
I
2
I
1
I
0.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
3. Do not report drug, therapy or MIC for enterococci.
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
8
I
4
S
2
S
1
S
0.5
S
0.25
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for enterococci.
Imipenem (Imp)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
(E. faecalis only)
>
R
8
I
4
S
2
S
1
S
0.5
S
NOTE: 1. Therapy based on FDA approved breakpoints for E. faecalis.
2. Do not report drug, therapy or MIC for enterococci (except for E. faecalis.)
3. The predicted interpretation for staphylococci will be based on the Penicillin and/or Oxacillin MICs.
Levofloxacin (Lvx)
MIC
STAPHYLOCOCCI
>
R
4
R
2
I
1
S
0.5
S
0.25
S
NOTE: 1. Therapy based on CLSI M100-S22.
Linezolid (Lzd)
MIC
MIC
ENTEROCOCCI
R
S
S
S
S
R
I
S
S
S
STAPHYLOCOCCI
>
R
64
I
32
S
16
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only urine therapy will be reported.
9020-7493B
R
I
S
S
S
S
STAPHYLOCOCCI
>
4
2
1
0.5
NOTE: 1. Therapy based on CLSI M100-S22.
Nitrofurantoin (Fd)
ENTEROCOCCI
ENTEROCOCCI
R
I
S
S
MIC
S. AUREUS &
S. LUGDUNENSIS
OTHER
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
2
S
R
1
S
R
0.5
S
R
0.25
S
S
0.12
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for enterococci.
3. For rapid results (<16 hours), do not report drug, therapy or MIC for S. aureus with Oxacillin MICs <4
and coagulase-negative staphylococci with Oxacillin MICs <0.5. Results are available at 16-20 hours.
Penicillin (P(E))
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
64
R
32
R
16
R
8
S
4
S
2
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Use for enterococci.
3. For enterococci, if beta-lactamase positive, report Penicillin as Blac regardless of MIC.
Penicillin (P(S))
NOTE: 1.
2.
3.
4.
5.
6.
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
0.12
S
0.06
S
0.03
S
Therapy based on CLSI M100-S22.
Use for staphylococci.
Do not report drug, therapy or MIC for S. saprophyticus.
For S. aureus and S. lugdunensis, if Oxacillin MIC is >2, report Penicillin as resistant regardless of MIC.
For CNS other than S. lugdunensis, if Oxacillin MIC is 0.5, report Penicillin as resistant regardless of MIC.
If beta-lactamase positive, report Penicillin as Blac regardless of MIC.
Rifampin (Rif)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
2
I
1
S
0.5
S
0.25
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for enterococci.
9020-7493B
MIC
STAPHYLOCOCCI
ENTEROCOCCI
(E. faecium)
R
R
>
2
I
I
1
S
S
0.5
S
S
0.25
S
S
0.12
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. It is important to speciate strains of enterococci, since Synercid is only active against E. faecium.
3. Do not report drug, therapy or MIC for all enterococci, except E. faecium.
Teicoplanin (Tei)
MIC
STAPHYLOCOCCI
ENTEROCOCCI
>
R
16
I
8
S
4
S
2
S
1
S
NOTE: 1. Therapy based on CLSI M100-S22.
Tetracycline (Te)
MIC
STAPHYLOCOCCI
R
I
S
S
S
S
ENTEROCOCCI
>
R
8
I
4
S
2
S
1
S
0.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
TrimethoprimSulfamethoxazole (T/S)
MIC
STAPHYLOCOCCI
R
I
S
S
S
S
ENTEROCOCCI
>
R
2/38
S
1/19
S
0.5/9.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Do not report drug, therapy or MIC for enterococci.
Vancomycin (Va)
MIC
S. aureus
COAGULASE- NEGATIVE
STAPHYLOCOCCI
ENTEROCOCCI
>
R
R
R
16
R
I
I
8
I
I
I
4
I
S
S
2
S
S
S
1
S
S
S
0.5
S
S
S
0.25
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. For rapid results (<16 hrs), do not report drug, therapy or MIC for S. aureus with MICs of 8 or 16.
Final results will be reported after overnight incubation (16-20 hrs).
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
4/2
I
2/1
S
1/0.5
S
Streptococci (Group A, B, C and G) and viridans streptococci therapies based on EUCAST V3.1.
S. pneumoniae therapy based on CLSI M100-S22.
Amoxicillin/
K Clavulanate (Aug)
MIC
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
4/2
2/1
1/0.5
0.5/0.25
0.25/0.12
NOTE: 1. Therapy based on EUCAST V3.1.
>
4/2
2/1
1/0.5
0.5/0.25
0.25/0.12
NOTE: 1. Therapy based on CLSI M100-S22.
Ampicillin (Am)
NOTE: 1.
2.
3.
4.
MIC
R
I
S
S
S
S
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
R
4
R
R
2
I
I
1
I
I
0.5
S
S
0.25
S
S
S
0.12
S
S
S
0.06
S
S
S
S. pneumoniae and viridans streptococci therapies based on EUCAST V3.1.
Beta-hemolytic streptococci therapy based on CLSI M100-S22.
9020-7493B
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
>
R
16
R
8
R
4
R
2
I
1
I
0.5
S
0.25
S
0.12
S
0.06
S
0.03
S
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
R
R
I
I
S
S
S
S
S
VIRIDANS
STREPTOCOCCI
>
R
8
R
4
I
2
I
1
I
0.5
I
0.25
S
S
0.12
S
S
0.06
S
S
0.03
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. The CLSI interpretative guideline for Ampicillin with beta-hemolytic streptococci is 0.25 for susceptible.
Because intermediate and resistant interpretations have not been defined, no interpretations will be
provided if the result is >0.25.
Azithromycin (Azi)
NOTE: 1.
2.
3.
4.
5.
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
R
2
R
R
R
1
R
R
I
0.5
I
I
S
0.25
S
S
S
0.12
S
S
S
S. pneumoniae and Streptococci (Group A, B, C and G) therapies based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
9020-7493B
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
R
R
4
R
R
R
2
R
R
R
1
I
I
I
0.5
S
S
S
0.25
S
S
S
0.12
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
3. Susceptibility and resistance to Azithromycin can be predicted by testing Erythromycin.
Cefaclor (Cfr)
MIC
S. PNEUMONIAE
>
16
8
4
2
1
0.5
NOTE: 1. Therapy based on CLSI M100-S22.
Cefepime (Cpe)
NOTE: 1.
2.
3.
4.
MIC
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
R
R
I
S
S
S. PNEUMONIAE
>
R
R
2
I
R
1
S
R
0.5
S
S
S
0.25
S
S
S
S. pneumoniae and viridans streptococci therapies based on EUCAST V3.1.
Beta-hemolytic streptococci therapy based on CLSI M100-S22.
Cefepime (Cpe)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
R
2
I
I
1
S
S
0.5
S
S
S
0.25
S
S
S
0.12
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. The CLSI interpretative guideline for Cefepime with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined, no interpretations will be
provided if the result is >0.5.
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
>
R
R
2
I
R
1
I
R
0.5
S
S
S
0.25
S
S
S
S. pneumoniae and viridans streptococci therapies based on EUCAST V3.1.
Beta-hemolytic streptococci therapy based on CLSI M100-S22.
Cefotaxime (Cft)
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
>
R
32
R
16
R
8
R
4
R
2
I
1
I
0.5
S
0.25
S
0.12
S
NOTE: 1. Therapy based on EUCAST V3.1.
NOTE: 1.
2.
3.
4.
VIRIDANS
STREPTOCOCCI
MIC
S. PNEUMONIAE
(Meningitis)
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
R
R
R
R
R
S
S
S
VIRIDANS
STREPTOCOCCI
>
R
R
8
R
R
4
R
R
2
R
I
1
I
S
0.5
S
S
S
0.25
S
S
S
0.12
S
S
S
0.06
S
S
S
0.03
S
S
S
Therapy based on CLSI M100-S22.
The CLSI interpretative guideline for Cefotaxime with beta-hemolytic streptococci is 0.5 for
susceptible. Because intermediate and resistant interpretations have not been defined, no
interpretations will be provided if the result is >0.5.
For S. pneumoniae, Cefotaxime breakpoints are based on isolates from CSF (meningitis). For all other
S. pneumoniae isolates report both meningitis breakpoints (S0.5, I=1, R2) and non-meningitis
breakpoints (S1, I=2, R4).
Results of testing Cefotaxime should be routinely reported for CSF isolates of S. pneumoniae.
9020-7493B
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
>
R
R
2
I
R
1
I
R
0.5
S
S
S
0.25
S
S
S
S. pneumoniae and viridans streptococci therapies based on EUCAST V3.1.
Beta-Hemolytic therapy based on CLSI M100-S22.
Ceftriaxone (Cax)
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
>
R
8
R
4
R
2
I
1
I
0.5
S
0.25
S
0.12
S
NOTE: 1. Therapy based on EUCAST V3.1.
NOTE: 1.
2.
3.
4.
VIRIDANS
STREPTOCOCCI
MIC
S. PNEUMONIAE
(Meningitis)
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
R
R
R
S
S
S
VIRIDANS
STREPTOCOCCI
>
R
R
2
R
I
1
I
S
0.5
S
S
S
0.25
S
S
S
Therapy based on CLSI M100-S22.
The CLSI interpretative guideline for Ceftriaxone with beta-hemolytic streptococci is 0.5 for susceptible.
Because intermediate and resistant interpretations have not been defined, no interpretations will be
provided if the result is >0.5.
For S. pneumoniae, Ceftriaxone breakpoints are based on isolates from CSF (meningitis). For all other
S. pneumoniae isolates report both meningitis breakpoints (S0.5, I=1, R2) and non-meningitis
breakpoints (S1, I=2, R4).
Results of testing Ceftriaxone should be routinely reported for CSF isolates of S. pneumoniae.
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
4
R
2
R
1
I
0.5
S
0.25
S
NOTE: 1. Therapy based on EUCAST V3.1.
R
R
R
R
S
S
9020-7493B
MIC
Chloramphenicol (C)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
8
R
4
R
2
R
1
I
0.5
S
0.25
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. The CLSI breakpoints for Cefuroxime axetil (oral) are S1, I=2, R4.
NOTE: 1.
2.
3.
4.
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
R
8
S
S
I
4
S
S
S
2
S
S
S
S. pneumoniae and streptococci (Group A, B, C, and G) therapies based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
Chloramphenicol (C)
MIC
S. PNEUMONIAE
>
R
16
R
8
S
4
S
2
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Only systemic therapy will be reported.
MIC
S. PNEUMONIAE
>
R
16
R
8
R
4
S
2
S
1
S
NOTE: 1. Therapy based on CLSI M100-S22
2. Only systemic therapy will be reported.
9020-7493B
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
R
R
S
S
S
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
I
S
S
S
R
R
I
S
S
S
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
4
2
1
0.5
0.25
0.12
0.06
NOTE: 1. Therapy based on CLSI M100-S22.
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
R
2
R
R
R
1
R
R
R
0.5
I
I
I
0.25
S
S
S
0.12
S
S
S
S. pneumoniae and streptococci (Group A, B, C and G) therapies based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
Clarithromycin (Cla)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
R
R
2
R
R
R
1
R
R
R
0.5
I
I
I
0.25
S
S
S
0.12
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Susceptibility and resistance to Clarithromycin can be predicted by testing Erythromycin.
Clindamycin (Cd)
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
>
R
R
4
R
R
2
R
R
1
R
R
0.5
S
S
0.25
S
S
0.12
S
S
0.06
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
2. Only systemic therapy will be reported.
9020-7493B
VIRIDANS
STREPTOCOCCI
R
R
R
R
S
S
S
S
MIC
S. PNEUMONIAE
>
R
2
R
1
R
0.5
I
0.25
S
0.12
S
0.06
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
Daptomycin (Dap)
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
R
I
S
S
S
R
R
R
I
S
S
S
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
2
R
1
S
S
0.5
S
S
0.25
S
S
Streptococci (Group A, B, C and G) therapy based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
Daptomycin (Dap)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
2
1
S
S
0.5
S
S
0.25
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. The CLSI interpretative guideline with beta-hemolytic and viridans streptococci is 1 for susceptible.
Because intermediate and resistant interpretations have not been defined, no interpretations will be
provided if the result is >1.
Erythromycin (E)
NOTE: 1.
2.
3.
4.
5.
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
R
0.5
I
I
I
0.25
S
S
S
0.12
S
S
S
0.06
S
S
S
S. pneumoniae and streptococci (Group A, B, C and G) therapies based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
4
R
R
2
R
R
1
R
R
0.5
N/R
N/R
Therapy based on EUCAST V3.1.
Only systemic therapy will be reported.
Erythromycin (E)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
R
R
4
R
R
R
2
R
R
R
1
R
R
R
0.5
I
I
I
0.25
S
S
S
0.12
S
S
S
0.06
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Only systemic therapy will be reported.
3. Susceptibility and resistance to Azithromycin and Clarithromycin can be predicted by testing Erythromycin.
Gatifloxacin (Gat)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS STREPTOCOCCI
>
2
1
0.5
0.25
0.12
NOTE: 1. Do not report drug, therapy or MIC.
Levofloxacin (Lvx)
MIC
S. PNEUMONIAE
>
R
R
R
4
R
R
I
2
S
I
S
1
S
S
S
0.5
S
S
S
NOTE: 1. S. pneumoniae and streptococci (Group A, B, C and G) therapies based on EUCAST V3.1.
2. Viridans streptococci therapy based on CLSI M100-S22.
9020-7493B
MIC
S. PNEUMONIAE
>
R
8
R
4
R
2
S
1
S
0.5
S
0.25
S
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
S. PNEUMONIAE
>
4
2
1
0.5
0.25
NOTE: 1. Therapy based on CLSI M100-S22.
Linezolid (Lzd)
NOTE: 1.
2.
3.
4.
MIC
R
I
S
S
S
S
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
R
R
R
I
S
S
S
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS STREPTOCOCCI
R
I
S
S
S
S
R
I
S
S
S
S
>
R
R
4
I
I
2
S
S
S
1
S
S
S
S. pneumoniae and streptococci (Group A, B, C and G) therapies based on EUCAST V3.1.
Viridans streptococci therapy based on CLSI M100-S22.
Linezolid (Lzd)
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS STREPTOCOCCI
>
4
2
S
S
S
1
S
S
S
0.5
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. The CLSI interpretative guideline with S. pneumoniae, beta-hemolytic streptococci and viridans streptococci
is 2 for susceptible. Because intermediate and resistant interpretations have not been defined, no
interpretations will be provided if the result is >2.
9020-7493B
NOTE: 1.
2.
3.
4.
5.
6.
6.
4.
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
MIC
S. PNEUMONIAE
(Meningitis)
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
8
R
R
4
R
R
2
R
S
1
I
S
0.5
N/R
S
Therapy based on EUCAST V3.1.
Meropenem (Mer)
NOTE: 1.
2.
3.
S. PNEUMONIAE
(Meningitis)
>
R
R
2
R
S
1
I
S
0.5
I
S
S
0.25
S
S
S
S. pneumoniae (meningitis) and viridans streptococci therapies based on EUCAST V3.1.
Beta-hemolytic streptococci therapy based on CLSI M100-S22.
Meropenem (Mer)
NOTE: 1.
2.
3.
4.
5.
MIC
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
4
R
2
R
1
R
0.5
I
S
S
0.25
S
S
S
0.12
S
S
S
0.06
S
S
S
Therapy based on CLSI M100-S22.
Only systemic therapy will be reported.
The CLSI interpretative guideline for Meropenem with beta-hemolytic streptococci and viridans
streptococci is 0.5 for susceptible. Because intermediate and resistant interpretations have not been
defined, no interpretations will be provided if the result is >0.5.
Results of testing Meropenem should be routinely reported for CSF isolates of S. pneumoniae.
9020-7493B
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
2
R
R
1
I
I
0.5
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
S. PNEUMONIAE
>
R
2
R
1
R
0.5
S
0.25
S
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
S. PNEUMONIAE
>
4
2
1
0.5
0.25
NOTE: 1. Therapy based on CLSI M100-S22.
Penicillin (P)
NOTE: 1.
2.
3.
4.
5.
9020-7493B
MIC
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
R
R
I
S
S
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
R
R
I
S
S
S
S. PNEUMONIAE
(meningitis)
>
R
R
R
16
R
R
R
8
R
R
R
4
R
R
R
2
R
R
I
1
R
R
I
0.5
R
R
I
0.25
R
S
S
0.12
R
S
S
0.06
S
S
S
0.03
S
S
S
Therapy based on EUCAST V3.1.
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
R
8
R
R
4
R
R
2
R
I
1
R
I
0.5
R
I
0.25
R
I
0.12
R
S
S
0.06
S
S
S
0.03
S
S
S
Therapy based on CLSI M100-S22.
The CLSI interpretive guideline for Penicillin with beta-hemolytic streptococci is 0.12 for susceptible.
Because intermediate and resistant interpretations have not been defined no interpretations will be
provided if the result is >0.12.
Results of testing Penicillin should be routinely reported for CSF isolates of S. pneumoniae.
For S. pneumoniae, Penicillin breakpoints are based on isolates from CSF (meningitis). For all other
S. pneumoniae isolates report both meningitis breakpoints (S0.06, R0.12) and non-meningitis breakpoints
(S2, I=4, R8). Breakpoints for oral administration are S0.06, I=0.12-1, R2.
Pristinamycin (Prs)
MIC
S. PNEUMONIAE
STREPTOCOCCI
>
R
R
2
R
I
1
S
S
NOTE: 1. Therapy based on SFM 2012.
NOTE: 1.
2.
3.
4.
MIC
S. PNEUMONIAE
STREPTOCOCCI
>
R
R
4
R
R
2
N/R
N/R
Therapy based on SFM 2012.
Rifampin (Rif)
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
16
8
4
2
1
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
>
R
2
I
1
S
0.5
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. Use for MICroSTREP plus 3, MICroSTREP plus 6C and MICroSTREP plus 6E panels.
Tetracycline (Te)
MIC
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
ViIRIDANS
STREPTOCOCCI
>
R
R
R
4
R
R
I
2
I
I
S
1
S
S
S
NOTE: 1. S. pneumoniae and streptococci (Group A, B, C and G) therapies based on EUCAST V3.1.
2. Viridans streptococci therapy based on CLSI M100-S22.
MIC
S. PNEUMONIAE
>
R
8
R
4
R
2
I
1
S
0.5
S
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
S. PNEUMONIAE
MIC
VIRIDANS
STREPTOCOCCI
R
R
R
I
S
S
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
I
S
S
S
R
I
S
S
S
R
I
S
S
S
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
>
4
2
1
0.5
NOTE: 1. Therapy based on CLSI M100-S22.
TrimethoprimSulfamethoxazole (T/S)
STREPTOCOCCI
(Group A, B, C and G)
VIRIDANS
STREPTOCOCCI
>
R
R
8/152
R
R
4/76
R
R
2/38
I
I
1/19
S
S
0.5/9.5
S
S
0.25/4.75
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
9020-7493B
MIC
Vancomycin (Va)
MIC
S. PNEUMONIAE
>
2/38
1/19
0.5/9.5
0.25/4.75
NOTE: 1. Therapy based on CLSI M100-S22.
BETA-HEMOLYTIC
STREPTOCOCCI
R
I
I
S
S
S. PNEUMONIAE
STREPTOCOCCI
(Group A, B, C and G)
>
R
R
8
R
R
4
R
R
2
S
S
1
S
S
0.5
S
S
0.25
S
S
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
VIRIDANS
STREPTOCOCCI
S. PNEUMONIAE
BETA-HEMOLYTIC
STREPTOCOCCI
VIRIDANS
STREPTOCOCCI
R
R
R
S
S
S
S
VIRIDANS
STREPTOCOCCI
>
8
4
2
1
S
S
S
0.5
S
S
S
0.25
S
S
S
0.12
S
S
S
NOTE: 1. Therapy based on CLSI M100-S22.
2. The CLSI interpretative guideline for Vancomycin with streptococci is 1 for susceptible. Because
intermediate and resistant interpretations have not been defined for streptococci, no interpretations will
be provided if the result is >1.
3. Results of testing Vancomycin should be routinely reported for CSF isolates of S. pneumoniae.
9020-7493B
MIC
>
16
8
4
2
1
0.5
0.25
0.12
0.06
0.03
NOTE: 1. Therapy based on EUCAST V3.1.
NOTE: 1.
2.
3.
4.
MIC
HAEMOPHILUS
R
R
R
R
R
S
S
S
S
S
S
HAEMOPHILUS
>
R
8
R
4
R
2
I
1
S
0.5
S
0.25
S
0.12
S
0.06
S
0.03
S
Therapy based on CLSI M100-S22.
MIC
>
4/2
2/1
1/0.5
0.5/0.25
0.25/0.12
NOTE: 1. Therapy based on CLSI M100-S22.
9020-7493B
HAEMOPHILUS
R
S
S
S
S
S
NOTE: 1.
2.
3.
4.
MIC
HAEMOPHILUS
>
4
S
2
S
1
S
0.5
S
0.25
S
Therapy based on CLSI M100-S22.
Cefaclor (Cfr)
MIC
>
16
8
2
1
NOTE: 1. Therapy based on CLSI M100-S22.
MIC
HAEMOPHILUS
R
I
S
S
S
HAEMOPHILUS
>
2
S
1
S
0.5
S
0.25
S
0.12
S
NOTE: 1. Therapy based on CLSI M100-S22.
9020-7493B
NOTE: 1.
2.
3.
4.
4.
HAEMOPHILUS
>
32
16
8
4
2
S
1
S
0.5
S
0.25
S
0.12
S
0.06
S
0.03
S
Therapy based on CLSI M100-S22.
Ceftriaxone (Cax)
NOTE: 1.
2.
3.
MIC
MIC
HAEMOPHILUS
>
8
4
2
S
1
S
0.5
S
0.25
S
0.12
S
Therapy based on CLSI M100-S22.
Cefuroxime (Crm)
MIC
>
4
2
1
0.5
NOTE: 1. Therapy based on CLSI M100-S22.
9020-7493B
HAEMOPHILUS
R
S
S
S
S
MIC
>
8
4
2
1
0.5
0.25
NOTE: 1. Therapy based on CLSI M100-S22.
MIC
>
16
8
4
2
NOTE: 1. Therapy based on EUCAST V3.1.
NOTE: 1.
2.
3.
4.
MIC
HAEMOPHILUS
R
I
S
S
S
S
S
HAEMOPHILUS
R
R
R
R
S
HAEMOPHILUS
>
R
8
R
4
I
2
S
1
S
Therapy based on CLSI M100-S22.
Ciprofloxacin (Cp)
MIC
>
4
2
1
0.5
0.25
NOTE: 1. Therapy based on EUCAST V3.1.
9020-7493B
HAEMOPHILUS
R
R
R
R
S
S
MIC
HAEMOPHILUS
>
2
1
S
0.5
S
0.25
S
0.12
S
0.06
S
NOTE: 1. Therapy based on CLSI M100-S22.
Clindamycin (Cd)
MIC
HAEMOPHILUS
>
4
2
1
0.5
NOTE:
MIC
HAEMOPHILUS
>
2
1
0.5
0.25
Erythromycin (E)
MIC
HAEMOPHILUS
>
4
2
1
0.5
9020-7493B
NOTE:
MIC
HAEMOPHILUS
>
4
2
1
0.5
0.25
Levofloxacin (Lvx)
MIC
>
8
4
2
1
0.5
0.25
NOTE: 1. Therapy based on EUCAST V3.1.
NOTE: 1.
2.
3.
4.
5.
MIC
HAEMOPHILUS
R
R
R
R
S
S
S
HAEMOPHILUS
>
R
8
R
4
R
2
R
1
I
0.5
N/R
Therapy based on EUCAST V3.1.
Meropenem (Mer)
NOTE: 1.
2.
3.
4.
5.
9020-7493B
MIC
HAEMOPHILUS
>
4
2
1
0.5
S
0.25
S
0.12
S
0.06
S
Therapy based on CLSI M100-S22.
MIC
HAEMOPHILUS
>
16
8
4
2
1
0.5
0.25
0.12
0.06
0.03
NOTE: 1. Use for MICroSTREP plus 5 and MICroSTREP plus 3 panels only.
Pristinamycin (Prs)
MIC
HAEMOPHILUS
>
4
2
MIC
>
16
8
4
2
1
0.5
NOTE: 1. Therapy based on CLSI M100-S22.
MIC
>
8
4
2
1
0.5
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
>
4
2
1
NOTE: 1. Therapy based on CLSI M100-S22.
HAEMOPHILUS
R
R
R
R
I
S
S
HAEMOPHILUS
R
R
R
I
S
S
HAEMOPHILUS
R
I
S
S
MIC
>
8/152
4/76
2/38
1/19
0.5/9.5
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
Vancomycin (Va)
MIC
>
2/38
1/19
0.5/9.5
0.25/4.75
NOTE: 1. Therapy based on CLSI M100-S22.
HAEMOPHILUS
R
R
R
R
I
S
HAEMOPHILUS
R
I
I
S
S
HAEMOPHILUS
>
8
4
2
1
NOTE: 1. Therapy based on EUCAST V3.1.
MIC
HAEMOPHILUS
>
8
4
2
1
0.5
NOTE: 1. Therapy based on CLSI M100-S22.
9020-7493B
9020-7493B
ENTEROBACTER GROUP
Enterobacter aerogenes
Pantoea agglomerans
Enterobacter amnigenus 1
Enterobacter amnigenus 2
Enterobacter asburiae
Enterobacter cancerogenous
Enterobacter cloacae
Enterobacter gergoviae
Enterobacter hormaechei
Enterobacter intermedius
Enterobacter sakazakii
Enterobacter species
Enterobacter taylorae
ESBL GROUP- SCREENING
Escherichia coli
Escherichia coli LYS-/ORNEscherichia coli O157:H7
Klebsiella oxytoca
Klebsiella pneumoniae/oxytoca
Klebsiella pneumoniae
Proteus mirabilis
ESBL GROUP- CONFIRMATION
Citrobacter amalonaticus
Citrobacter koseri
Citrobacter farmeri
Citrobacter koseri
Citrobacter species
Enterobacter aerogenes
Enterobacter cloacae
Escherichia coli
Escherichia coli LYS-/ORNKlebsiella oxytoca
Klebsiella pneumoniae/oxytoca
Klebsiella pneumoniae
Morganella morganii
Proteus mirabilis
Proteus vulgaris
Providencia rettgeri
Salmonella species
Serratia marcescens
PROTEUS/PROVIDENCIA GROUP
Proteus penneri
Proteus species
Proteus vulgaris
Proteus vulgaris/penneri
Providencia alcalifaciens 1-2
Providencia alcalifaciens/rustigianii
Providencia rettgeri
Providencia rustigianii
Providencia species
Providencia stuartii
9020-7493B
Moraxella non-liquefaciens
Moraxella osloensis
Psychrobacter (M.) phenypyruvicus
Moraxella species/Psychrobacter longate
Neisseria elongata subsp. nitroducans
Ochrobactrum anthropi
Oligella species
Oligella urethralis
Pasteurella aerogenes
Mannheimia (P.) haemolytica
P. pneumoniae/A. urea/M. haemolytica
Pasteurella multocida
Pasteurella pneumotropica
Pasteurella species
Actinobacillus (P.) ureae
Photorhabdus luminescens
Plesiomonas shigelloides
Pseudomonas alcaligenes
Pseudomonas alcaligenes/pseudoalcaligenes
Pseudomonas fluorescens
Pseudomonas fluorescens/putida
Pseudomonas (C.) luteola
Pseudomonas mendocina
Pseudomonas (F.) oryzihabitans
Pseudomonas pseudoalcaligenes
Pseudomonas putida
Pseudomonas species
Pseudomonas stutzeri
Pseudomonas stutzeri/mendocina
Ralstonia (B.) pickettii
Roseomonas species
Shewanella putrefaciens
Sphingomonas (P.) paucimobilis
Stenotrophomonas (X.) maltophilia
Tatumella ptyseos
Vibrio alginolyticus
Vibrio hollisae
Vibrio cholerae
Vibrio damsela
Vibrio fluvialis
Vibrio fluvialis/furnissii
Vibrio furnissii
Vibrio metschnikovii
Vibrio mimicus
Vibrio parahaemolyticus
Vibrio species
Vibrio vulnificus
Yersinia enterocolitica group
Yersinia frederiksenii
Yersinia intermedia
Yersinia kristensenii
Yersinia pestis
Yersinia pseudotuberculosis
Yersinia ruckeri
Yersinia species
Yokenella regensburgei
Page 155 of 158
9020-7493B
9020-7493B
9020-7493B