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I. DEFINITION:
Accesses are devices used as a life line for the acute and chronic renal failure patient
for the dialysis. It must be patent and functioning at all times, so proper Heparinization
of the permicath is necessary to prevent clotting of the access.
II. PURPOSES:
1. To achieve successful prescribed Hemodialysis treatment.
2. To keep the patient access functioning properly
3. To provide guideline for the nurses how to change the clotted blood lines and
dialyzer during dialysis treatment.
4. To establish procedures for declotting vascular access devices for adult patients
using tissue plasminogen activator (t-PA).
5. To assess the arterial blood line for cracks or defects that may cause the
introduction of air into the blood circuit or the loss of blood
6. To safety and quickly replace a defective arterial blood line during Hemodialysis
with minimal blood loss.
V. REFERENCES:
VI. ATTACHMENTS:
VII. DISTRIBUTIONS:
1. Hemodialysis Unit
2. Central Nursing Office
Equipment/Supplies:
1. Sterile water for injection
2. Tissue Plasminogen Activator (t-PA)
3. Two syringes (10ml)
4. Alcohol swabs
A. The following reactions have been associated with t-PA in doses recommended for lysis of
pulmonary embolism. Possible adverse reactions include:
• Bleeding
• Allergies (Bronchospasm, skin rash, and fever)
• Anaphylaxis
• Nausea and vomiting, fever and chills, shaking chills (rigors), transient hypotension or
hypertension, dyspea, tachycardia, cyanosis, back pain, hypoxemia, acidosis.
Patient/Family Education:
The patient and family/significant other(s) should be educated at their level of understanding of the
following:
a) The purpose of t-PA.
b) Potential adverse reactions of t-PA.
Documentation:
a) When using t-PA, document verification of occlusion, volume of t-PA instilled, number of
attempts required, result of instillation, and patient response in the medical record. Document
dosage of t-PA on Medication Administration Record (MAR) Outpatient Assessment Form.
b) Any adversity caused by t-PA should promptly be reported as an adverse drug.
c) Document patient/family education in the Patient Family Education Form.
ATTACHMENT - A
NSP/HM - 039.14
ALMANA GENERAL HOSPITAL – HEMODIALYSIS UNIT AL AHSA
GUIDELINES FOR THE USE OF ALTEPLASE FOR THE OCCLUDED
HEMODIALYSIS CATHETERS
A well functioning vascular access is a prerequisite for Hemodialysis (HD). To be consistent with
national and international standards, the preferred form of HD vascular access as the native arterio
venous fistula (AVF), followed by the artificial Arteriovenous graft (AVG) and lastly the central
venous catheter (CVC).
Despite all best efforts for patients undergoing HD to have an AVF (preferred) or AVG (2nd choice),
there will always be patients that receive HD by CVC on a temporary or permanent basis. The most
common complications of the CVC are thrombosis and infection (Develter, 2005 and Little, 2001).
Even with care, fewer than half the catheters placed as “long-term accesses” are in use a year after
placement (Ponikvar, 2005)and about a third are remove d because they fail to deliver adequate blood
flow (K/DOQI 2006)
The initial approach for the treatment of a dysfunctional or blocked catheter is conservative – rule out
mechanical issues such as machine problems or kinks in the catheter and forcefully flush the lines with
normal saline. If conservative measures fail, the administration of thrombolytic agents may be
required.
If CVC dysfunction is identified, rule out causes other than thrombosis as the source of the
dysfunction.
Causes of CVC dysfunction other than thrombosis is included mechanical reasons, kinks, misplaced
sutures, catheter migration, drug precipitation, hypovolemia, patient position, catheter integrity, holes
and cracks (KDOQI;2006)such causes need to be ruled out prior to the use of thrombolytics.
Alteplase is the thrombolytic agent of choice for treating occlude HD CVCs. Alteplase works by
binding to fibrin in a thrombus, then converting the entrapped plasminogen to plasmin which results in
local fibrinolysis (i.e. digests fibrin and dissolves blood clot).
While Alteplase has proven to be useful in the management of catheter related thrombotic occlusion.
Selection of method will depend on individual circumstances including the severity of the occlusion
and the timing and urgency of the need for dialysis.
Chronic use of Alteplase is strongly discouraged other than in exceptional circumstances (i.e., resistant
CVCs and :
CVC is the last option for HD access AND the patient is unable to tolerate further CVC replacements;
ORA maturing AVF or AVG is imminent.
IF NO FLOW OR BLOOD PUMP SPEED IS LESS THAN 200 ML/MIN
PUSH / PAUSE METHOD:
• Instill Alteplase 1mg per mL into each catheter lumen then add NS 0.9% without preservative to fill the
internal volume of each lumen plus 0.1mL overfill
• Attach syringe filled with NS 0.9% to each lumen. Wait 10 minutes, then gently push NS 0.9% 0.3 mL
into each lumen. Wait another 10 minutes, and then repeat NS 0.9% 0.3 mL push. Wait another 10
minutes, than aspirate clots using a 10 mL syringe and discard. May push remaining Alteplase if unable
to withdraw. Forcefully flush each catheter lumen.
SHORT DWELL METHOD:
• Instill Alteplase 1mg per mL into each lumen then add NS0.9% without preservative to fill the internal
volume of each lumen plus 0.1 mL overfill.
• Leave Alteplase solution in situ for 60 minutes, then withdraw the solution and clot(s); May push
remaining if unable to withdraw. Forcefully flush each catheter lumen.
OVERNIGHT DWELL METHOD:
• Instill Alteplase 1mg per mL into each catheter lumen then add NS 0.9% without preservative to fill the
internal volume of each lumen plus 0.1mL overfill
• Leave Alteplase solution in situ until next Hemodialysis treatment. Prior to start of next treatment,
withdraw the solution and clot(s); May push remaining if unable to withdraw. Forcefully flush each
catheter lumen.
ATTACHMENT – B
NSP / HM – 039.14
ALMANA GENERAL HOSPITAL – HEMODIALYSIS UNIT‐ AL AHSA
ALGORITHM FOR THE USE OF ALTEPLASE IN OCCLUDED HD CVCs
Difficulty instilling or aspirating catheter lumens, blood pump speed < 250ml/min or decrease in blood flow of 20% during HD
↓
• Rule out machine problems
• Check for kinks beneath catheter clamps or at exit site
• Change patient position
• Confirm the HD catheter has not been used for non‐HD uses (e.g. TPN)
• Flush lines forcefully with 20 ml NS into each lumen
• Reverse lumens & increase BPS as high as possible
• If a maturing peripheral access, is it ready to be cannulated?
• If catheter inserted < 1 week, obtain order for CXR to rule out catheter position problem
↓
Adequate flow? → Yes → Adequate blood flow established; proceed with HD; continue to observe & monitor;
lock catheter with heparin
↓
NO
↓
As per physician orders, instill Alteplase using one of the following methods:
1. If no flow or blood pump speed < 200 ml/min, instill 1‐2mg/ lumen using:
a. Push / pause method; or
b. Short dwell method (60 minutes); or
c. Long dwell method (over night)
2. If blood pump speed is ≥ 200 ml/ min and ≥ 300 ml / min:
a. Instill 1‐2mg / lumen using the long dwell method (overnight)
↓
YES Adequate Flow?
↓ No
Repeat instillation of Alteplase using one of the
↓ No
YES
Adequate Flow?
NO
↓
Contact treating physician to investigate and INTERVENE:
• Chest X‐ray PA & Lateral
• CVC Exchange
• Creation of AVF or AVG (if feasible)
Under the exceptional circumstances,
Adequate Flow?
↓ YES YES NO
Treating physician may consider
implementing the protocol for
↓
YES resistant CVC (Alteplase to cap off
↓ CVC post‐ dialysis 1‐3 x/wk
Adequate blood flow is established; proceed with HD; continue
to observe & monitor; lock catheter with heparin
ATTACHMENT – C
NSP / HM – 039.14