Вы находитесь на странице: 1из 19

CSF and Ventricular System

CSF is a colorless, clear fluid


produced by choroid plexus in
third and fourth ventricles.
500-600 ml CSF produced daily
125-150 ml circulates in the
ventricular
system and subarachnoid space
at one time
(remainder is reabsorbed)
Indications for Measuring ICP

TBI with GCS of less than or


Fulminant hepatic failure
equal to 8
with encephalopathy
with an abnormal CT scan
results Ischemic Stroke with

Normal CT scan results with massive edema


hypotension, posturing, and Meninigitis
older than 40.
Cysts
ICH
Hydrocephalus
SAH
Congenital anomalies
Cerebral Edema
Craniosynostisis
Mass
External Ventricular Drainage
(EVD)
External Ventricular Drainage (EVD) is a
treatment that allows the temporary
drainage of Cerebrospinal Fluid (CSF)
from the ventricles of the brain, relieving
raised intracranial pressure.
Continuous EVD
Close EVD
Complications
Complications arising from EVD include hemorrhage,
misplacement, dislodgement, disconnection, blockage, and,
most significantly, infection.

EVD-related infections may lead to further serious


complications such as ventriculitis, meningitis, cerebritis,
brain abscess and subdural empyema.

These complications can cause profound neurological


damages, significant morbidities and mortalities.
Complications
EVD-related infections require immediate and
prolonged treatment once detected.

Empirical antibiotics with good CSF penetration


should be given to cover the common offending
organisms.

The commonly used agents are cephalosporins and


rifampicin.

Intraventricular vancomycin may be used for


resistant organisms.
Bacteriology
Coagulase-negative Staphylococcus most common bacteria
isolated in patients with EVD-related infections, accounting for up to
47% of infected cases
Other common organisms : Enterococcus, Enterobacter and
Staphylococcus aureus.
This pattern coincides with that of the usual skin flora and hospital
environment although the bacteriology may also be influenced by
the presence of different nosocomial microorganisms in different
institutions.
Gram-positive organisms are classically associated with ventriculitis
Ventriculitis associated with EVD were not uncommonly caused by
gram-negative bacteria such as Klebsiella.
This is postulated to be a nosocomial colonization caused by
prolonged hospital stay and the selection pressure from
prophylactic antibiotics targeting gram-positive organisms
Mechanisms of Infection
The presence of an EVD essentially externalizes the intra-
cranial cavity and ventricular system, and is a potential route
for retrograde infection.
The ventricular catheter as an indwelling foreign body is
prone to bacterial colonization that may result from other
unrelated sources such as systemic bacteremia.
EVD-related infections may arise from either inoculation of
skin flora during insertion, and/or contamination and
colonization of the drainage system during the post-operative
period, with subsequent retrograde infections
The risk of inoculation is related to the sterility of the insertion
procedure

It may increase with repeated revisions due to elective


replacement or other clinical indications.
The risk of colonization and contamination is affected by the
manipulation of the drainage system, EVD maintenance
protocol, and the technique of insertion.
Risk Factors
A. Subarachnoid hemorrhage (SAH)
and Intraventricular hemorrhage
(IVH)

Significant higher incidence of EVD-


related infections in patients with SAH
or IVH when compared with patients
with non-hemorrhagic pathologies
B. Craniotomy and other
neurosurgical procedures
The infection rate in group of
patients whom also had undergone
neurosurgical procedures was 15.2%,
compared with 7.8% in the EVD-only
group
D. Duration of drainage
The risk of infection would increase
with prolonged EVD
Current evidence : routine revision of
EVD in the absence of other clinical
indications is not recommended.
E. Manipulation of the EVD system
Manipulations and opening of the otherwise closed
EVD system for CSF sampling or flushing may
introduce microorganisms and potentially cause
infection.
Historically, CSF was sampled routinely and indeed
daily in an attempt to pick up early infections
increase the risk of infection
Decreasing the frequency of CSF sampling to once
every 3 days lower incidence of ventriculitis
CSF sampling should be performed when there is
clinical suspicion of infection
F. Prophylactic antibiotics
The use of prophylactic antibiotics
was found to significantly reduce the
risk of EVD- related infections
Prolonged use of ampicillin/sulbactam
and aztreonam resulted in a lower
infection rate compared with a single
dose of perioperative
ampicillin/sulbactam.
Prophylactic intraventricular
antibiotics possible beneficial
effect
Prophylactic intraventricular
vancomycin and gentamicin together
with systemic antibiotics significantly
decreased the risk of infection in
shunted patients.
G. Coated ventricular catheter
Coating the surface of the catheter
with special materials or antibiotics
may decrease bacterial colonization
and thus prevent infection.
Insertion of EVD
Performed in the operating theatre whenever
possible, with a minimal number of attending staff
Performed in a dedicated clean treatment room if the
prosedure has to be done outside the operating
theatre, with a surgeon and the asisting nurse
dressed in sterile gown and gloves after proper hand
hygiene measures
Prophylactic antibiotics to cover skin flora before
incision
Shampoo the entire scalp with betadine, and
disinfect with iodine alcohol
Covering the wound with sterile dressing
Maintenance EVD
Respecting the close system as far as
possible
Avoid CSF sampling unless infection
is clinically suspected
Disinfect the connector and adopt
strict aseptic technique if any breach
of the system is needed
No routine EVD revision
Conclusion

Infection is a major and serious complication of EVD that


may cause significant morbidities and even mortalities.
Several risk factors of EVD-related infections have been
identified and preventive measures aimed at reducing
these factors have been developed.
These include the use of prophylactic systemic
antibiotics, antibiotics-coated catheters and
subcutaneous catheter tunnelling.
Adopting a clearly defined protocol which addresses
various aspects of insertion and maintenance
minimize the occurrence of EVD-related infections.