Ventriculitis

OVERVIEW

Bacterial ventriculitis (BV) is inflammation of the ventricular drainage system, usually due to bacterial infection of the cerebrospinal fluid (CSF)

  • Ventriculitis can occur as a primary process, or as a complication of:
    • meningitis (30% of adult cases and up to 90% of neonatal cases)
    • cerebral abscess
    • intraventricular haemorrhage, or
    • iatrogenesis
  • Frequently associated with the presence of a CSF shunt, external ventricular drainage (EVD), or other intracranial device
  • most CSF shunt-related infections occur in the first month after insertion

EVD-RELATED VENTRICULITIS

Bacteria can access through skin site and connections between tubes

  • EVD-related infections rates range from <1% to 40% (9% in the UK according to Jamjoon et al, 2017)
  • mortality rates vary from 10% to 75%

Risk factors

  • length of time the EVD is in place (e.g >7 days)
  • management (e.g. frequency of manipulation of EVD, especially repeated sampling)
  • type of EVD
  • insertion technique
  • multiple catheter insertions or exchanges
  • underlying disease
  • neurosurgery
  • CSF leakage
  • previous infections

CAUSE

Usual organisms in EVD and CSF shunt infections:

  • Staphylococcus aureus
  • Coagulase negative Staphylococci (S. epidermidis)
  • GNBs (up to 25%; more common if VP shunt due to peritoneal contamination): Escherichia coli, Klebsiella species, Acinetobacter, and Pseudomonas species
  • consider fungi if immunosuppressed

CLINICAL FEATURES

Clinical features may be subtle in EVD-associated infections

  • headache
  • nausea and vomiting
  • fever
  • altered mental state
  • focal neurological deficits
  • secondary hydrocephalus/ raised ICP

INVESTIGATIONS

Blood tests

  • WBC, CRP and procalcitonin are not very helpful

CSF analysis

  • high WCC in the CSF (Normal RCC:WCC Ratio = 500:1 but this alone is of questionable reliability)
  • CSF protein may be normal or high
  • Reduction in CSF glucose may be a more sensitive indicator of infection
  • Elevated CSF lactate has not been proven of utility
  • Cell index (ratio of leukocytes to erythrocytes in CSF divided by leukocytes to erythrocytes in peripheral blood) may prove to be useful
    • usually about 1
    • tends to increase in ventriculitis, and fall with response to antibiotics
    • Beer et al (2009) used a 5-fold increase in Cell Index as indicative of ventriculitis (should be considered experimental)

CT/ MRI

  • Ventriculitis is detected best by T2 fluid-attenuated inversion recovery (FLAIR) images showing periventricular hyperintensity on ependymal enhancement and irregular intraventricular debris
  • CT may be non-specific

DIAGNOSTIC PITFALLS

In post-neurosurgical patients or patients with a ventriculostomy:

  • systemic inflammatory response and clinical signs may be absent or subtle
  • the CSF cell count may be elevated as a result of surgical manipulation and inflammation
  • no single parameter can reliably predict or exclude EVD-related infection
  • imaging should not delay treatment

MANAGEMENT

Treatment

  • Clinical suspicion of nosocomial ventriculitis mandates prompt initiation of empiric antibiotic therapy
  • Intravenous antibiotics (may vary according to local guidelines):
    • vancomycin 1.5 g (<12y: 30 mg/kg up to 1.5 g) Q12H (adjust for renal function)
    • PLUS EITHER:
      • ceftazidime 2 g (child: 50 mg/kg up to 2 g) IV Q8H, OR
      • meropenem 2 g (child: 40 mg/kg up to 2 g) Q8H
  • Intraventricular antibiotics
    • not used routinely
    • use preservative-free formulations
    • options (may vary according to local guidelines):
      • vancomycin 10 to 20 mg daily
      • gentamicin 4 to 8 mg daily, or
      • amikacin 30 mg daily
  • Removal +/- replacement of infected EVD if present
    • this may not be necessary unless there is inadequate response to antimicrobial therapy or the CSF is purulent
  • rationalise antibiotics according to sensitivity
  • antibiotic duration is usually 14 days after the last positive culture

Prevention in ICU

  • antibiotic- and silver-impregnated EVD catheters appear to reduce rates of BV but are not in universal use
  • remove EVD as early as possible (review indication daily)
  • access EVD in a protocolised meticulous sterile fashion
  • minimise the frequency of EVD manipulations
  • routine CSF cultures are not necessary but should be performed if fever (e.g. >38.5 C), peripheral leukocytosis, neurological deterioration, or a change in CSF appearance is noted

References and Links

Journal articles

  • Beer R, Pfausler B, Schmutzhard E, et al. Management of nosocomial external ventricular drain-related ventriculomeningitis. Neurocrit Care. 2009;10(3):363-7 [PMID 18982457]
  • Flint AC, Rao VA, Renda NC, et al. A simple protocol to prevent external ventricular drain infections. Neurosurgery. 2013 Jun;72(6):993-9; discussion 999 [PMID 23467249]
  • Jamjoom AAB, Joannides AJ, Poon MT, et al. Prospective, multicentre study of external ventricular drainage-related infections in the UK and Ireland. Journal of neurology, neurosurgery, and psychiatry. 2017 [PMID 29070645]

FOAM and web resources


CCC 700 6

Critical Care

Compendium

Chris is an Intensivist and ECMO specialist at The Alfred ICU, where he is Deputy Director (Education). He is a Clinical Adjunct Associate Professor at Monash University, the Lead for the  Clinician Educator Incubator programme, and a CICM First Part Examiner.

He is an internationally recognised Clinician Educator with a passion for helping clinicians learn and for improving the clinical performance of individuals and collectives. He was one of the founders of the FOAM movement (Free Open-Access Medical education) has been recognised for his contributions to education with awards from ANZICS, ANZAHPE, and ACEM.

His one great achievement is being the father of three amazing children.

On Bluesky, he is @precordialthump.bsky.social and on the site that Elon has screwed up, he is @precordialthump.

| INTENSIVE | RAGE | Resuscitology | SMACC

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