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

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