Investigation of a cluster of ventriculostomy associated gram-negative bacillary meningitis cases in a neurosurgical intensive care unit.

Kennedy C, McNeely D, Houston T, Wallace C, McCarthy MK, Conly J.

APIC 1997 Conference, New Orleans, June 8-12, 1997 (poster presentation)

ABSTRACT

Although postoperative infections of cerebrospinal fluid (CSF) associated with external ventriculostomy drainage systems occur with a frequency of approximately 10% and are not infrequently caused by gram-negative bacilli (GNB), there have been few reported clusters. During a 3 month period, June-Sept 1996, 9 patients were identified with meningitis in the early postoperative period. Of these patients, 8 were in the neurosurgical intensive care unit, with 1 in a medical intensive care unit. Six had GNB identified from ventriculostomy samples, as a single isolate in 3 and polymicrobial in 3 other cases. A total of 23 different isolates were identified with 8 (35%) identified as either Klebsiella-Enterobacter or Pseudomonas. The remainder of the isolates were staphylococci or streptococci. The Enterobacter isolates had dissimilar antibiograms. All patients had an external ventriculostomy drainage system in place. Potential risk factors identified included concomitant GNB endotracheal colonization, tracheostomy and ventriculostomy procedures performed on the same day, multiple and/or bedside ventriculostomy tubing changes, embolization or coiling procedures performed, and a leaking ventriculostomy site. The isolation of dissimilar strains between these patients and the colonization at other body sites did not support a common source outbreak. Recommendations made included the adherence to strict aseptic technique including a review of sampling procedures, the use of sterile gloves during calibration of the line, discontinuation of the practice of bedside tubing changes, consistent use of a closed endotracheal suctioning system, increased use of the Camino drainage system and ventriculostomy changes to be done prior to tracheotomy procedures. In the following 6 months, there has been only one episode of ventriculostomy associated GNB meningitis.

METHODS

Description of the Cluster:

Venticulostomy Infection Episodes 1996


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CLINICAL and MICROBIOLOGIC INVESTIGATIONS


RESULTS
MICROBIOLOGIC


INTRODUCTION

  • External intracranial pressure (ICP) monitoring systems consist of a
    catheter or screw (bolt), sensor, pressure tubing, transducer and a recording device. They are used in the management of cerebral hypertension after a neurological episode.

      Point of Practice Observations:
    1. Sterile gloves were not consistently used when calibrating or obtaining CSF from the system
    2. Ventriculostomy catheters were changed q6-7 days
    3. A few ventriculostomy changes had been done in the ICU
    4. Sampling was done from both the proximal and distal ports
    5. A tracheostomy was done prior to a ventriculostomy change in the OR
    6. The system was entered daily for the routine collection of CSF for culturing
    7. In-line suction catheters were not used consistently

      SUMMARY and CONCLUSIONS
      • Only 2 ventriculostomy associated infections were identified during the next 6 mos (1 associated with GNB)
      • Implementation of the recommendations appeared to be associated with a significant decrease in ventriculitis
      • It is uncertain which of the recommendations was responsible for the reduction but those directed towards reducing cross-contamination between ETT secretions and the ventriculostomy system appear to be significant
      • Surveillance of ICP system infections continues and documentation of bedside insertions has been implemented

      RISK FACTORS FOR INFECTION
      • intracranial hemorrhage, open head injury,
      • CSF leak, craniotomy
      • manipulation, replacement or irrigation of the system
      • concurrent systemic infections e.g. pneumonia
      • insertion technique (risk- tunneling catheter)
      • insertion location (OR, ER or ICU)
      • duration of monitoring and catheter days
      • ? catheter care (dressing or stopcocks)
      • ? prophylactic antibiotic or steroid use

      OBSERVATIONS
      • 9- ICP drainage
      • 3- ICU bedside changes
      • 3- ventriculostomy/tracheotomy procedures
      • 2- intra-thecal therapy
      • 3- embolization
      • 1- implant (Omaya)
      • 1- acute cholecystitis post-op

      RECOMMENDATIONS

      • Aseptic technique and sterile gloves to be used while manipulating an ICP system
      • In-line suction catheters to be used
      • Assess necessity of routine changes of ventriculostomy catheter and sets
      • It is preferable to change ventriculostomy catheters in the OR
      • Ventriculostomy changes should precede a tracheotomy
      • A closed monitoring system should be used if drainage is not required
      • CSF samples should be collected from a port rather than a stopcock.
      • CSF samples should be collected from a distal rather than proximal port
      • The need for routine daily CSF sampling should be reviewed.
      • Policies should indicate the person responsible for obtaining CSF specimens

      MICROBIOLOGY

      Patient 1

        June 13 ventriculostomy
        June 14 embolization, CSF: Klebsiella pneumonia, group A haemolytic Streptococcus
        June 15 sputum: Klebsiella pneumonia, group A haemolytic Streptococcus

      Patient 2
        June 18 ventriculostomy
        June 20 CSF Klebsiella pneumonia, Enterobacter cloacae
        June 27 sputum Klebsiella pneumonia

      Patient 3
        June 25 ventriculostomy
        June 27 embolization
        June 30 CSF Streptococcus mitis

      Patient 4
        July 18 ventriculostomy
        July 19 CSF Pseudomonas aeruginosa
        July 13 sputum Pseudomonas aeruginosa

      Patient 5
        June 24 ventriculostomy removed/ VP shunt inserted
        July 7 CSF Staphylococcus aureus
        June 14 sputum Staphylococcus aureus

      Patient 6
        July 19 ventriculostomy and tracheotomy
        July 19 CSF Pseudomonas aeruginosa
        July 22 sputum Pseudomonas aeruginosa

      Patient 7
        July 19 ventriculostomy
        July 20 CSF Klebsiella pneumonia
        July 20 sputum Klebsiella pneumonia

      Patient 8
        August 7 ventriculostomy (bedside)
        August 12 CSF Enterobacter cloacae
        August 15 exit site(leaking) Enterobacter cloacae

      Patient 9
        July 24 Omaya removed, VP shunt
        July 24 CSF Staphylococcus aureus

      REFERENCES
      1. Aucoin PJ et al. Intracranial pressure monitors: epidemiological study of risk factors and infections. Am J Med 1986;80:369-76.
      2. Brader MK et al. Ventriculostomy and intracranial pressure monitoring: in search of a 0% infection rate. Heart & Lung 1995;24:166-72.
      3. Holloway KL et al. Ventriculostomy infections: the effect of monitoring duration and catheter exchange in 584 patients. J Neurosurg 1996;85:419-24.
      4. Paramore CG et al. Relative risks of ventriculostomy infection and morbidity. Acta Neurochir (Wien) 1994;127:79-84.
      5. Hickman KM et al. Intracranial pressure monitoring: review of risk factors associated with infection. Heart & Lung 1990;19:84-91.
      6. Schultz M et al. Bacterial ventriculitis and duration of ventriculostomy catheter insertion. J Neurosci Nurs 1993;25:158-164.
      7. Franges EZ et al. Infections related to intracranial pressure monitoring. J Neurosci Nurs 1988;20:94-103.

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