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Impact of Ventricular Catheter Used With Antimicrobial Agents on Patients With a Ventricular Catheter

The Impact of Ventricular Catheter Impregnated With Antimicrobial Agents on Infection in Patients With Ventricular Catheter: A Prospective Randomized Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00286104
Enrollment
184
Registered
2006-02-03
Start date
2004-04-30
Completion date
2009-06-30
Last updated
2009-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hydrocephalus, Intracranial Hypertension

Keywords

Ventriculitis, External ventricular catheter, Antibiotic-impregnated

Brief summary

External ventricular catheters are used for intracranial pressure monitoring and temporary cerebrospinal fluid (CSF) drainage in neurosurgery. The incidence of ventriculostomy-related cerebrospinal fluid infections had been quoted as between 2.2% to 10.4% in the more recent literature. Previous prospective studies in the investigators' unit have shown that the use of dual antibiotics prophylaxis in patients with external ventricular drain was associated with decreased incidence of CSF infection but was complicated with opportunistic extracranial infections. The current practice is to cover with prophylactic dual antibiotics unless guided by microbiology results for all patients with external ventricular drain. In recent years, cerebrospinal fluid shunt catheters impregnated with antimicrobial agents have been available. Experimental studies have shown that they provide protection against staphylococcal aureus and coagulase-negative staphylococci strains for between 42 days and 56 days. Theoretically, they provide the antibiotic prophylaxis locally without the associated complications of systemic antibiotics. It is hypothesized that the use of antibiotic-impregnated catheters instead of systemic antibiotic prophylaxis will not increase the rate of cerebrospinal fluid infection, will decrease the rate of opportunistic/nosocomial infections and improves the overall outcome in these patients; that would convert into a reduction in treatment cost of these patients.

Detailed description

Objective: 1. To assess the cranial and extracranial infection rate of systemic antibiotic prophylaxis versus antibiotics-impregnated catheter. 2. To assess the patients' outcome and carry out cost analysis for systemic antibiotic prophylaxis versus antibiotics-impregnated catheter. Design: Prospective randomized controlled trial Hypothesis: The use of antibiotics-impregnated catheter instead of systemic antibiotic prophylaxis will not increase the rate of cerebrospinal fluid infection, will decrease the rate of opportunistic/nosocomial infection and improves the overall outcome in these patients; that would convert into a reduction in treatment cost of these patients. Method: After ventricular catheter insertion, patients will be randomized into one of the two groups: 1. Periprocedural antibiotics: Only ie Unasyn and Rocephin and insertion of the antibiotics-impregnated ventricular catheter. 2. Periprocedural antibiotics and prophylactic dual antibiotics ie Unasyn and Rocephin and insertion of ventricular catheter without impregnation of antibiotics. Primary outcome variable: Cerebrospinal fluid infection and extracranial infection. Sample size: We aim to recruit a total of 180 patients with 90 patients in each arm and expect to complete patient recruitment in 2-3 years. The calculation is based to detect a difference of nosocomial infection rate between 20% and 40%, with 5% level of significance and 80% power. Projected results and significance: The project has a good chance to be the first clinical study to the outcome and cost impacts of antibiotic-impregnated ventricular catheter.

Interventions

DEVICEAntibiotics-impregnated ventricular catheter (Bactiseal®)

Antibiotics-impregnated ventricular catheter (Rifampicin- and Clindamycin-impregnated)

DEVICEPlain ventricular catheter (Codman EDS II/III)

Plain ventricular catheter

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients with external ventricular drain inserted 2. Patients with external ventricular drain in-situ planned for at least 5 days

Exclusion criteria

1. Known CSF infection including meningitis 2. Known sepsis 3. Uncorrected coagulopathy 4. No consent available

Design outcomes

Primary

MeasureTime frame
Cerebrospinal fluid infection rateFirst 30 days
Extracranial infection rateFirst 30 days

Secondary

MeasureTime frame
Mortality rateAt discharge and six months
Glasgow Outcome Scale ExtendedAt discharge and at six months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026