About this trial
The aim of the current study is to evaluate the difference between proximal and distal CSF sampling. If the characteristics of distally and proximally sampled CSF are similar or correlate well, it may be possible to only sample CSF distally in the future, thereby avoiding the risks mentioned above.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with an EVD in place regardless of the underlying pathology.
Written informed consent to participate in the study must be obtained from the subject. If the subject is not capable of self-consent, all efforts will be made to locate a legally acceptable representative to act on behalf of the subject.
Disqualifiers
Patients in whom the removal of the drain is planned within 48 hours, before routine sampling, will be excluded.
Trial population
Patients with an external ventricular drain (EVD) presenting to the Neurosurgery ward.
Trial design
Other
Prospective
Treatments tested in this trial
Analyses of proximal and distal samples
Procedure/SurgeryEvaluate the difference between proximal and distal CSF samples
Treatment groups
Trial outcomes
Primary outcomes
Change of the CSF white cell count at day 1-4 and day 5-9 when comparing both sampling methods
The aim of the current study is to evaluate the difference between proximal and distal CSF sampling.
Secondary outcomes
White cell count correlation for all the available time points
Gram stain correlation for all the available time points
Culture correlation for all the available time points
Protein correlation for all the available time points
Sponsors and contacts
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