To evaluate the incidence, causes and characteristics of meningitis and/or encephalitis in patients of all ages:1. To determine the causes of meningitis and/or encephalitis in children and adults2. To evaluate the clinical signs and symptoms and CSF…
ID
Source
Brief title
Condition
- Hepatobiliary neoplasms malignant and unspecified
- Central nervous system infections and inflammations
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
1. Detection of viruses and other micro-organisms in CSF, blood, nasopharyngeal
aspirates and feces
2. Clinical signs and symptoms as defined as: headache, fever, irritability,
altered consciousness, seizures, etc in relation to cause
3. Cell count, protein and glucose level of CSF and relation with causative
organism
4. Death or permanent sequellae due to meningitis/encephalitis
Secondary outcome
1. Costs, duration of hospitalization and antibiotic use due to
meningitis/encephalitis
Background summary
Meningitis (inflammation of the meninges) and encephalitis (inflammation of the
brain in association with clinical evidence of neurologic dysfunction) are
potential life-threatening conditions that can rapidly progress to permanent
brain damage, neurologic problems, and even death. Since vaccination against
the most common causative bacteria (H. influenza type b, S. pneumonia, N.
meningitidis serogroup C), the incidence of bacterial meningitis has dropped
significantly. Therefore, non-bacterial pathogens, such as viruses and
tick-born pathogens are increasingly recognized as important causes of central
nervous system (CNS) infections. In addition, immune-mediated processes (like
ADEM and antibody associated encephalitis) seem to play an important role. For
example, in a study in the UK, immune mediated processes were found in 20
percent of patients with encephalitis.
In contrast with bacterial meningitis, for which an extensive surveillance
system has been set up in many countries, viral or non-bacterial CNS infection
is not monitored systematically and proper incidence numbers of the different
causative agents and mortality and morbidity rates are missing. Recently it has
been propagated that it is important to optimize the surveillance for viral
encephalitis/meningitis in Europe to gain more insight in the aetiological
pattern as well as to optimize therapy to improve survival and reduce brain
injury.
The aim of this project is to set up a regional pilot survey study that will
systematically register both clinical and laboratory findings of adults and
children with meningitis and/or encephalitis in the Netherlands to gain more
insight in the causes and pathogenesis of these diseases. After one year, the
results of the pilot survey will be evaluated to assess if the study will be
set up nationwide (in the Netherlands).
Study objective
To evaluate the incidence, causes and characteristics of meningitis and/or
encephalitis in patients of all ages:
1. To determine the causes of meningitis and/or encephalitis in children and
adults
2. To evaluate the clinical signs and symptoms and CSF (and other material)
laboratory characteristics of children and adults with a diagnosis of
meningitis and/or encephalitis
3. To determine what materials (CSF, blood, faeces/rectal swab, nasopharyngeal
aspirate/swab or throat swab) are most suitable for the detection of
meningitis/encephalitis in children and adults.
4. To determine the impact of meningitis and/or encephalitis on the health care
systems in terms of costs, antibiotic use, morbidity and mortality.
Study design
This is a prospective observational study. A pilot (duration 1 year) will be
initiated in 3 regional hospitals in Amsterdam and Almere, the Netherlands. If
this pilot is successfull, the study will be extended to the whole country.
Study burden and risks
The burden consists of the collection of one bloodsample, one throatswab or
nasopharyngeal aspirate and one faecessample or rectal swab.
The extent of this burden is estimated as low. As far as we know, there are no
risks of the above mentioned collection of materials.
Meibergdreef 9
1100 DD Amsterdam
NL
Meibergdreef 9
1100 DD Amsterdam
NL
Listed location countries
Age
Inclusion criteria
Patients of all ages (including premature born infants) with a clinical suspicion of meningitis or encephalitis of whom central spine fluid is obtained, are eligible for inclusion in this study.
Exclusion criteria
- neurosurgical operation in recent past (last 3 months)
- drain with connection to cerebrospinal fluid
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL36747.018.11 |