Systematic review of prediction of poor outcome in anoxic-ischaemic coma with biochemical markers of brain damage

Citation
Egj. Zandbergen et al., Systematic review of prediction of poor outcome in anoxic-ischaemic coma with biochemical markers of brain damage, INTEN CAR M, 27(10), 2001, pp. 1661-1667
Citations number
32
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
INTENSIVE CARE MEDICINE
ISSN journal
03424642 → ACNP
Volume
27
Issue
10
Year of publication
2001
Pages
1661 - 1667
Database
ISI
SICI code
0342-4642(200110)27:10<1661:SROPOP>2.0.ZU;2-R
Abstract
Objective: To investigate whether accurate prognostic rules can be derived from the combined results of studies concerning prediction of poor prognosi s in anoxic-ischaemic coma with biochemical markers of brain damage in cere brospinal fluid (CSF) or serum. Design: A meta-analysis of prognostic studies in anoxic-ischaemic coma, sel ected from Medline and EMBASE databases, according to predefined criteria. Subjects: Twenty-eight studies, with a total of 802 unselected, consecutive patients, in which tests, sampling time and outcome measures were describe d unequivocally and results were described using clear cut-off values or ra w data. Main outcome measures: Poor outcome, defined as death or vegetative state, versus good outcome, defined as any other outcome state. Analyses: The overall prognostic accuracy of these variables was expressed as the 95 % CIs of the pooled false-positive test rate and the pooled posit ive-likelihood ratios. Results: Only markers in CSF (creatine kinase isoenzyme (CKBB) > 204 U/l, n euron specific enolase (NSE) > 33 ng/ml, lactate dehydrogenase (LDH) > 82 U /l and glutamate oxaloacetate (GOT) > 62 U/l) reached a 0 % false-positive rate. However, due to small sample sizes, the confidence limits were wide. The accuracy of prediction of poor outcome seemed acceptably high for CSF-C KBB (pooled false-positive rate 0 % [95 % CI 0-2.3 % ]; pooled positive-lik elihood ratio 33.2 [95 % CI 4.8-230.2]), but this result was based on two r etrospective studies without blinding of the treating physicians for the te st result. Conclusions: Because of small numbers of patients studied and methodologica l limitations the combined results are not sufficiently accurate to provide a solid basis for nontreatment decisions.