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Hypothermia after cardiac arrest should be further evaluated: A systematic review of randomised trials with meta-analysis and trial sequential analysis
Högskolan i Borås, Institutionen för Vårdvetenskap.
Vise andre og tillknytning
2010 (engelsk)Inngår i: International Journal of Cardiology, ISSN 0167-5273, E-ISSN 1874-1754, Vol. 151, nr 3Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Background Guidelines recommend mild induced hypothermia (MIH) to reduce mortality and neurological impairment after out-of-hospital cardiac arrest. Our objective was to systematically evaluate the evidence for MIH taking into consideration the risks of systematic and random error and to GRADE the evidence. Methods Systematic review with meta-analysis and trial sequential analysis of randomised trials evaluating MIH after cardiac arrest in adults. We searched CENTRAL, MEDLINE, and EMBASE databases until May 2009. Retrieved trials were evaluated with Cochrane methodology. Meta-analytic estimates were calculated with random- and fixed-effects models and random errors were evaluated with trial sequential analysis (TSA). Results Five randomised trials (478 patients) were included. All trials had substantial risk of bias. The relative risk (RR) for death was 0.84 (95% confidence interval (CI) 0.70 to 1.01) and for poor neurological outcome 0.78 (95% CI 0.64 to 0.95). For the two trials with least risk of bias the RR for death was 0.92 (95% CI 0.56 to 1.51) and for poor neurological outcome 0.92 (95% confidence interval 0.56 to 1.50). TSA indicated lack of firm evidence for a beneficial effect. The substantial risk of bias and concerns with directness rated down the quality of the evidence to low. Conclusions Evidence regarding MIH after out-of-hospital cardiac arrest is still inconclusive and associated with non-negligible risks of systematic and random errors. Using GRADE-methodology, we conclude that the quality of evidence is low. Our findings demonstrate that clinical equipoise exists and that large well-designed randomised trials with low risk of bias are needed.

sted, utgiver, år, opplag, sider
Elsevier Ireland Ltd , 2010. Vol. 151, nr 3
HSV kategori
Identifikatorer
URN: urn:nbn:se:hb:diva-2994DOI: 10.1016/j.ijcard.2010.06.008Lokal ID: 2320/7394OAI: oai:DiVA.org:hb-2994DiVA, id: diva2:871089
Tilgjengelig fra: 2015-11-13 Laget: 2015-11-13 Sist oppdatert: 2017-12-06bibliografisk kontrollert

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