Hypothermia in animal models of acute ischaemic stroke: a systematic review and meta-analysis

• Published in: Brain (London, England : 1878) England : 1878), 2007-12, Vol.130 (12), p.3063-3074
• Main Authors: van der Worp, H. Bart, Sena, Emily S., Donnan, Geoffrey A., Howells, David W., Macleod, Malcolm R.
• Format: Article
• Language: English
• Subjects: animal model; Animals; Biological and medical sciences; Biomedical Research - standards; Blood. Blood coagulation. Reticuloendothelial system; Brain Ischemia - therapy; Cerebral Infarction - pathology; Cerebral Infarction - prevention & control; Disease Models, Animal; hypothermia; Hypothermia, Induced - adverse effects; Hypothermia, Induced - methods; ischaemic stroke; Medical sciences; meta-analysis; Neurology; Pharmacology. Drug treatments; Stroke - therapy; Systematic review; Treatment Outcome; Vascular diseases and vascular malformations of the nervous system
• ISSN: 0006-8950; 1460-2156
• DOI: 10.1093/brain/awm083

Induced hypothermia is proposed as a treatment for acute ischaemic stroke, but there have been too few clinical trials involving too few patients to draw any conclusions about the therapeutic benefit of cooling. Animal studies of induced hypothermia in focal cerebral ischaemia have tested cooling throughout a wide range of target temperatures, durations and intervals between stroke onset and the initiation of hypothermia. These studies, therefore, provide an opportunity to evaluate the effectiveness of different treatment strategies in animal models to inform the design of future clinical trials. We performed a systematic review and meta-analysis of the evidence for efficacy of hypothermia in animal models of ischaemic stroke, and identified 101 publications reporting the effect of hypothermia on infarct size or functional outcome, including data from a total of 3353 animals. Overall, hypothermia reduced infarct size by 44% [95% confidence interval (CI), 40–47%]. Efficacy was highest with cooling to lower temperatures (≤31°C), where treatment was started before or at the onset of ischaemia and in temporary rather than permanent ischaemia models. However, a substantial reduction in infarct volume was also observed with cooling to 35°C (30%; 95% CI, 21–39%), with initiation of treatment between 90 and 180 min (37%; 95% CI, 28–46%) and in permanent ischaemia models (37%; 95% CI, 30–43%). The effects of hypothermia on functional outcome were broadly similar. We conclude that in animal models of focal cerebral ischaemia, hypothermia improves outcome by about one-third under conditions that may be achievable for large numbers of patients with ischaemic stroke. Large randomized clinical trials testing the effect of hypothermia in patients with acute ischaemic stroke are warranted.