ABSTRACT
On a theoretical background, hypothermia surmounts pharmacological neuroprotection by providing simultaneous effects on several mechanisms potentially relevant in the postischemic maturation of the damage. Measurements of the infarct size in animal models reveal that mild hypothermia is probably one of the most effective and documented neuroprotective intervention, both in focal and global ischemia models. As expected, hypothermia is more effective, and the results more consistent, when the time window for initiation of treatment is shorter than 6 h, with an apparent correlation between effect size and time window in the range of 0-6 h. There seems to be also an inverse relationship between temperature depth and reduction in infarct size. Mild hypothermia, such as cooling by 1°C or 2°C, is still associated with a noteworthy 20%–30% infarct size reduction.
