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Hypothermia therapy after traumatic brain injury in children
James S Hutchison1, Roxanne E Ward, Jacques Lacroix
1Department of Critical Care Medicine, Hospital for Sick Children, 555 University Ave., Toronto, ON M5G 1X8, Canada. jamie.hutchison@sickkids.ca
Insights
Hypothermia therapy for severe traumatic brain injury in children did not improve neurologic outcomes and may increase mortality. This study found a higher rate of unfavorable outcomes and deaths in the hypothermia group compared to normothermia.
Area of Science:
- Pediatric critical care medicine
- Neurotrauma research
- Therapeutic hypothermia
Background:
- Hypothermia therapy shows promise in animal models for traumatic brain injury (TBI).
- The efficacy of hypothermia in improving neurologic outcomes and survival in children with severe TBI remains unestablished.
Purpose of the Study:
- To investigate the effect of hypothermia therapy on neurologic outcomes and mortality in children with severe traumatic brain injury.
- To compare outcomes between children treated with hypothermia and those receiving normothermia.
Main Methods:
- A multicenter, international randomized trial involving children with severe TBI.
- Children were assigned to either hypothermia therapy (32.5°C for 24 hours) or normothermia (37.0°C), initiated within 8 hours post-injury.
- The primary outcome was an unfavorable neurologic outcome (severe disability, vegetative state, or death) at 6 months, assessed by the Pediatric Cerebral Performance Category score.
Main Results:
- 31% of patients in the hypothermia group experienced an unfavorable outcome versus 22% in the normothermia group (P=0.14).
- Mortality was higher in the hypothermia group (21%) compared to the normothermia group (12%) (P=0.06).
- Increased instances of hypotension and need for vasoactive agents were observed during rewarming in the hypothermia group.
Conclusions:
- Hypothermia therapy initiated within 8 hours and continued for 24 hours does not improve neurologic outcomes in children with severe TBI.
- Hypothermia therapy may potentially increase mortality rates in this pediatric population.
- Further research is needed to clarify the role and safety of hypothermia in pediatric TBI management.
Background:
Hypothermia therapy improves survival and the neurologic outcome in animal models of traumatic brain injury. However, the effect of hypothermia therapy on the neurologic outcome and mortality among children who have severe traumatic brain injury is unknown.
Methods:
In a multicenter, international trial, we randomly assigned children with severe traumatic brain injury to either hypothermia therapy (32.5 degrees C for 24 hours) initiated within 8 hours after injury or to normothermia (37.0 degrees C). The primary outcome was the proportion of children who had an unfavorable outcome (i.e., severe disability, persistent vegetative state, or death), as assessed on the basis of the Pediatric Cerebral Performance Category score at 6 months.
Results:
A total of 225 children were randomly assigned to the hypothermia group or the normothermia group; the mean temperatures achieved in the two groups were 33.1+/-1.2 degrees C and 36.9+/-0.5 degrees C, respectively. At 6 months, 31% of the patients in the hypothermia group, as compared with 22% of the patients in the normothermia group, had an unfavorable outcome (relative risk, 1.41; 95% confidence interval [CI], 0.89 to 2.22; P=0.14). There were 23 deaths (21%) in the hypothermia group and 14 deaths (12%) in the normothermia group (relative risk, 1.40; 95% CI, 0.90 to 2.27; P=0.06). There was more hypotension (P=0.047) and more vasoactive agents were administered (P<0.001) in the hypothermia group during the rewarming period than in the normothermia group. Lengths of stay in the intensive care unit and in the hospital and other adverse events were similar in the two groups.
Conclusions:
In children with severe traumatic brain injury, hypothermia therapy that is initiated within 8 hours after injury and continued for 24 hours does not improve the neurologic outcome and may increase mortality. (Current Controlled Trials number, ISRCTN77393684 [controlled-trials.com].).
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