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儿童严重创伤性脑损伤后低温与常温治疗的比较(Cool Kids):一项 3 期随机对照试验。

Comparison of hypothermia and normothermia after severe traumatic brain injury in children (Cool Kids): a phase 3, randomised controlled trial.

机构信息

Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ 85016, USA.

出版信息

Lancet Neurol. 2013 Jun;12(6):546-53. doi: 10.1016/S1474-4422(13)70077-2. Epub 2013 May 8.

Abstract

BACKGROUND

On the basis of mixed results from previous trials, we assessed whether therapeutic hypothermia for 48-72 h with slow rewarming improved mortality in children after brain injury.

METHODS

In this phase 3, multicenter, multinational, randomised controlled trial, we included patients with severe traumatic brain injury who were younger than 18 years and could be enrolled within 6 h of injury. We used a computer-generated randomisation sequence to randomly allocate patients (1:1; stratified by site and age [<6 years, 6-15 years, 16-17 years]) to either hypothermia (rapidly cooled to 32-33°C for 48-72 h, then rewarmed by 0·5-1·0°C every 12-24 h) or normothermia (maintained at 36·5-37·5°C). The primary outcome was mortality at 3 months, assessed by intention-to-treat analysis; secondary outcomes were global function at 3 months after injury using the Glasgow outcome scale (GOS) and the GOS-extended pediatrics, and the occurrence of serious adverse events. Investigators assessing outcomes were masked to treatment. This trial is registered with ClinicalTrials.gov, number NCT00222742.

FINDINGS

The study was terminated early for futility after an interim data analysis on data for 77 patients (enrolled between Nov 1, 2007, and Feb 28, 2011): 39 in the hypothermia group and 38 in the normothermia group. We detected no between-group difference in mortality 3 months after injury (6 [15%] of 39 patients in the hypothermia group vs two [5%] of 38 patients in the normothermia group; p=0·15). Poor outcomes did not differ between groups (in the hypothermia group, 16 [42%] patients had a poor outcome by GOS and 18 [47%] had a poor outcome by GOS-extended paediatrics; in the normothermia group, 16 [42%] patients had a poor outcome by GOS and 19 [51%] of 37 patients had a poor outcome by GOS-extended paediatrics). We recorded no between-group differences in the occurrence of adverse events or serious adverse events.

INTERPRETATION

Hypothermia for 48 h with slow rewarming does not reduce mortality of improve global functional outcome after paediatric severe traumatic brain injury.

FUNDING

National Institute of Neurological Disorders and Stroke and National Institutes of Health.

摘要

背景

基于以往试验的混合结果,我们评估了 48-72 小时的治疗性低温伴缓慢复温是否能改善颅脑损伤后儿童的死亡率。

方法

在这项 3 期、多中心、多国、随机对照试验中,我们纳入了年龄小于 18 岁且可在损伤后 6 小时内入组的严重创伤性颅脑损伤患者。我们使用计算机生成的随机序列将患者(1:1;按部位和年龄分层 [<6 岁、6-15 岁、16-17 岁])随机分配至低温组(快速降至 32-33°C 持续 48-72 小时,然后以 0.5-1.0°C/每 12-24 小时的速度缓慢复温)或常温组(维持在 36.5-37.5°C)。主要结局为 3 个月时的死亡率,采用意向治疗分析进行评估;次要结局为损伤后 3 个月时使用格拉斯哥结局量表(GOS)和扩展儿科 GOS 的总体功能,以及严重不良事件的发生情况。评估结局的研究者对治疗情况设盲。本试验在 ClinicalTrials.gov 注册,编号为 NCT00222742。

结果

在对 77 例患者(于 2007 年 11 月 1 日至 2011 年 2 月 28 日期间入组)的数据进行中期分析后,该研究因无效而提前终止:低温组 39 例,常温组 38 例。我们未发现两组在损伤后 3 个月时死亡率存在差异(低温组 6 [15%]例患者死亡,常温组 2 [5%]例患者死亡;p=0.15)。两组间不良结局无差异(低温组中,16 [42%]例患者 GOS 评分不良,18 [47%]例患者 GOS 扩展儿科评分不良;常温组中,16 [42%]例患者 GOS 评分不良,19 [51%]例患者 GOS 扩展儿科评分不良)。我们未发现两组间不良事件或严重不良事件的发生存在差异。

解释

48 小时的低温伴缓慢复温并不能降低儿科严重创伤性颅脑损伤患者的死亡率或改善总体功能结局。

资金来源

美国国立神经病学与卒中研究所和美国国立卫生研究院。

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