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首页> 外文期刊>The American heart journal >Target temperature management after out-of-hospital cardiac arrest - A randomized, parallel-group, assessor-blinded clinical trial - Rationale and design
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Target temperature management after out-of-hospital cardiac arrest - A randomized, parallel-group, assessor-blinded clinical trial - Rationale and design

机译:院外心脏骤停后的目标温度管理-随机,平行组,评估者盲的临床试验-原理和设计

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摘要

Background: Experimental animal studies and previous randomized trials suggest an improvement in mortality and neurologic function with induced hypothermia after cardiac arrest. International guidelines advocate the use of a target temperature management of 32°C to 34°C for 12 to 24 hours after resuscitation from out-of-hospital cardiac arrest. A systematic review indicates that the evidence for recommending this intervention is inconclusive, and the GRADE level of evidence is low. Previous trials were small, with high risk of bias, evaluated select populations, and did not treat hyperthermia in the control groups. The optimal target temperature management strategy is not known. Methods: The TTM trial is an investigator-initiated, international, randomized, parallel-group, and assessor-blinded clinical trial designed to enroll at least 850 adult, unconscious patients resuscitated after out-of-hospital cardiac arrest of a presumed cardiac cause. The patients will be randomized to a target temperature management of either 33°C or 36°C after return of spontaneous circulation. In both groups, the intervention will last 36 hours. The primary outcome is all-cause mortality at maximal follow-up. The main secondary outcomes are the composite outcome of all-cause mortality and poor neurologic function (cerebral performance categories 3 and 4) at hospital discharge and at 180 days, cognitive status and quality of life at 180 days, assessment of safety and harm. Discussion: The TTM trial will investigate potential benefit and harm of 2 target temperature strategies, both avoiding hyperthermia in a large proportion of the out-of-hospital cardiac arrest population.
机译:背景:实验动物研究和先前的随机试验表明,心脏骤停后诱发体温过低会降低死亡率和神经系统功能。国际准则主张从院外心脏骤停复苏后的12至24小时内,将目标温度控制在32°C至34°C之间。系统的审查表明,推荐这种干预措施的证据尚无定论,GRADE的证据水平很低。以前的试验很小,有偏见的风险很高,评估了部分人群,并且未在对照组中治疗体温过高。最佳目标温度管理策略未知。方法:TTM试验是一项由研究人员发起的国际随机,平行分组,评估者盲目的临床试验,旨在招募至少850名因院外心脏骤停而因推测的心脏原因而复苏的成人无意识患者。自发性循环后,患者将被随机分配至目标温度控制为33°C或36°C。在这两组中,干预将持续36个小时。主要结果是最大随访时的全因死亡率。主要的次要结局是出院时和180天时全因死亡率和神经系统功能不佳(脑功能类别3和4)的综合结果,在180天时的认知状态和生活质量,评估安全性和伤害。讨论:TTM试验将研究两种目标温度策略的潜在利弊,这两种方法都可以在医院外心脏骤停人群中避免大部分的体温过高。

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