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首页> 外文期刊>Trials >European society of intensive care medicine study of therapeutic hypothermia (32-35°C) for intracranial pressure reduction after traumatic brain injury (the Eurotherm3235Trial)
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European society of intensive care medicine study of therapeutic hypothermia (32-35°C) for intracranial pressure reduction after traumatic brain injury (the Eurotherm3235Trial)

机译:欧洲重症医学会研究低温治疗(32-35°C),以减轻颅脑外伤后的颅内压(Eurotherm3235Trial)

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Background Traumatic brain injury is a major cause of death and severe disability worldwide with 1,000,000 hospital admissions per annum throughout the European Union. Therapeutic hypothermia to reduce intracranial hypertension may improve patient outcome but key issues are length of hypothermia treatment and speed of re-warming. A recent meta-analysis showed improved outcome when hypothermia was continued for between 48 hours and 5 days and patients were re-warmed slowly (1°C/4 hours). Previous experience with cooling also appears to be important if complications, which may outweigh the benefits of hypothermia, are to be avoided. Methods/design This is a pragmatic, multi-centre randomised controlled trial examining the effects of hypothermia 32-35°C, titrated to reduce intracranial pressure Participants are randomised to either standard care or standard care with titrated therapeutic hypothermia. Hypothermia is initiated with 20-30 ml/kg of intravenous, refrigerated 0.9% saline and maintained using each centre's usual cooling technique. There is a guideline for detection and treatment of shivering in the intervention group. Hypothermia is maintained for at least 48 hours in the treatment group and continued for as long as is necessary to maintain intracranial pressure 20 mmHg in accordance with the Brain Trauma Foundation Guidelines, 2007. Discussion The Eurotherm3235Trial is the most important clinical trial in critical care ever conceived by European intensive care medicine, because it was launched and funded by the European Society of Intensive Care Medicine and will be the largest non-commercial randomised controlled trial due to the substantial number of centres required to deliver the target number of patients. It represents a new and fundamental step for intensive care medicine in Europe. Recruitment will continue until January 2013 and interested clinicians from intensive care units worldwide can still join this important collaboration by contacting the Trial Coordinating Team via the trial website http://www.eurotherm3235trial.eu webcite . Trial registration Current Controlled Trials ISRCTN34555414
机译:背景技术外伤性脑损伤是全球范围内死亡和严重残疾的主要原因,在整个欧盟,每年有1,000,000例住院病人。降低颅内高压的治疗性体温过低可能会改善患者的预后,但关键问题是体温过低的治疗时间和复温的速度。最近的一项荟萃​​分析显示,持续低温治疗48小时至5天且患者重新缓慢升温(1°C / 4小时)时,预后得到改善。如果要避免可能超过体温过高的并发症,那么以前的冷却经验也很重要。方法/设计这是一个实用的,多中心的随机对照试验,研究了在32-35°C下进行低温治疗的效果,并进行了滴定以降低颅内压。参与者被随机分配到标准治疗或采用滴定性治疗性低温治疗的标准治疗。用20-30 ml / kg的0.9%冷藏生理盐水静脉注射开始低温治疗,并使用每个中心的常规冷却技术进行维持。在干预组中有用于检测和治疗发抖的指南。根据2007年《脑部创伤基金会指南》的规定,治疗组的体温过低症至少维持48小时,并持续必要的时间以保持颅内压20 mmHg。由欧洲重症监护医学构想,因为它是由欧洲重症监护医学会发起并资助的,由于要达到目标患者数量需要大量中心,因此它将是最大的非商业性随机对照试验。它代表了欧洲重症监护医学的新的基础性步骤。招聘将一直持续到2013年1月,来自全球重症监护室的有兴趣的临床医生仍可以通过试验网站http://www.eurotherm3235trial.eu webcite与试验协调小组联系,以加入这一重要合作。试用注册电流对照试验ISRCTN34555414

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