Edwards P, Farrell B, Lomas G, Mashru R, Ritchie N, Roberts I, Sandercock P, Wasserberg J, Yates D
CRASH Trial Coordinating Centre, London School of Hygiene and Tropical Medicine, London, UK.
Emerg Med J. 2002 Nov;19(6):510-4. doi: 10.1136/emj.19.6.510.
To test the design and feasibility of a large scale multicentre randomised controlled trial evaluating the efficacy and safety of a high dose corticosteroid infusion after head injury. To assess whether large numbers of patients could be enrolled and treated within eight hours from injury and then followed up at six months.
Randomised placebo controlled multicentre trial of a 48 hour corticosteroid infusion after significant head injury. All head injured adults who were observed while in hospital to have GCS of 14 or less (out of a maximum score of 15), and who were within eight hours of the injury, were eligible for trial entry. Analysis of baseline and outcome data (for both treatment groups combined) for 1000 patients enrolled in the pilot phase of the MRC CRASH Trial.
Fifty two hospitals in 14 countries participated in the pilot phase, recruiting an average of one patient per hospital per month. Of the 1000 randomised patients, 330 (33%) had mild head injury, 289 (29%) had moderate head injury, and 381 (38%) had severe head injury. Seven hundred and nine (71%) patients were randomised within three hours of injury. Outcome at two weeks from injury was known for 991 (99%) patients, of whom 170 (17%) patients died. At the time of writing, six month follow up for the first 500 patients was nearly complete. Vital status was known for 465 (93%) of the 500 patients, of whom 97 (21%) had died. Functional status based on the Glasgow Outcome Scale was known for 438 (88%) of the 500 patients: 21% were dead, 17% were severely disabled, 22% were moderately disabled, and 34% had made a good recovery.
The trial procedures proved practicable and a wide variety of patients were recruited in the emergency department within eight hours of injury. Using simple outcome measures, large numbers of patients can be successfully followed up.
检验一项大规模多中心随机对照试验的设计及可行性,该试验旨在评估头部受伤后大剂量皮质类固醇输注的疗效和安全性。评估是否能在受伤后八小时内招募并治疗大量患者,然后在六个月时进行随访。
对重度头部受伤后进行48小时皮质类固醇输注的随机安慰剂对照多中心试验。所有在医院观察到格拉斯哥昏迷量表(GCS)评分为14分或更低(满分15分)且受伤时间在八小时内的成年头部受伤患者均符合试验入组条件。对医学研究委员会颅脑损伤皮质类固醇随机化试验(MRC CRASH试验)试点阶段招募的1000名患者的基线和结局数据(两个治疗组合并)进行分析。
14个国家的52家医院参与了试点阶段,平均每家医院每月招募一名患者。在1000名随机分组的患者中,330名(33%)为轻度头部受伤,289名(29%)为中度头部受伤,381名(38%)为重度头部受伤。709名(71%)患者在受伤后三小时内被随机分组。991名(99%)患者在受伤两周时的结局已知,其中170名(17%)患者死亡。在撰写本文时,前500名患者的六个月随访已接近完成。500名患者中有465名(93%)的生命状态已知,其中97名(21%)死亡。基于格拉斯哥预后量表的功能状态在500名患者中有438名(88%)已知:21%死亡,17%严重残疾,22%中度残疾,34%恢复良好。
试验程序证明可行,且在受伤后八小时内在急诊科招募了各种各样的患者。使用简单的结局指标,可以成功随访大量患者。