JFK Johnson Rehabilitation Institute, Edison, NJ, USA.
N Engl J Med. 2012 Mar 1;366(9):819-26. doi: 10.1056/NEJMoa1102609.
Amantadine hydrochloride is one of the most commonly prescribed medications for patients with prolonged disorders of consciousness after traumatic brain injury. Preliminary studies have suggested that amantadine may promote functional recovery.
We enrolled 184 patients who were in a vegetative or minimally conscious state 4 to 16 weeks after traumatic brain injury and who were receiving inpatient rehabilitation. Patients were randomly assigned to receive amantadine or placebo for 4 weeks and were followed for 2 weeks after the treatment was discontinued. The rate of functional recovery on the Disability Rating Scale (DRS; range, 0 to 29, with higher scores indicating greater disability) was compared over the 4 weeks of treatment (primary outcome) and during the 2-week washout period with the use of mixed-effects regression models.
During the 4-week treatment period, recovery was significantly faster in the amantadine group than in the placebo group, as measured by the DRS score (difference in slope, 0.24 points per week; P=0.007), indicating a benefit with respect to the primary outcome measure. In a prespecified subgroup analysis, the treatment effect was similar for patients in a vegetative state and those in a minimally conscious state. The rate of improvement in the amantadine group slowed during the 2 weeks after treatment (weeks 5 and 6) and was significantly slower than the rate in the placebo group (difference in slope, 0.30 points per week; P=0.02). The overall improvement in DRS scores between baseline and week 6 (2 weeks after treatment was discontinued) was similar in the two groups. There were no significant differences in the incidence of serious adverse events.
Amantadine accelerated the pace of functional recovery during active treatment in patients with post-traumatic disorders of consciousness. (Funded by the National Institute on Disability and Rehabilitation Research; ClinicalTrials.gov number, NCT00970944.).
盐酸金刚烷胺是颅脑损伤后长时间意识障碍患者最常开的处方之一。初步研究表明,金刚烷胺可能促进功能恢复。
我们纳入了 184 名颅脑损伤后 4 至 16 周处于植物状态或最小意识状态的患者,并对其进行住院康复治疗。患者被随机分配接受金刚烷胺或安慰剂治疗 4 周,并在停药后 2 周进行随访。使用混合效应回归模型比较治疗 4 周(主要结局)和停药 2 周期间残疾评定量表(DRS;范围 0 至 29,分数越高表示残疾越严重)的功能恢复率。
在治疗 4 周期间,与安慰剂组相比,金刚烷胺组的 DRS 评分恢复更快(斜率差异,每周 0.24 分;P=0.007),这表明在主要结局测量上有获益。在预先指定的亚组分析中,金刚烷胺对植物状态和最小意识状态患者的治疗效果相似。治疗组在治疗结束后 2 周(第 5 和第 6 周)的改善速度减慢,且明显慢于安慰剂组(斜率差异,每周 0.30 分;P=0.02)。两组患者从基线到第 6 周(治疗结束后 2 周)的 DRS 评分总体改善相似。严重不良事件的发生率无显著差异。
金刚烷胺在创伤后意识障碍患者的积极治疗中加速了功能恢复的速度。(由国立残疾和康复研究所资助;临床试验.gov 编号:NCT00970944。)