Willis C, Lybrand S, Bellamy N
Centre Of National Research On Disability and Rehabilitation Medicine, University of Queensland, Level 3, Mayne Medical School, Herston Road, Brisbane, Queensland, Australia.
Cochrane Database Syst Rev. 2004;2003(1):CD003986. doi: 10.1002/14651858.CD003986.pub2.
Glutamate is the principal excitatory neurotransmitter in the brain. Injury to the brain can cause an ionic imbalance in cerebral tissue, creating an excitotoxic cascade involving glutamate and other excitatory amino acids, that leads to neuronal death in the tissue surrounding the original injury site. Research has centred around inhibiting this increase in excitatory amino acid during injury either pre- or post-synaptically. Animal studies appeared promising, but as yet, those results have not been repeated in human clinical trials.
To assess systematically the efficacy of excitatory amino acid inhibitors on improving patient outcome following traumatic brain injury.
Online searches of the databases; CENTRAL, MEDLINE, EMBASE, IDdb3, and Science Citation Index. Online searches of clinical trial registers. General online searches of the Internet. Authors of published works and associated pharmaceutical companies were contacted.
Trials were included if they were randomised, double-blind, controlled trials where excitatory amino acid inhibitors were administered to patients with traumatic brain injury, within 24 hours of sustaining that injury, and compared to a control group.
Twelve trials, involving eight compounds, were identified that appeared to fit the inclusion criteria. Further investigation excluded three of these trials. Two of the remaining trials are ongoing. Of the seven included studies, one trial did not report GOS data and we were unable to acquire them. Three trials have not been published and the data were not made available to us. One trial is currently being prepared for publication, leaving two trials where data were available. Data were extracted by two independent reviewers.
Data were available for two of the seven relevant trials identified, with 760 recruited participants. Mortality is similar between patients who receive excitatory amino acid inhibitors and those that receive placebo: odds ratio (OR) 1.11; 95% confidence interval (CI) 0.78, 1.60. Patients who have a favourable outcome six months after injury are also similar between treatment and placebo groups: OR 0.86; 95% CI 0.64, 1.16.
REVIEWER'S CONCLUSIONS: The case for efficacy of excitatory amino acid inhibitor therapy remains unproven. To date, no product has proven to be efficacious (as determined by the criteria applied) for improving the outcomes of brain-injured patients. Early termination, unpublished, and underpowered studies limit a clear appreciation of the merits of this form of intervention. Additional studies, some of which remain in progress, may more clearly define the efficacy and effectiveness issues.
谷氨酸是大脑中主要的兴奋性神经递质。脑损伤可导致脑组织中的离子失衡,引发涉及谷氨酸和其他兴奋性氨基酸的兴奋毒性级联反应,进而导致原损伤部位周围组织中的神经元死亡。研究主要围绕在损伤发生前或后突触处抑制兴奋性氨基酸的这种增加。动物研究看起来很有前景,但截至目前,这些结果尚未在人类临床试验中得到重复验证。
系统评估兴奋性氨基酸抑制剂对改善创伤性脑损伤患者预后的疗效。
对CENTRAL、MEDLINE、EMBASE、IDdb3和科学引文索引等数据库进行在线检索。对临床试验注册库进行在线检索。在互联网上进行一般性在线检索。联系已发表作品的作者及相关制药公司。
纳入的试验需为随机、双盲、对照试验,其中在创伤性脑损伤患者受伤后24小时内给予兴奋性氨基酸抑制剂,并与对照组进行比较。
共识别出12项涉及8种化合物的试验,这些试验似乎符合纳入标准。进一步调查排除了其中3项试验。其余2项试验正在进行中。在纳入的7项研究中,有1项试验未报告格拉斯哥预后评分(GOS)数据,且我们无法获取这些数据。3项试验未发表,其数据未提供给我们。1项试验目前正在准备发表,因此仅有2项试验有可用数据。数据由两名独立的评审员提取。
在识别出的7项相关试验中,有2项试验有可用数据,共招募了760名参与者。接受兴奋性氨基酸抑制剂治疗的患者与接受安慰剂治疗的患者死亡率相似:比值比(OR)为1.11;95%置信区间(CI)为0.78至1.60。治疗组和安慰剂组中伤后6个月预后良好的患者比例也相似:OR为0.86;95%CI为0.64至1.16。
兴奋性氨基酸抑制剂治疗的疗效尚无定论。迄今为止,尚无产品被证明(根据所应用的标准判断)对改善脑损伤患者的预后有效。早期终止试验、未发表的试验以及样本量不足的研究限制了对这种干预形式优点的清晰认识。一些仍在进行中的其他研究可能会更明确地界定疗效和有效性问题。