Taricco M, Pagliacci M C, Telaro E, Adone R
Functional Recovery and Rehabilitation Unit, G. Salvini Hospital, Passirana di Rho, Milan, Italy.
Eura Medicophys. 2006 Mar;42(1):5-15.
The aim of this paper was to assess the effectiveness and safety of baclofen, dantrolene, tizanidine and any other drugs for the treatment of long-term spasticity in spinal cord injury (SCI) patients, as well as the effectiveness and safety of different routes of administration of baclofen. A systematic review of randomised controlled trials (RCTs), within the Cochrane Collaboration Injuries Group, was carried out. The Cochrane Injuries Group Specialised Register, the Cochrane Controlled Trials Register, MEDLINE, EMBASE and CINAHL were searched up to July 2006 without language restriction. Drug companies and experts active in the area were also contacted to find other relevant studies. Two investigators independently identified relevant studies, extracted data and assessed methodological quality of studies resolving disagreement by consensus. Nine out of 55 studies met the inclusion criteria. The heterogeneity among studies did not allow quantitative combination of
Study designs were: 8 crossover, 1 parallel-group trial. Two studies (14 SCI patients) showed a significant effect of intrathecal baclofen in reducing spasticity (Ashworth score and activities of daily living [ADL] performances), compared to placebo, without any adverse effect. The study comparing tizanidine to placebo (118 SCI patients) showed a significant effect of tizanidine in improving Ashworth score but not in ADL performances. The tizanidine group reported significant rates of adverse effects (drowsiness, xerostomia). For the other drugs (gabapentine, clonidine, diazepam, amytal and oral baclofen) the results do not provide evidence for a clinical significant effectiveness. This systematic review indicates that there is insufficient evidence to assist clinicians in a rational approach to antispastic treatment for SCI. Further research is urgently needed to improve the scientific basis of patient care.
本文旨在评估巴氯芬、丹曲林、替扎尼定及其他任何药物治疗脊髓损伤(SCI)患者长期痉挛的有效性和安全性,以及巴氯芬不同给药途径的有效性和安全性。在Cochrane协作损伤组内进行了随机对照试验(RCT)的系统评价。检索了Cochrane损伤组专业注册库、Cochrane对照试验注册库、MEDLINE、EMBASE和CINAHL直至2006年7月,无语言限制。还联系了该领域的制药公司和专家以查找其他相关研究。两名研究者独立识别相关研究、提取数据并评估研究的方法学质量,通过共识解决分歧。55项研究中有9项符合纳入标准。研究间的异质性不允许进行定量合并。
研究设计为:8项交叉试验,1项平行组试验。两项研究(14例SCI患者)显示,与安慰剂相比,鞘内注射巴氯芬在降低痉挛(Ashworth评分和日常生活活动[ADL]表现)方面有显著效果,且无任何不良反应。比较替扎尼定与安慰剂的研究(118例SCI患者)显示,替扎尼定在改善Ashworth评分方面有显著效果,但在ADL表现方面无显著效果。替扎尼定组报告的不良反应发生率较高(嗜睡、口干)。对于其他药物(加巴喷丁、可乐定、地西泮、异戊巴比妥和口服巴氯芬),结果未提供临床显著有效性的证据。该系统评价表明,没有足够的证据帮助临床医生以合理的方法进行SCI抗痉挛治疗。迫切需要进一步研究以改善患者护理的科学依据。