Pucci E, Branãs P, D'Amico R, Giuliani G, Solari A, Taus C
ASUR Marche - Zona Territoriale 9, U.O. Neurologia - Ospedale di Macerata, Via Santa Lucia, 3, Macerata, Italy, 62100.
Cochrane Database Syst Rev. 2007 Jan 24;2007(1):CD002818. doi: 10.1002/14651858.CD002818.pub2.
Fatigue is one of the most common and disabling symptoms of people with Multiple Sclerosis (MS). The effective management of fatigue has an important impact on the patient's functioning, abilities, and quality of life. Although a number of strategies have been devised for reducing fatigue, treatment recommendations are based on a limited amount of scientific evidence. Many textbooks report amantadine as a first-choice drug for MS-related fatigue because of published randomised controlled trials (RCTs) showing some benefit.
To determine the effectiveness and safety of amantadine in treating fatigue in people with MS.
We searched The Cochrane MS Group Trials Register (July 2006), The Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library, Issue 1, 2006), MEDLINE (January 1966 to July 2006), EMBASE (January 1974 to July 2006), bibliographies of relevant articles and handsearched relevant journals. We also contacted drug companies and researchers in the field.
Randomised, placebo or other drugs-controlled, double-blind trials of amantadine in MS people with fatigue.
Three reviewers selected studies for inclusion in the review and they extracted the data reported in the original articles. We requested missing and unclear data by correspondence with the trial's principal investigator. A meta-analysis was not performed due to the inadequacy of available data and heterogeneity of outcome measures.
Out of 13 pertinent publications, 5 trials met the criteria for inclusion in this review: one study was a parallel arms study, and 4 were crossover trials. The number of randomised participants ranged between 10 and 115, and a total of 272 MS patients were studied. Overall the quality of the studies considered was poor and all trials were open to bias. All studies reported small and inconsistent improvements in fatigue, whereas the clinical relevance of these findings and the impact on patient's functioning and health related quality of life remained undetermined. The number of participants reporting side effects during amantadine therapy ranged from 10% to 57%.
AUTHORS' CONCLUSIONS: The efficacy of amantadine in reducing fatigue in people with MS is poorly documented, as well as its tolerability. It is advisable to: (1) improve knowledge on the underlying mechanisms of MS-related fatigue; (2) achieve anagreement on accurate, reliable and responsive outcome measures of fatigue; (3) perform good quality RCTs.
疲劳是多发性硬化症(MS)患者最常见且使人衰弱的症状之一。有效管理疲劳对患者的功能、能力及生活质量有重要影响。尽管已制定了多种减轻疲劳的策略,但治疗建议所依据的科学证据有限。许多教科书将金刚烷胺列为治疗MS相关疲劳的首选药物,因为已发表的随机对照试验(RCT)显示其有一定益处。
确定金刚烷胺治疗MS患者疲劳的有效性和安全性。
我们检索了Cochrane MS小组试验注册库(2006年7月)、Cochrane对照试验中央注册库(CENTRAL)(Cochrane图书馆,2006年第1期)、MEDLINE(1966年1月至2006年7月)、EMBASE(1974年1月至2006年7月)、相关文章的参考文献,并手工检索了相关期刊。我们还联系了该领域的制药公司和研究人员。
金刚烷胺治疗MS疲劳患者的随机、安慰剂或其他药物对照、双盲试验。
三位综述作者选择纳入综述的研究,并提取原始文章中报告的数据。我们通过与试验主要研究者通信索取缺失和不清楚的数据。由于现有数据不足和结局指标的异质性,未进行荟萃分析。
在13篇相关出版物中,5项试验符合纳入本综述的标准:1项研究为平行组研究,4项为交叉试验。随机参与者人数在10至115之间,共研究了272例MS患者。总体而言,所纳入研究的质量较差,所有试验都存在偏倚风险。所有研究均报告疲劳有小幅度且不一致的改善,而这些结果的临床相关性以及对患者功能和健康相关生活质量的影响仍未确定。在金刚烷胺治疗期间报告有副作用的参与者人数在10%至57%之间。
金刚烷胺减轻MS患者疲劳的疗效以及耐受性的文献记载不足。建议:(1)增进对MS相关疲劳潜在机制的了解;(2)就准确、可靠且灵敏的疲劳结局指标达成共识;(3)开展高质量的随机对照试验。