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阿米替林用于治疗成人神经性疼痛。

Amitriptyline for neuropathic pain in adults.

作者信息

Moore R Andrew, Derry Sheena, Aldington Dominic, Cole Peter, Wiffen Philip J

机构信息

Pain Research and Nuffield Department of Clinical Neurosciences (Nuffield Division of Anaesthetics), University of Oxford, Pain Research Unit, Churchill Hospital, Oxford, Oxfordshire, UK, OX3 7LE.

出版信息

Cochrane Database Syst Rev. 2015 Jul 6;2015(7):CD008242. doi: 10.1002/14651858.CD008242.pub3.

Abstract

BACKGROUND

This is an updated version of the original Cochrane review published in Issue 12, 2012. That review considered both fibromyalgia and neuropathic pain, but the effects of amitriptyline for fibromyalgia are now dealt with in a separate review.Amitriptyline is a tricyclic antidepressant that is widely used to treat chronic neuropathic pain (pain due to nerve damage). It is recommended as a first line treatment in many guidelines. Neuropathic pain can be treated with antidepressant drugs in doses below those at which the drugs act as antidepressants.

OBJECTIVES

To assess the analgesic efficacy of amitriptyline for relief of chronic neuropathic pain, and the adverse events associated with its use in clinical trials.

SEARCH METHODS

We searched CENTRAL, MEDLINE, and EMBASE to March 2015, together with two clinical trial registries, and the reference lists of retrieved papers, previous systematic reviews, and other reviews; we also used our own hand searched database for older studies.

SELECTION CRITERIA

We included randomised, double-blind studies of at least four weeks' duration comparing amitriptyline with placebo or another active treatment in chronic neuropathic pain conditions.

DATA COLLECTION AND ANALYSIS

We performed analysis using three tiers of evidence. First tier evidence derived from data meeting current best standards and subject to minimal risk of bias (outcome equivalent to substantial pain intensity reduction, intention-to-treat analysis without imputation for dropouts; at least 200 participants in the comparison, 8 to 12 weeks' duration, parallel design), second tier from data that failed to meet one or more of these criteria and were considered at some risk of bias but with adequate numbers in the comparison, and third tier from data involving small numbers of participants that were considered very likely to be biased or used outcomes of limited clinical utility, or both.

MAIN RESULTS

We included 15 studies from the earlier review and two new studies (17 studies, 1342 participants) in seven neuropathic pain conditions. Eight cross-over studies with 302 participants had a median of 36 participants, and nine parallel group studies with 1040 participants had a median of 84 participants. Study quality was modest, though most studies were at high risk of bias due to small size.There was no first-tier or second-tier evidence for amitriptyline in treating any neuropathic pain condition. Only third-tier evidence was available. For only two of seven studies reporting useful efficacy data was amitriptyline significantly better than placebo (very low quality evidence).More participants experienced at least one adverse event; 55% of participants taking amitriptyline and 36% taking placebo. The risk ratio (RR) was 1.5 (95% confidence interval (CI) 1.3 to 1.8) and the number needed to treat for an additional harmful outcome was 5.2 (3.6 to 9.1) (low quality evidence). Serious adverse events were rare. Adverse event and all-cause withdrawals were not different, but were rarely reported (very low quality evidence).

AUTHORS' CONCLUSIONS: Amitriptyline has been a first-line treatment for neuropathic pain for many years. The fact that there is no supportive unbiased evidence for a beneficial effect is disappointing, but has to be balanced against decades of successful treatment in many people with neuropathic pain. There is no good evidence of a lack of effect; rather our concern should be of overestimation of treatment effect. Amitriptyline should continue to be used as part of the treatment of neuropathic pain, but only a minority of people will achieve satisfactory pain relief. Limited information suggests that failure with one antidepressant does not mean failure with all.

摘要

背景

这是2012年第12期发表的原始Cochrane系统评价的更新版本。该评价同时考虑了纤维肌痛和神经性疼痛,但阿米替林治疗纤维肌痛的效果现在在另一项单独评价中论述。阿米替林是一种三环类抗抑郁药,广泛用于治疗慢性神经性疼痛(由神经损伤引起的疼痛)。在许多指南中,它被推荐作为一线治疗药物。低于发挥抗抑郁作用剂量的抗抑郁药物可用于治疗神经性疼痛。

目的

评估阿米替林缓解慢性神经性疼痛的镇痛效果,以及在临床试验中使用该药相关的不良事件。

检索方法

我们检索了截至2015年3月的Cochrane系统评价数据库、MEDLINE和EMBASE,以及两个临床试验注册库,并检索了检索到的论文、之前的系统评价和其他评价的参考文献列表;我们还使用了自己手工检索的数据库来查找较早的研究。

入选标准

我们纳入了至少为期四周的随机、双盲研究,这些研究比较了阿米替林与安慰剂或其他活性治疗药物在慢性神经性疼痛情况下的疗效。

数据收集与分析

我们使用三级证据进行分析。一级证据来自符合当前最佳标准且偏倚风险最小的数据(结果等同于疼痛强度大幅降低,意向性分析不填补失访数据;比较组中至少有200名参与者,为期8至12周,平行设计),二级证据来自未满足上述一项或多项标准且被认为存在一定偏倚风险但比较组中有足够数量参与者的数据,三级证据来自涉及少量参与者的数据,这些数据被认为很可能存在偏倚或使用的是临床效用有限的结局指标,或两者皆有。

主要结果

我们纳入了早期评价中的15项研究和两项新研究(共17项研究,1342名参与者),涉及七种神经性疼痛情况。八项交叉研究共302名参与者,中位数为36名参与者,九项平行组研究共1040名参与者,中位数为84名参与者。研究质量一般,不过由于样本量小,大多数研究存在较高偏倚风险。没有一级或二级证据表明阿米替林对任何神经性疼痛情况有效。只有三级证据。在报告了有效疗效数据的七项研究中,只有两项研究表明阿米替林显著优于安慰剂(证据质量极低)。更多参与者经历了至少一次不良事件;服用阿米替林的参与者中有55%,服用安慰剂的参与者中有36%。风险比(RR)为1.5(95%置信区间(CI)1.3至1.8),额外出现一个有害结局的需治疗人数为5.2(3.6至9.1)(证据质量低)。严重不良事件很少见。不良事件和全因撤药情况无差异,但很少有报告(证据质量极低)。

作者结论

多年来,阿米替林一直是神经性疼痛的一线治疗药物。没有支持其有益效果的无偏倚证据这一事实令人失望,但必须与数十年来许多神经性疼痛患者治疗成功的情况相权衡。没有充分证据表明其无效;相反,我们应该担心的是对治疗效果的高估。阿米替林应继续作为神经性疼痛治疗的一部分使用,但只有少数人能获得满意的疼痛缓解。有限的信息表明,一种抗抑郁药治疗失败并不意味着所有抗抑郁药治疗都会失败。

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