Martinez Valeria, Pichard Xavier, Fletcher Dominique
Service d'anesthésie, Hôpital Raymond Poincaré, Garches, Assistance Publique Hôpitaux de Paris, France.
INSERM, U-987, Hôpital Ambroise Paré, Centre d'Evaluation et de Traitement de la Douleur, Boulogne-Billancourt, France.
Pain. 2017 May;158(5):775-783. doi: 10.1097/j.pain.0000000000000838.
The efficacy of perioperative pregabalin treatment for preventing chronic pain remains a matter of debate. We searched the MEDLINE, EMBASE, LILACS, Cochrane, and Clinical Trial Register databases, and other sources, for randomized controlled trials comparing the effects of pregabalin and placebo. The primary outcome was the incidence of chronic postsurgical pain (CPSP) at 3 months. The secondary endpoints were CPSP at 3, 6, and 12 months and the incidence of chronic postsurgical neuropathic pain at the same time points. A random-effect meta-analysis was performed on the combined data. Evidence quality was rated by the GRADE method. We included 18 studies (2485 patients) in the meta-analysis. Overall, 60% of the trials reporting the primary outcome at 3 months were unpublished; the unpublished trials corresponded to 1492/1884 (79%) of the patients included in these studies. No difference in CPSP incidence between pregabalin and placebo was found at any time point; the risk ratio was 0.87 (0.66, 1.14), I = 57% at 3 months. The evidence was considered to be of moderate quality. Subgroup analysis by publication status, daily dose, type of administration, and type of surgery did not highlight any differences between subgroups. Insufficient data concerning the incidence of chronic postsurgical neuropathic pain were available for any firm recommendation to be made. Pooled data from published and unpublished studies provide no support for the efficacy of pregabalin for preventing CPSP.
围手术期使用普瑞巴林预防慢性疼痛的疗效仍存在争议。我们检索了MEDLINE、EMBASE、LILACS、Cochrane和临床试验注册数据库以及其他来源,以查找比较普瑞巴林和安慰剂效果的随机对照试验。主要结局是术后3个月慢性术后疼痛(CPSP)的发生率。次要终点是3、6和12个月时的CPSP以及相同时间点慢性术后神经性疼痛的发生率。对合并数据进行随机效应荟萃分析。证据质量采用GRADE方法进行评级。我们在荟萃分析中纳入了18项研究(2485例患者)。总体而言,报告3个月主要结局的试验中有60%未发表;未发表的试验对应于这些研究中纳入患者的1492/1884(79%)。在任何时间点,普瑞巴林和安慰剂之间的CPSP发生率均未发现差异;3个月时风险比为0.87(0.66,1.14);I² = 57%。证据被认为质量中等。按发表状态、每日剂量、给药类型和手术类型进行的亚组分析未突出亚组之间的任何差异。关于慢性术后神经性疼痛发生率的数据不足,无法做出任何确切的推荐。来自已发表和未发表研究的汇总数据不支持普瑞巴林预防CPSP的疗效。