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Treatment of fibromyalgia syndrome with gabapentin and pregabalin--a meta-analysis of randomized controlled trials.

机译:加巴喷丁和普瑞巴林治疗纤维肌痛综合征的随机对照试验的荟萃分析。

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The efficacy of gabapentin (GPT) and pregabalin (PGB) in the treatment of fibromyalgia syndrome (FMS) was assessed. We screened MEDLINE, PsycINFO, SCOPUS, www.clinicaltrials.org, the Cochrane Library (through October 2008), and the reference sections of original studies on GPT/PGB in FMS. Randomized controlled trials (RCTs) on the treatment of FMS with GPT and PGB were analyzed. Six out of 127 RCTs studying 2422 subjects on treatment with GPT (one study) or PGB (five studies) and 1056 subjects on placebo with a median treatment duration of 11 weeks were included into the systematic review. Five studies were suitable for meta-analysis. Effects were summarized using standardized mean differences (SMD). There was strong evidence for a reduction of pain (SMD -0.28, 95% CI -0.36, -0.20; p<0.001), improved sleep (SMD -0.39, 95% CI -0.48, -0.39; p<0.001), and improved health-related quality of life (HRQOL) (SMD -0.30, 95% CI -0.46, -0.15; p<0.001), but not for depressed mood (SMD -0.12, 95% CI -0.30, 0.06; p=0.18). There was strong evidence for a non-substantial reduction of fatigue (SMD -0.16, 95% CI -0.23, -0.09, p<0.001) and of anxiety (SMD -0.18, 95% CI -0.27, -0.10; p<0.001). The external validity of the studies was limited because patients with severe somatic and mental disorders were excluded.
机译:评估了加巴喷丁(GPT)和普瑞巴林(PGB)在治疗纤维肌痛综合征(FMS)中的功效。我们筛选了MEDLINE,PsycINFO,SCOPUS,www.clinicaltrials.org,Cochrane图书馆(截止到2008年10月)以及FMS中有关GPT / PGB的原始研究的参考部分。分析了使用GPT和PGB治疗FMS的随机对照试验(RCT)。在127个RCT中,有6个研究了2422名接受GPT(一项研究)或PGB(五项研究)治疗的受试者和1056名接受安慰剂的受试者,中位治疗时间为11周。有五项研究适合进行荟萃分析。使用标准化均值差(SMD)总结效果。有强有力的证据表明疼痛减轻(SMD -0.28,95%CI -0.36,-0.20; p <0.001),睡眠改善(SMD -0.39,95%CI -0.48,-0.39; p <0.001),和改善与健康有关的生活质量(HRQOL)(SMD -0.30,95%CI -0.46,-0.15; p <0.001),但不适用于情绪低落(SMD -0.12,95%CI -0.30,0.06; p = 0.18 )。有强有力的证据表明疲劳(SMD -0.16,95%CI -0.23,-0.09,p <0.001)和焦虑症(SMD -0.18,95%CI -0.27,-0.10; p <0.001 )。由于排除了患有严重躯体和精神疾病的患者,研究的外部有效性有限。

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