George Institute for Global Health, University of Sydney, PO Box M201, Camperdown, Sydney, NSW 2050, Australia.
BMJ. 2012 Feb 13;344:e497. doi: 10.1136/bmj.e497.
To investigate the efficacy and tolerability of analgesic and adjuvant pain drugs typically administered in primary care for the management of patients with sciatica.
Systematic review. Data source International Pharmaceutical Abstracts, PsycINFO, Medline, Embase, Cochrane Central Register of Clinical Trials (CENTRAL), CINAHL, and LILACS.
Randomised controlled trials assessing the efficacy and tolerability of drugs versus placebo or other treatment for sciatica.
Two independent reviewers extracted data and assessed methodological quality using the PEDro scale. Pain and disability outcomes were converted to a common 0 to 100 scale. Data were pooled with a random effects model, and the GRADE approach was used in summary conclusions.
Twenty three published reports met the inclusion criteria. The evidence to judge the efficacy of non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, antidepressants, anticonvulsants, muscle relaxants, and opioid analgesics ranged from moderate to low quality. Most of the pooled estimates did not favour the active treatment over placebo. The pooled results of two trials of corticosteroids (mean difference in overall and leg pain -12.2, 95% confidence interval -20.9 to -3.4) and a single trial of the anticonvulsant gabapentin for chronic sciatica (mean difference in overall pain relief -26.6, -38.3 to -14.9) showed some benefits but only in the short term. The median rate of adverse events was 17% (interquartile range 10-30%) for the active drugs and 11% (3-23%) for placebo. Trial limitations included failure to use validated outcome measures, lack of long term follow-up, and small sample size.
As the existing evidence from clinical trials is of low quality, the efficacy and tolerability of drugs commonly prescribed for the management of sciatica in primary care is unclear.
调查在初级保健中用于治疗坐骨神经痛患者的典型镇痛和辅助止痛药物的疗效和耐受性。
系统评价。资料来源:国际药学文摘、PsycINFO、Medline、Embase、Cochrane 临床对照试验中心注册库(CENTRAL)、CINAHL 和 LILACS。
评估药物与安慰剂或其他治疗方法治疗坐骨神经痛的疗效和耐受性的随机对照试验。
两名独立的综述作者使用 PEDro 量表提取数据并评估方法学质量。疼痛和残疾结局转换为通用的 0 到 100 量表。使用随机效应模型对数据进行汇总,并使用 GRADE 方法得出总结结论。
符合纳入标准的 23 项已发表报告。判断非甾体抗炎药(NSAIDs)、皮质类固醇、抗抑郁药、抗惊厥药、肌肉松弛剂和阿片类镇痛药疗效的证据质量从中等到低不等。大多数汇总估计并不支持活性治疗优于安慰剂。两项皮质类固醇试验(总疼痛和腿部疼痛的汇总差异 -12.2,95%置信区间 -20.9 至 -3.4)和一项单发性抗惊厥药加巴喷丁治疗慢性坐骨神经痛的试验(总疼痛缓解的汇总差异 -26.6,-38.3 至 -14.9)的结果显示出一些益处,但仅在短期内如此。活性药物的不良反应发生率中位数为 17%(四分位距 10-30%),安慰剂为 11%(3-23%)。试验局限性包括未使用验证后的结局测量、缺乏长期随访以及样本量小。
由于现有临床试验证据质量较低,因此在初级保健中常用于治疗坐骨神经痛的药物的疗效和耐受性尚不清楚。