Nury Edris, Schmucker Christine, Nagavci Blin, Motschall Edith, Nitschke Kai, Schulte Erika, Wegwarth Odette, Meerpohl Joerg J
Institute for Evidence in Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Institute of Medical Biometry and Statistics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Pain. 2022 Apr 1;163(4):610-636. doi: 10.1097/j.pain.0000000000002423.
In recent years, long-term prescribing and use of strong opioids for chronic noncancer pain (CNCP) has increased in high-income countries. Yet existing uncertainties, controversies, and differing recommendations make the rationale for prolonged opioid use in CNCP unclear. This systematic review and meta-analyses compared the efficacy, safety, and tolerability of strong opioids with placebo or nonopioid therapy in CNCP, with a special focus on chronic low back pain (CLBP). Systematic literature searches were performed in 4 electronic databases (MEDLINE, Web of Science, Cochrane Library, and CINAHL) in July 2019 and updated by regular alerts until December 2020. We included 16 placebo-controlled randomized controlled trials for CLBP and 5 studies (2 randomized controlled trials and 3 nonrandomized studies) of opioids vs nonopioids for CNCP in the quantitative and qualitative synthesis. Random effects pairwise meta-analyses were performed for efficacy, safety, and tolerability outcomes and subgroup analyses for treatment duration, study design, and opioid experience status. Very low to low certainty findings suggest that 4 to 15 weeks (short or intermediate term) opioid therapy in CLBP (compared with placebo) may cause clinically relevant reductions in pain but also more gastrointestinal and nervous system adverse events, with likely no effect on disability. By contrast, long-term opioid therapy (≥6 months) in CNCP may not be superior to nonopioids in improving pain or disability or pain-related function but seems to be associated with more adverse events, opioid abuse or dependence, and possibly an increase in all-cause mortality. Our findings also underline the importance and need for well-designed trials assessing long-term efficacy and safety of opioids for CNCP and CLBP.
近年来,高收入国家中用于慢性非癌性疼痛(CNCP)的强效阿片类药物的长期处方和使用有所增加。然而,现有的不确定性、争议以及不同的建议使得在CNCP中延长使用阿片类药物的理由尚不清楚。本系统评价和荟萃分析比较了强效阿片类药物与安慰剂或非阿片类疗法在CNCP中的疗效、安全性和耐受性,特别关注慢性下腰痛(CLBP)。2019年7月在4个电子数据库(MEDLINE、科学网、Cochrane图书馆和CINAHL)中进行了系统的文献检索,并通过定期提醒进行更新,直至2020年12月。在定量和定性综合分析中,我们纳入了16项针对CLBP的安慰剂对照随机对照试验,以及5项关于阿片类药物与非阿片类药物治疗CNCP的研究(2项随机对照试验和3项非随机研究)。对疗效、安全性和耐受性结果进行了随机效应成对荟萃分析,并对治疗持续时间、研究设计和阿片类药物使用经验状态进行了亚组分析。极低至低确定性的研究结果表明,CLBP中4至15周(短期或中期)的阿片类药物治疗(与安慰剂相比)可能会在临床上显著减轻疼痛,但也会导致更多的胃肠道和神经系统不良事件,对残疾可能没有影响。相比之下,CNCP中的长期阿片类药物治疗(≥6个月)在改善疼痛、残疾或疼痛相关功能方面可能并不优于非阿片类药物,但似乎与更多的不良事件、阿片类药物滥用或依赖有关,并且可能会增加全因死亡率。我们的研究结果还强调了设计良好的试验评估阿片类药物对CNCP和CLBP的长期疗效和安全性的重要性和必要性。