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系统评价局部外用双氯芬酸治疗急慢性肌肉骨骼疼痛。

Systematic review of topical diclofenac for the treatment of acute and chronic musculoskeletal pain.

机构信息

Pain Research Unit, Churchill Hospital, Oxford University Hospitals, Oxford, UK.

The Nottingham China Health Institute, The University of Nottingham Ningbo, Ningbo, Zhejiang, China.

出版信息

Curr Med Res Opin. 2020 Apr;36(4):637-650. doi: 10.1080/03007995.2020.1716703. Epub 2020 Feb 3.

Abstract

The objective was to systematically review the efficacy and safety of topical diclofenac in both acute and chronic musculoskeletal pain in adults. We used standard Cochrane methods. Searches were conducted in MEDLINE, EMBASE and The Cochrane Register of Studies; date of the final search was November 2018. Included studies were randomized, double blinded, with ten or more participants per treatment arm. The primary outcome of "clinical success" was defined as participant-reported reduction in pain of at least 50%. Details of adverse events (AEs) were recorded. For acute pain, 23 studies (5170 participants) were included. Compared to placebo, number needed to treat (NNT) for different formulations were as follows: diclofenac plaster, 4.7 (95% CI 3.7-6.5); diclofenac plaster with heparin, 7.4 (95% CI 4.6-19); and diclofenac Emulgel, 1.8 (95% CI 1.5-2.1). 4.1% (78/1919) reported a local AE. For chronic pain, 21 studies (26 publications) with 5995 participants were included. Formulations included gel, solution with or without DMSO, emulsion and plaster. A clinical success rate of ∼60% (NNT 9.5 [95% CI 7-14.7]) was achieved with a variety of formulations. Local AEs (∼14%) were similar for both diclofenac and placebo. This systematic review of 11,000+ participants demonstrates that topical diclofenac is effective for acute pain, such as sprains, with minimal AEs. The effectiveness of topical diclofenac was also demonstrated in chronic musculoskeletal pain but with a higher NNT (worse) compared with acute pain. Formulation does play a part in effectiveness but needs further studies.

摘要

目的

系统评价双氯芬酸局部制剂治疗成人急性和慢性肌肉骨骼疼痛的疗效和安全性。我们使用标准的 Cochrane 方法。在 MEDLINE、EMBASE 和 Cochrane 对照试验注册库中进行检索;最后一次检索日期为 2018 年 11 月。纳入的研究为随机、双盲,每组至少 10 名参与者。主要结局指标为“临床疗效”,定义为患者报告的疼痛减轻至少 50%。记录不良事件(AE)的详细信息。对于急性疼痛,纳入 23 项研究(5170 名参与者)。与安慰剂相比,不同制剂的治疗需要人数(NNT)如下:双氯芬酸贴剂,4.7(95%CI 3.7-6.5);含肝素的双氯芬酸贴剂,7.4(95%CI 4.6-19);双氯芬酸 Emulgel,1.8(95%CI 1.5-2.1)。4.1%(78/1919)报告有局部 AE。对于慢性疼痛,纳入 21 项研究(26 篇文献),5995 名参与者。制剂包括凝胶、含或不含 DMSO 的溶液、乳剂和贴剂。多种制剂的临床疗效率约为 60%(NNT 9.5[95%CI 7-14.7])。双氯芬酸和安慰剂的局部 AE(约 14%)相似。这项纳入 11000 多名参与者的系统评价表明,双氯芬酸局部制剂治疗急性疼痛(如扭伤)有效,不良反应较少。双氯芬酸在慢性肌肉骨骼疼痛中也有效,但与急性疼痛相比,NNT(更差)更高。制剂确实在疗效中起作用,但需要进一步研究。

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