Sydney Musculoskeletal Health, Institute for Musculoskeletal Health, The University of Sydney and Sydney Local Health District, Sydney, Australia.
, Level 10N KGV Building, Missenden Road, Camperdown, NSW, 2050, Australia.
Drugs. 2024 Mar;84(3):305-317. doi: 10.1007/s40265-024-01999-5. Epub 2024 Mar 7.
To evaluate the efficacy of opioids for people with acute musculoskeletal pain against placebo.
Systematic review and meta-analyses of randomised, placebo-controlled trials of opioid analgesics for acute musculoskeletal pain in any setting. The primary outcomes were pain and disability at the immediate timepoint (< 24 h).
Multiple databases were searched from their inception to February 22nd, 2023.
Continuous outcomes were converted to a 0-100 scale. Dichotomous outcomes were presented as risk differences. Risk of bias and certainty of evidence was assessed.
We located 17 trials (1 intravenous and 16 oral route of administration). For adults, high certainty evidence from 11 comparisons shows that oral opioids provide small benefits relative to placebo in the immediate term for pain (mean difference [MD] - 8.8 95% confidence interval [CI] - 12.0 to - 5.6). For disability, the difference is uncertain (MD - 6.2, 95% CI - 17.8 to 5.4). Opioid groups were at higher risk of adverse events (MD 14.3%, 95% CI 8.3-20.4%, very low certainty). There was moderate certainty evidence of a large effect of IV morphine on sciatica pain (MD -42.5, 95% CI - 49.9 to - 35.1, n = 197, 1 study). In paediatric populations, moderate certainty evidence from 3 trials shows that oral opioids probably do not provide benefit beyond that of placebo for pain (MD 6.1, 95% CI - 1.7 to 12.8) and there was no evidence for disability. There was low certainty evidence that there may be no difference in adverse events (MD 10.4%, 95% CI - 0.6 to 21.4%).
Intravenous morphine likely offers benefits, but oral opioids may not provide clinically meaningful benefits.
CRD42021249346.
评估阿片类药物治疗急性肌肉骨骼疼痛的疗效,与安慰剂相比。
系统评价和荟萃分析,针对任何环境下阿片类镇痛药治疗急性肌肉骨骼疼痛的随机、安慰剂对照试验。主要结局为即刻(<24 小时)的疼痛和残疾。
从数据库创建开始到 2023 年 2 月 22 日,对多个数据库进行了搜索。
将连续结果转换为 0-100 刻度。二分类结果表示为风险差异。评估了偏倚风险和证据确定性。
我们找到了 17 项试验(1 项静脉内和 16 项口服途径)。对于成年人,11 项比较的高确定性证据表明,与安慰剂相比,口服阿片类药物在即时期对疼痛有较小的益处(平均差异 [MD] -8.8,95%置信区间 [CI] -12.0 至 -5.6)。对于残疾,差异不确定(MD -6.2,95% CI -17.8 至 5.4)。阿片类药物组发生不良反应的风险更高(MD 14.3%,95% CI 8.3-20.4%,极低确定性)。有中等确定性证据表明静脉内吗啡对坐骨神经痛疼痛有很大影响(MD -42.5,95% CI -49.9 至 -35.1,n = 197,1 项研究)。在儿科人群中,3 项试验的中等确定性证据表明,口服阿片类药物对疼痛的疗效可能并不优于安慰剂(MD 6.1,95% CI -1.7 至 12.8),且无残疾证据。有低确定性证据表明,不良反应可能没有差异(MD 10.4%,95% CI -0.6 至 21.4%)。
静脉内吗啡可能有好处,但口服阿片类药物可能没有提供临床有意义的益处。
CRD42021249346。