Suppr超能文献

医学大麻或大麻素治疗慢性非癌症和癌症相关疼痛:随机临床试验的系统评价和荟萃分析。

Medical cannabis or cannabinoids for chronic non-cancer and cancer related pain: a systematic review and meta-analysis of randomised clinical trials.

机构信息

Department of Anesthesia, McMaster University, Hamilton, Ontario, Canada

The Michael G. DeGroote Institute for Pain Research and Care, McMaster University, Hamilton, Ontario, Canada.

出版信息

BMJ. 2021 Sep 8;374:n1034. doi: 10.1136/bmj.n1034.

Abstract

OBJECTIVE

To determine the benefits and harms of medical cannabis and cannabinoids for chronic pain.

DESIGN

Systematic review and meta-analysis.

DATA SOURCES

MEDLINE, EMBASE, AMED, PsycInfo, CENTRAL, CINAHL, PubMed, Web of Science, Cannabis-Med, Epistemonikos, and trial registries up to January 2021.

STUDY SELECTION

Randomised clinical trials of medical cannabis or cannabinoids versus any non-cannabis control for chronic pain at ≥1 month follow-up.

DATA EXTRACTION AND SYNTHESIS

Paired reviewers independently assessed risk of bias and extracted data. We performed random-effects models meta-analyses and used GRADE to assess the certainty of evidence.

RESULTS

A total of 32 trials with 5174 adult patients were included, 29 of which compared medical cannabis or cannabinoids with placebo. Medical cannabis was administered orally (n=30) or topically (n=2). Clinical populations included chronic non-cancer pain (n=28) and cancer related pain (n=4). Length of follow-up ranged from 1 to 5.5 months. Compared with placebo, non-inhaled medical cannabis probably results in a small increase in the proportion of patients experiencing at least the minimally important difference (MID) of 1 cm (on a 10 cm visual analogue scale (VAS)) in pain relief (modelled risk difference (RD) of 10% (95% confidence interval 5% to 15%), based on a weighted mean difference (WMD) of -0.50 cm (95% CI -0.75 to -0.25 cm, moderate certainty)). Medical cannabis taken orally results in a very small improvement in physical functioning (4% modelled RD (0.1% to 8%) for achieving at least the MID of 10 points on the 100-point SF-36 physical functioning scale, WMD of 1.67 points (0.03 to 3.31, high certainty)), and a small improvement in sleep quality (6% modelled RD (2% to 9%) for achieving at least the MID of 1 cm on a 10 cm VAS, WMD of -0.35 cm (-0.55 to -0.14 cm, high certainty)). Medical cannabis taken orally does not improve emotional, role, or social functioning (high certainty). Moderate certainty evidence shows that medical cannabis taken orally probably results in a small increased risk of transient cognitive impairment (RD 2% (0.1% to 6%)), vomiting (RD 3% (0.4% to 6%)), drowsiness (RD 5% (2% to 8%)), impaired attention (RD 3% (1% to 8%)), and nausea (RD 5% (2% to 8%)), but not diarrhoea; while high certainty evidence shows greater increased risk of dizziness (RD 9% (5% to 14%)) for trials with <3 months follow-up versus RD 28% (18% to 43%) for trials with ≥3 months follow-up; interaction test P=0.003; moderate credibility of subgroup effect).

CONCLUSIONS

Moderate to high certainty evidence shows that non-inhaled medical cannabis or cannabinoids results in a small to very small improvement in pain relief, physical functioning, and sleep quality among patients with chronic pain, along with several transient adverse side effects, compared with placebo. The accompanying Rapid Recommendation provides contextualised guidance based on this body of evidence. SYSTEMATIC REVIEW REGISTRATION: https://osf.io/3pwn2.

摘要

目的

确定医用大麻和大麻素治疗慢性疼痛的益处和危害。

设计

系统评价和荟萃分析。

数据来源

MEDLINE、EMBASE、AMED、PsycInfo、CENTRAL、CINAHL、PubMed、Web of Science、Cannabis-Med、Epistemonikos 和试验注册处,截至 2021 年 1 月。

研究选择

至少有 1 个月随访的医用大麻或大麻素与任何非大麻对照治疗慢性疼痛的随机临床试验。

数据提取和综合

配对审查员独立评估偏倚风险并提取数据。我们进行了随机效应模型荟萃分析,并使用 GRADE 评估证据的确定性。

结果

共纳入了 32 项试验,涉及 5174 名成年患者,其中 29 项比较了医用大麻或大麻素与安慰剂。医用大麻经口服(n=30)或局部使用(n=2)。临床人群包括慢性非癌性疼痛(n=28)和癌症相关疼痛(n=4)。随访时间从 1 到 5.5 个月不等。与安慰剂相比,非吸入性医用大麻可能会使至少达到 1 厘米最小重要差异(MID)的患者比例略有增加(疼痛缓解的模型风险差异(RD)为 10%(95%置信区间为 5%至 15%),基于加权平均差异(WMD)为-0.50cm(95%CI-0.75 至-0.25cm,中等确定性))。口服医用大麻对身体功能有很小的改善(达到至少 100 点 SF-36 身体功能量表的 10 分 MID 的 4%模型 RD(0.1%至 8%),WMD 为 1.67 分(0.03 至 3.31,高确定性)),对睡眠质量的改善也很小(达到至少 10cm VAS 1cm MID 的 6%模型 RD(2%至 9%),WMD 为-0.35cm(-0.55 至-0.14cm,高确定性))。口服医用大麻不能改善情感、角色或社会功能(高确定性)。中等确定性证据表明,口服医用大麻可能会导致短暂认知障碍的风险略有增加(RD 2%(0.1%至 6%))、呕吐(RD 3%(0.4%至 6%))、嗜睡(RD 5%(2%至 8%))、注意力受损(RD 3%(1%至 8%))和恶心(RD 5%(2%至 8%)),但不会腹泻;而高确定性证据表明,与随访时间≥3 个月的试验相比,随访时间<3 个月的试验中头晕的风险增加(RD 9%(5%至 14%)),而随访时间≥3 个月的试验中头晕的风险增加(RD 28%(18%至 43%));交互检验 P=0.003;亚组效应可信度中等)。

结论

中等至高确定性证据表明,与安慰剂相比,非吸入性医用大麻或大麻素可使慢性疼痛患者的疼痛缓解、身体功能和睡眠质量略有至非常小的改善,同时伴有一些短暂的不良反应。快速推荐提供了基于该证据的背景化指导。系统评价注册:https://osf.io/3pwn2。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验