Professor of Evidence-Based Medicine in the Department of Family Medicine at the University of Alberta in Edmonton.
Knowledge Translation Expert in the Physician Learning Program with the Alberta Medical Association and in Lifelong Learning and the Department of Family Medicine at the University of Alberta.
Can Fam Physician. 2018 Feb;64(2):e78-e94.
To determine the effects of medical cannabinoids on pain, spasticity, and nausea and vomiting, and to identify adverse events.
MEDLINE, the Cochrane Database, and the references of included studies were searched.
Systematic reviews with 2 or more randomized controlled trials (RCTs) that focused on medical cannabinoids for pain, spasticity, or nausea and vomiting were included. For adverse events, any meta-analysis for the conditions listed or of adverse events of cannabinoids was included.
From 1085 articles, 31 relevant systematic reviews were identified including 23 for pain, 5 for spasticity, 6 for nausea and vomiting, and 12 for adverse events. Meta-analysis of 15 RCTs found more patients taking cannabinoids attained at least a 30% pain reduction: risk ratio (RR) of 1.37 (95% CI 1.14 to 1.64), number needed to treat (NNT) of 11. Sensitivity analysis found study size and duration affected findings (subgroup differences, ≤ .03), with larger and longer RCTs finding no benefit. Meta-analysis of 4 RCTs found a positive global impression of change in spasticity (RR = 1.45, 95% CI 1.08 to 1.95, NNT = 7). Other results were not consistently statistically significant, but when positive, a 30% or more improvement in spasticity had an NNT of 10. Meta-analysis of 7 RCTs for control of nausea and vomiting after chemotherapy found an RR of 3.60 (95% CI 2.55 to 5.09) with an NNT of 3. Adverse effects caused more patients to stop treatment (number needed to harm [NNH] of 8 to 22). Individual adverse events were very common, including dizziness (NNH = 5), sedation (NNH = 5), confusion (NNH = 15), and dissociation (NNH = 20). "Feeling high" was reported in 35% to 70% of users. The GRADE (Grading of Recommendations Assessment, Development and Evaluation) evaluation reduced evidence ratings of benefit to low or very low.
There is reasonable evidence that cannabinoids improve nausea and vomiting after chemotherapy. They might improve spasticity (primarily in multiple sclerosis). There is some uncertainty about whether cannabinoids improve pain, but if they do, it is neuropathic pain and the benefit is likely small. Adverse effects are very common, meaning benefits would need to be considerable to warrant trials of therapy.
确定医用大麻素对疼痛、痉挛和恶心呕吐的影响,并确定不良反应。
检索了 MEDLINE、Cochrane 数据库和纳入研究的参考文献。
纳入了 2 项或 2 项以上随机对照试验 (RCT) 系统评价,重点关注医用大麻素治疗疼痛、痉挛或恶心呕吐。对于不良反应,纳入了针对所列疾病或大麻素不良反应的任何荟萃分析。
从 1085 篇文章中,确定了 31 篇相关的系统评价,其中 23 篇用于疼痛,5 篇用于痉挛,6 篇用于恶心呕吐,12 篇用于不良反应。对 15 项 RCT 的荟萃分析发现,更多接受大麻素治疗的患者疼痛至少减轻 30%:风险比 (RR) 为 1.37(95%置信区间 1.14 至 1.64),需要治疗的人数 (NNT) 为 11。敏感性分析发现研究规模和持续时间影响研究结果(亚组差异, ≤.03),较大和较长时间的 RCT 发现没有益处。对 4 项 RCT 的荟萃分析发现,痉挛的整体印象改善有统计学意义(RR = 1.45,95%置信区间 1.08 至 1.95,NNT = 7)。其他结果没有统计学意义,但当痉挛改善 30%或更多时,NNT 为 10。对 7 项 RCT 用于化疗后控制恶心呕吐的荟萃分析发现,RR 为 3.60(95%置信区间 2.55 至 5.09),NNT 为 3。不良反应导致更多患者停止治疗(危害人数需要 [NNH] 为 8 至 22)。个别不良反应非常常见,包括头晕(NNH = 5)、镇静(NNH = 5)、意识模糊(NNH = 15)和分离(NNH = 20)。35%至 70%的使用者报告“感觉兴奋”。GRADE(推荐评估、制定与评价)评估将受益的证据等级降低至低或极低。
有合理的证据表明大麻素可改善化疗后的恶心呕吐。它们可能改善痉挛(主要在多发性硬化症中)。关于大麻素是否改善疼痛尚不确定,但如果有,那就是神经性疼痛,而且益处可能很小。不良反应非常常见,这意味着治疗益处需要相当大才能进行试验。