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September 8, 2021BMJ297 citationsOpen Access

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

LWLi WangPHPatrick Jiho HongCMCurtis May

Key Points

  • To evaluate the therapeutic benefits and adverse effects of medical cannabis and cannabinoids for managing chronic non-cancer and cancer-related pain.
  • Systematic search across MEDLINE, EMBASE, CENTRAL, PubMed, and other databases through January 2021 for randomized clinical trials with ≥1 month follow-up.
  • Included 32 randomized controlled trials encompassing 5,174 adult patients with chronic non-cancer pain (n=28) or cancer pain (n=4), evaluating oral (n=30) or topical (n=2) formulations versus placebo (n=29) or non-cannabis controls.
  • Synthesized outcomes using random-effects meta-analyses and evaluated evidence certainty using the GRADE approach.
  • Non-inhaled medical cannabis probably led to a small increase in patients achieving minimally important pain relief (RD 10%, 95% CI 5% to 15%; WMD -0.50 cm on 10 cm VAS, 95% CI -0.75 to -0.25 cm; moderate certainty).
  • Oral cannabis showed very small improvements in physical functioning (RD 4%, 95% CI 0.1% to 8%; WMD 1.67 points, 95% CI 0.03 to 3.31; high certainty) and sleep quality (RD 6%, 95% CI 2% to 9%; WMD -0.35 cm, 95% CI -0.55 to -0.14 cm; high certainty), without improving emotional or social functioning.
  • Oral cannabis increased the risk of transient adverse effects, including drowsiness (RD 5%, 95% CI 2% to 8%), nausea (RD 5%, 95% CI 2% to 8%), and dizziness (RD 9% for <3 months vs. RD 28% for ≥3 months follow-up; P=0.003 for subgroup interaction; high certainty).

Abstract

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 BMJ Rapid Recommendation provides contextualised guidance based on this body of evidence. Systematic review registration https://osf.io/3pwn2

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Wang et al. (2021) studied this question.

synapsesocial.com/papers/6a0cdd34edb32e8d9002626chttps://doi.org/10.1136/bmj.n1034
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