Study register · detailMeta-Analyse · Opioid Reduction · 2022
Opioid-sparing effect of cannabinoids for analgesia: an updated systematic review and meta-analysis of preclinical and clinical studies
Nielsen et al.·NeuropsychopharmacologyImpact 4.4
MixedGRADEHigh87 citations
Samplek = 92 Studien
Duration2016 onwards
ControlOpioids alone or placebo
EndpointOpioid dose requirement /…
Blindingn.a.
DesignMeta-Analyse
”Key finding
Preclinical and observational studies show potential opioid-sparing effects of cannabinoids, while higher-quality RCTs show no evidence for opioid-sparing effects.
Summary
Comprehensive SR+MA on opioid-sparing effects of cannabinoids (k=92 studies including 15 ongoing trials). Preclinical: ED50 of morphine+THC 3.5-fold lower than morphine alone (95% CI 2.04-6.03). Clinical-acute: 3 RCTs found no opioid sparing in acute pain. Cancer pain: k=4 RCTs, no reduction in opioid dose (MD -3.8 mg, 95% CI -10.97 to 3.37) or pain scores (MD 1.84, 95% CI -2.05 to 5.72); more adverse events vs. placebo (RR 1.13, 95% CI 1.03-1.24). Chronic non-cancer pain: 3 RCTs without dronabinol effect. Observational studies: 39% reported opioid discontinuation (95% CI 0.15-0.64), 85% reduction (95% CI 0.64-0.99). Preclinical/observational data suggesting potential, RCT evidence contradictory.
P
PopulationPreclinical models as well as patients with acute pain, cancer pain and chronic non-tumour pain – pooled sample variable across studies
I
InterventionCannabinoids (including THC, dronabinol) as co-administration to opioids
C
ControlOpioids alone or placebo
O
OutcomePreclinical: ED50 morphine 3,5-fold lower with THC (95% CI 2,04–6,03); RCTs cancer pain: no opioid-sparing effect (MD –3,8 mg, 95% CI –10,97 to 3,37); observational studies: 39% opioid discontinuation, 85% opioid reduction
Confidence in the evidence
Very lowLowModerateHigh
High
The highest of four GRADE levels, the effect estimate is very reliable.
Cannabinoid co-administration may enable reduced opioid doses for analgesia. This updated systematic review on the opioid-sparing effects of cannabinoids considered preclinical and clinical studies where the outcome was analgesia or opioid dose requirements. We searched Scopus, Cochrane Central Registry of Controlled Trials, Medline, and Embase (2016 onwards). Ninety-two studies met the search criteria including 15 ongoing trials. Meta-analysis of seven preclinical studies found the median effective dose (ED(50)) of morphine administered with delta-9-tetrahydrocannabinol was 3.5 times lower (95% CI 2.04, 6.03) than the ED(50) of morphine alone. Six preclinical studies found no evidence of increased opioid abuse liability with cannabinoid administration. Of five healthy-volunteer experimental pain studies, two found increased pain, two found decreased pain and one found reduced pain bothersomeness with cannabinoid administration; three demonstrated that cannabinoid co-administration may increase opioid abuse liability. Three randomized controlled trials (RCTs) found no evidence of opioid-sparing effects of cannabinoids in acute pain. Meta-analysis of four RCTs in patients with cancer pain found no effect of cannabinoid administration on opioid dose (mean difference -3.8 mg, 95% CI -10.97, 3.37) or percentage change in pain scores (mean difference 1.84, 95% CI -2.05, 5.72); five studies found more adverse events with cannabinoids compared with placebo (risk ratio 1.13, 95% CI 1.03, 1.24). Of five controlled chronic non-cancer pain trials; one low-quality study with no control arm, and one single-dose study reported reduced pain scores with cannabinoids. Three RCTs found no treatment effect of dronabinol. Meta-analyses of observational studies found 39% reported opioid cessation (95% CI 0.15, 0.64, I(2) 95.5%, eight studies), and 85% reported reduction (95% CI 0.64, 0.99, I(2) 92.8%, seven studies). In summary, preclinical and observational studies demonstrate the potential opioid-sparing effects of cannabinoids in the context of analgesia, in contrast to higher-quality RCTs that did not provide evidence of opioid-sparing effects.