Study register · detail
Mixed
GRADE
High
46 citations
Samplek = 46 Studien
n = 6.216 Pat.
n = 6.216 Pat.
DurationJanuary 1, 1990 to October 3…
ControlPlacebo/control groups
EndpointAdverse events
Blindingdoppelblind
DesignSystematische Review + Meta-Analyse
Key finding
THC-containing cannabinoids significantly increase the rate of adverse events in older adults, but are not more dangerous than controls with regard to serious AEs and deaths; CBD alone appears safe.
Summary
SR+MA, k=46 RCTs, n=6.216 adults ≥50 years; THC-containing CBMs significantly increased all AEs: THC alone IRR 1,42 [95% CI 1,12–1,78]; THC:CBD combination IRR 1,58 [95% CI 1,26–1,98]; THC:CBD increased discontinuation rate due to AEs (RR 1,40 [95% CI 1,08–1,80]); no significantly increased risk for serious AEs or deaths; CBD alone: IRR 1,02 [95% CI 0,90–1,16], no increased AE risk.
P
PopulationAdults ≥50 years (mean age 58,6 ± 7,5 years) with various indications, pooled n=6.216, of which 3.469 under CBM
I
InterventionNatural and synthetic cannabinoid-based medicines (THC alone, THC:CBD combination, CBD alone)
C
ControlPlacebo/control groups
O
OutcomeTHC-containing CBM significantly increased all adverse events (AEs): THC alone IRR 1,42 (95% CI 1,12–1,78), THC:CBD IRR 1,58 (95% CI 1,26–1,98); SAEs and deaths not significantly increased; CBD alone no significant increase in AEs (IRR 1,02, 95% CI 0,90–1,16)
Confidence in the evidence
High
The highest of four GRADE levels, the effect estimate is very reliable.
Quality profile
Sample size
★★★★★
Blinding
Double-blind
Effect size
Mixed
Citations / year
★★★★★
Authors
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Abstract
<h4>Background</h4>Cannabinoid-based medicines (CBMs) are being used widely in the elderly. However, their safety and tolerability in older adults remains unclear. We aimed to conduct a systematic review and meta-analysis of safety and tolerability of CBMs in adults of age ≥50 years.<h4>Methods and findings</h4>A systematic search was performed using MEDLINE, PubMed, EMBASE, CINAHL PsychInfo, Cochrane Library, and ClinicalTrials.gov (1 January 1990 to 3 October 2020). Randomised clinical trials (RCTs) of CBMs in those with mean age of ≥50 years for all indications, evaluating the safety/tolerability of CBMs where adverse events have been quantified, were included. Study quality was assessed using the GRADE (Grading of Recommendations Assessment, Development, and Evaluation) criteria and Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines were followed. Two reviewers conducted all review stages independently. Where possible, data were pooled using random-effects meta-analysis. Effect sizes were calculated as incident rate ratio (IRR) for outcome data such as adverse events (AEs), serious AEs (SAEs), and death and risk ratio (RR) for withdrawal from study and reported separately for studies using tetrahydrocannabinol (THC), THC:cannabidiol (CBD) combination, and CBD. A total of 46 RCTs were identified as suitable for inclusion of which 31 (67%) were conducted in the United Kingdom and Europe. There were 6,216 patients (mean age 58.6 ± 7.5 years; 51% male) included in the analysis, with 3,469 receiving CBMs. Compared with controls, delta-9-tetrahydrocannabinol (THC)-containing CBMs significantly increased the incidence of all-cause and treatment-related AEs: THC alone (IRR: 1.42 [95% CI, 1.12 to 1.78]) and (IRR: 1.60 [95% CI,1.26 to 2.04]); THC:CBD combination (IRR: 1.58 [95% CI,1.26 to 1.98]) and (IRR: 1.70 [95% CI,1.24 to 2.33]), respectively. IRRs of SAEs and deaths were not significantly greater under CBMs containing THC with or without CBD. THC:CBD combination (RR: 1.40 [95% CI, 1.08 to 1.80]) but not THC alone (RR: 1.18 [95% CI, 0.89 to 1.57]) significantly increased risk of AE-related withdrawals. CBD alone did not increase the incidence of all-cause AEs (IRR: 1.02 [95% CI, 0.90 to 1.16]) or other outcomes as per qualitative synthesis. AE-related withdrawals were significantly associated with THC dose in THC only [QM (df = 1) = 4.696, p = 0.03] and THC:CBD combination treatment ([QM (df = 1) = 4.554, p = 0.033]. THC-containing CBMs significantly increased incidence of dry mouth, dizziness/light-headedness, and somnolence/drowsiness. Study limitations include inability to fully exclude data from those <50 years of age in our primary analyses as well as limitations related to weaknesses in the included trials particularly incomplete reporting of outcomes and heterogeneity in included studies.<h4>Conclusions</h4>This pooled analysis, using data from RCTs with mean participant age ≥50 years, suggests that although THC-containing CBMs are associated with side effects, CBMs in general are safe and acceptable in older adults. However, THC:CBD combinations may be less acceptable in the dose ranges used and their tolerability may be different in adults over 65 or 75 years of age.
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