PTSD
Study register · detail Meta-Analyse · PTSD · 2019

Cannabinoids for the treatment of mental disorders and symptoms of mental disorders: a systematic review and meta-analysis

No benefit demonstrated GRADE High 557 citations
Samplek = 83 Studien
n = 3.067 Pat.
DurationStudies published between Jan…
ControlPlacebo
EndpointSymptom change in mental…
Blindingdoppelblind
DesignMeta-Analyse
Key finding

Cannabinoids show hardly any evidence for improving depression, anxiety disorders, ADHD, Tourette syndrome, PTSD or psychosis; only very weak evidence for small improvement of anxiety symptoms in other conditions, but increased side effects.

Summary

Comprehensive SR + meta-analysis of medical cannabinoids (cannabis, pharmaceutical cannabinoids, THC, CBD) in mental disorders (depression, anxiety, ADHD, Tourette, PTSD, psychosis); databases 1980–2018. Primary outcomes: remission and symptom change. Evidence synthesis via random-effects meta-analyses (OR for remission/adverse events, SMD for symptom change). GRADE quality assessment. Included for PTSD as one of the indications examined.

P
PopulationAdults (≥18 years) with mental disorders (depression, anxiety, ADHD, Tourette syndrome, PTSD, psychosis), pooled n=3067 from RCTs
I
InterventionMedical cannabinoids (pharmaceutical THC ± CBD, CBD alone, medical cannabis, synthetic derivatives)
C
ControlPlacebo
O
OutcomePharmaceutical THC (± CBD) slightly improved anxiety symptoms in comorbid conditions (SMD −0,25 [95% CI −0,49 to −0,01]; very low quality evidence); worsened negative psychosis symptoms in one study (SMD 0,36 [95% CI 0,10–0,62]); increased adverse events (OR 1,99 [95% CI 1,20–3,29]) and discontinuation rates (OR 2,78 [95% CI 1,59–4,86]) versus placebo
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 No benefit
Citations / year
Authors
Black N, Stockings E, Campbell G et al.
DOI 10.1016/s2215-0366(19)30401-8
Design: Meta-Analyse
Share
Abstract
Background: Medicinal cannabinoids, including medicinal cannabis and pharmaceutical cannabinoids and their synthetic derivatives, such as tetrahydrocannabinol (THC) and cannabidiol (CBD), have been suggested to have a therapeutic role in certain mental disorders. We analysed the available evidence to ascertain the effectiveness and safety of all types of medicinal cannabinoids in treating symptoms of various mental disorders. Methods: For this systematic review and meta-analysis we searched MEDLINE, Embase, PsycINFO, the Cochrane Central Register of Controlled Clinical Trials, and the Cochrane Database of Systematic Reviews for studies published between Jan 1, 1980, and April 30, 2018. We also searched for unpublished or ongoing studies on ClinicalTrials.gov, the EU Clinical Trials Register, and the Australian and New Zealand Clinical Trials Registry. We considered all studies examining any type and formulation of a medicinal cannabinoid in adults (>/=18 years) for treating depression, anxiety, attention-deficit hyperactivity disorder (ADHD), Tourette syndrome, post-traumatic stress disorder, or psychosis, either as the primary condition or secondary to other medical conditions. We placed no restrictions on language, publication status, or study type (ie, both experimental and observational study designs were included). Primary outcomes were remission from and changes in symptoms of these mental disorders. The safety of medicinal cannabinoids for these mental disorders was also examined. Evidence from randomised controlled trials was synthesised as odds ratios (ORs) for disorder remission, adverse events, and withdrawals and as standardised mean differences (SMDs) for change in symptoms, via random-effects meta-analyses. The quality of the evidence was assessed with the Cochrane risk of bias tool and Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach. This study is registered with PROSPERO (CRD42017059372, CRD42017059373, CRD42017059376, CRD42017064996, and CRD42018102977). Findings: 83 eligible studies (40 randomised controlled trials, n=3067) were included: 42 for depression (23 randomised controlled trials; n=2551), 31 for anxiety (17 randomised controlled trials; n=605), eight for Tourette syndrome (two randomised controlled trials; n=36), three for ADHD (one randomised controlled trial; n=30), 12 for post-traumatic stress disorder (one randomised controlled trial; n=10), and 11 for psychosis (six randomised controlled trials; n=281). Pharmaceutical THC (with or without CBD) improved anxiety symptoms among individuals with other medical conditions (primarily chronic non-cancer pain and multiple sclerosis; SMD -0.25 [95% CI -0.49 to -0.01]; seven studies; n=252), although the evidence GRADE was very low. Pharmaceutical THC (with or without CBD) worsened negative symptoms of psychosis in a single study (SMD 0.36 [95% CI 0.10 to 0.62]; n=24). Pharmaceutical THC (with or without CBD) did not significantly affect any other primary outcomes for the mental disorders examined but did increase the number of people who had adverse events (OR 1.99 [95% CI 1.20 to 3.29]; ten studies; n=1495) and withdrawals due to adverse events (2.78 [1.59 to 4.86]; 11 studies; n=1621) compared with placebo across all mental disorders examined. Few randomised controlled trials examined the role of pharmaceutical CBD or medicinal cannabis. Interpretation: There is scarce evidence to suggest that cannabinoids improve depressive disorders and symptoms, anxiety disorders, attention-deficit hyperactivity disorder, Tourette syndrome, post-traumatic stress disorder, or psychosis. There is very low quality evidence that pharmaceutical THC (with or without CBD) leads to a small improvement in symptoms of anxiety among individuals with other medical conditions. There remains insufficient evidence to provide guidance on the use of cannabinoids for treating mental disorders within a regulatory framework. Further high-quality studies directly examining the effect of cannabinoids on treating mental disorders are needed. Funding: Therapeutic Goods Administration, Australia; Commonwealth Department of Health, Australia; Australian National Health and Medical Research Council; and US National Institutes of Health.

The impediment to action advances action. — Marcus Aurelius