Angststörungen
Studienlage · Detail Meta-Analyse · Angststörungen · 2015

Cannabinoids for Medical Use

Gemischt GRADE Hoch 2103 Zitate
Stichprobek = 79 Studien
n = 6.462 Pat.
Dauerunklar
KontrollePlacebo
EndpunktSchmerzintensität
Verblindungunklar
DesignMeta-Analyse
Kernaussage

Moderate Evidenz für chronische Schmerzen und Spastizität, niedrige Evidenz für Übelkeit/Erbrechen, Gewichtszunahme und Schlafstörungen; erhöhtes Risiko für Nebenwirkungen.

Zusammenfassung

Umfassende SR über 79 RCTs (n=6.462) zu medizinischem Cannabis; KEINE ausreichende Evidenz für Angststörungen als primäres Outcome — moderate Evidenz nur für Schmerz und MS-Spastik, Angst nur als sekundäres/exploratives Outcome in einigen Studien.

P
PopulationErwachsene mit verschiedenen Indikationen (chronischer Schmerz, MS-Spastik, Chemotherapie-induzierte Übelkeit/Erbrechen, HIV/AIDS-Appetitlosigkeit, Schlafstörungen, Tourette-Syndrom u.a.), n=6.462 aus 79 RCTs
I
InterventionCannabinoide (verschiedene Substanzen und Applikationsformen)
C
KontrollePlacebo
O
OutcomeModerate Evidenz für chronischen Schmerz (OR 1,41 [95% CI 0,99-2,00], WMD -0,46 auf 0-10-Skala) und Spastik (WMD -0,36 Ashworth-Skala); niedrige Evidenz für Übelkeit/Erbrechen (OR 3,82 [95% CI 1,55-9,42]), Gewichtszunahme bei HIV, Schlafstörungen und Tourette-Syndrom. Erhöhtes Risiko für kurzfristige unerwünschte Ereignisse (Schwindel, Mundtrockenheit, Fatigue, Somnolenz, Euphorie, Desorientiertheit)
Vertrauen in die Evidenz
Hoch

Höchste von vier GRADE-Stufen, die Effektschätzung ist sehr verlässlich.

Qualitätsprofil
Größe
Verblindung
Effektstärke Gemischt
Zitate / Jahr
Autoren
Whiting P F, Wolff R F, Deshpande S et al.
DOI 10.1001/jama.2015.6358
Design: Meta-Analyse
Teilen
Abstract
Importance: Cannabis and cannabinoid drugs are widely used to treat disease or alleviate symptoms, but their efficacy for specific indications is not clear. Objective: To conduct a systematic review of the benefits and adverse events (AEs) of cannabinoids. Data Sources: Twenty-eight databases from inception to April 2015. Study Selection: Randomized clinical trials of cannabinoids for the following indications: nausea and vomiting due to chemotherapy, appetite stimulation in HIV/AIDS, chronic pain, spasticity due to multiple sclerosis or paraplegia, depression, anxiety disorder, sleep disorder, psychosis, glaucoma, or Tourette syndrome. Data Extraction And Synthesis: Study quality was assessed using the Cochrane risk of bias tool. All review stages were conducted independently by 2 reviewers. Where possible, data were pooled using random-effects meta-analysis. Main Outcomes And Measures: Patient-relevant/disease-specific outcomes, activities of daily living, quality of life, global impression of change, and AEs. Results: A total of 79 trials (6462 participants) were included; 4 were judged at low risk of bias. Most trials showed improvement in symptoms associated with cannabinoids but these associations did not reach statistical significance in all trials. Compared with placebo, cannabinoids were associated with a greater average number of patients showing a complete nausea and vomiting response (47% vs 20%; odds ratio [OR], 3.82 [95% CI, 1.55-9.42]; 3 trials), reduction in pain (37% vs 31%; OR, 1.41 [95% CI, 0.99-2.00]; 8 trials), a greater average reduction in numerical rating scale pain assessment (on a 0-10-point scale; weighted mean difference [WMD], -0.46 [95% CI, -0.80 to -0.11]; 6 trials), and average reduction in the Ashworth spasticity scale (WMD, -0.36 [95% CI, -0.69 to -0.05]; 7 trials). There was an increased risk of short-term AEs with cannabinoids, including serious AEs. Common AEs included dizziness, dry mouth, nausea, fatigue, somnolence, euphoria, vomiting, disorientation, drowsiness, confusion, loss of balance, and hallucination. Conclusions And Relevance: There was moderate-quality evidence to support the use of cannabinoids for the treatment of chronic pain and spasticity. There was low-quality evidence suggesting that cannabinoids were associated with improvements in nausea and vomiting due to chemotherapy, weight gain in HIV infection, sleep disorders, and Tourette syndrome. Cannabinoids were associated with an increased risk of short-term AEs.

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