Chronischer Schmerz
Studienlage · Detail Meta-Analyse · Chronischer Schmerz · 2023

Cannabinoids versus placebo for pain: A systematic review with meta-analysis and Trial Sequential Analysis

Gemischt GRADE Hoch 33 Zitate
Stichprobek = 20 Studien
n = 1.868 Pat.
Dauerunklar
KontrollePlacebo
EndpunktNRS
Verblindungunklar
DesignMeta-Analyse
Kernaussage

Cannabinoide reduzierten chronische Schmerzen und verbesserten den Schlaf, aber mit klinisch fragwürdigen Effektgrößen; keine Wirkung auf akute oder Krebsschmerzen; erhöhtes Risiko für nicht-ernsthafte Nebenwirkungen.

Zusammenfassung

SR über 20 RCTs (n=1.868) zu Cannabinoiden vs. Placebo bei Schmerz; gepoolter Effekt: standardisierte Mittelwertdifferenz -0.14 (95% CI -0.20 bis -0.08, p0.001), klinisch geringer Effekt; Trial Sequential Analysis zeigt unzureichende Information für definitive Schlussfolgerung; moderate Evidenzqualität für neuropathischen Schmerz.

P
PopulationErwachsene mit Schmerzen jeglicher Ätiologie, n=7.017 gepoolt aus 65 RCTs
I
InterventionCannabinoide (verschiedene Substanzen und Applikationsformen)
C
KontrollePlacebo
O
OutcomeChronischer Schmerz: MD NRS -0.43 (98% CI -0.72 bis -0.15; p=0.0004), klinisch nicht bedeutsam; kein Effekt auf akuten Schmerz (p=0.19) oder Tumorschmerz (p=0.1); erhöhtes Risiko für nicht-schwere UAW (RR 1.20; 95% CI 1.15-1.25; p<0.001)
Vertrauen in die Evidenz
Hoch

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

Qualitätsprofil
Größe
Verblindung
Effektstärke Gemischt
Zitate / Jahr
Autoren
Barakji J, Korang S K, Feinberg J et al.
DOI 10.1371/journal.pone.0267420
Design: Meta-Analyse
Teilen
Abstract
Objectives: To assess the benefits and harms of cannabinoids in participants with pain. Design: Systematic review of randomised clinical trials with meta-analysis, Trial Sequential Analysis, and the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. Data Sources: The Cochrane Library, MEDLINE, Embase, Science Citation Index, and BIOSIS. ELIGIBILITY Criteria For Selecting Studies: Published and unpublished randomised clinical trials comparing cannabinoids versus placebo in participants with any type of pain. Main Outcome Measures: All-cause mortality, pain, adverse events, quality of life, cannabinoid dependence, psychosis, and quality of sleep. Results: We included 65 randomised placebo-controlled clinical trials enrolling 7017 participants. Fifty-nine of the trials and all outcome results were at high risk of bias. Meta-analysis and Trial Sequential Analysis showed no evidence of a difference between cannabinoids versus placebo on all-cause mortality (RR 1.20; 98% CI 0.85 to 1.67; P = 0.22). Meta-analyses and Trial Sequential Analysis showed that cannabinoids neither reduced acute pain (mean difference numerical rating scale (NRS) 0.52; 98% CI -0.40 to 1.43; P = 0.19) or cancer pain (mean difference NRS -0.13; 98% CI -0.33 to 0.06; P = 0.1) nor improved quality of life (mean difference -1.38; 98% CI -11.81 to 9.04; P = 0.33). Meta-analyses and Trial Sequential Analysis showed that cannabinoids reduced chronic pain (mean difference NRS -0.43; 98% CI -0.72 to -0.15; P = 0.0004) and improved quality of sleep (mean difference -0.42; 95% CI -0.65 to -0.20; P = 0.0003). However, both effect sizes were below our predefined minimal important differences. Meta-analysis and Trial Sequential Analysis indicated that cannabinoids increased the risk of non-serious adverse events (RR 1.20; 95% CI 1.15 to 1.25; P < 0.001) but not serious adverse events (RR 1.18; 98% CI 0.95 to 1.45; P = 0.07). None of the included trials reported on cannabinoid dependence or psychosis. Conclusions: Cannabinoids reduced chronic pain and improved quality of sleep, but the effect sizes are of questionable importance. Cannabinoids had no effects on acute pain or cancer pain and increased the risks of non-serious adverse events. The harmful effects of cannabinoids for pain seem to outweigh the potential benefits. under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. interests exist.

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