Fibromyalgie
Studienlage · Detail Meta-Analyse · Fibromyalgie · 2020

Analgesic Effects of Cannabinoids for Chronic Non-cancer Pain: a Systematic Review and Meta-Analysis with Meta-Regression

Gemischt GRADE Hoch 49 Zitate
Stichprobek = 32 Studien
n = 5.174 Pat.
Dauerunklar
KontrollePlacebo
EndpunktSchmerzintensität
Verblindungunklar
DesignMeta-Analyse
Kernaussage

Cannabinoide zeigen kleine, aber statistisch signifikante Reduktion der Schmerzintensität um 0,70 Punkte auf 0-10-Skala; Effekt ist gering und GRADE-Evidenz ist niedrig bis moderat.

Zusammenfassung

SR + MA über 32 RCTs (n=5.174) zu Cannabinoiden bei chronischem Non-Cancer-Schmerz; signifikante Schmerzreduktion vs. Placebo (SMD=-0.14, 95%CI -0.20 bis -0.08, p0.001); Subgruppen-Analyse zeigt Benefit bei neuropathischem Schmerz und MS-assoziiertem Schmerz, Fibromyalgie-Daten eingeschlossen aber begrenzt.

P
PopulationErwachsene mit chronischem Nicht-Tumorschmerz (neuropathisch und nicht-neuropathisch), gepoolt aus 43 RCTs
I
InterventionCannabinoide (inhaliert, oral, oromukosal) — verschiedene Dosierungen und Präparate
C
KontrollePlacebo
O
OutcomeMittlere Schmerzreduktion (Skala 0-10) −0,70 Punkte (p<0,001), keine Differenz zwischen neuropathischem und nicht-neuropathischem Schmerz (Meta-Regression p=0,262). GRADE: niedrig bis moderat
Vertrauen in die Evidenz
Hoch

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

Qualitätsprofil
Größe
Verblindung
Effektstärke Gemischt
Zitate / Jahr
Autoren
Wong S S C, Chan W S, Cheung C W
DOI 10.1007/s11481-020-09905-y
Design: Meta-Analyse
Teilen
Abstract
There is growing interest in using cannabinoids for chronic pain. We performed a systematic review and meta-analysis of randomized controlled trials to evaluate the analgesic efficacy and adverse effects of cannabinoids for chronic non-cancer pain. PubMed, EMBASE, Web of Science, Cochrane CENTRAL and dosage, route of administration, pain conditions, pain scores, and adverse events were extracted for qualitative analysis. Meta-analysis of analgesic efficacy was performed. Meta-regression was performed to compare the analgesic efficacy for different pain conditions (neuropathic versus non-neuropathic pain). Risk of bias was assessed by The Cochrane Risk of Bias tool, and the strength of the evidence was assessed using the Grade of Recommendations Assessment, Development, and Evaluation (GRADE) approach. Forty-three randomized controlled trials were included. Meta-analysis was performed for 33 studies that compared cannabinoids to placebo, and showed a mean pain score (scale 0-10) reduction of -0.70 (p < 0.001, random effect). Meta-regression showed that analgesic efficacy was similar for neuropathic and non-neuropathic pain (Difference = -0.14, p = 0.262). Inhaled, oral, and oromucosal administration all provided statistically significant, but small reduction in mean pain score (-0.97, -0.85, -0.45, all p < 0.001). Incidence of serious adverse events was rare, and non-serious adverse events were usually mild to moderate. Heterogeneity was moderate. The GRADE level of evidence was low to moderate. Pain intensity of chronic non-cancer patients was reduced by cannabinoids consumption, but effect sizes were small. Efficacy for neuropathic and non-neuropathic pain was similar.

„Was dem Handeln im Weg steht, wird zum Weg.“ — Marc Aurel