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3 Zitate
Stichproben = 148 Pat.
Dauer12 Monate
EndpunktGAD-7, Schlafqualität…
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DesignKohortenstudie
Cannabinoidvollspektrum
Kernaussage
Verbesserungen bei Angststörungen, Schlafqualität, Fibromyalgie-Symptomstärke und Lebensqualität (EQ-5D-5L) über alle Follow-up-Perioden im Vergleich zur Baseline (p < 0,050).
Zusammenfassung
n=148 Fibromyalgie-Patienten aus UK Medical Cannabis Registry, behandelt mit Cannabis-Ölen (52%), Blüten (9,5%) oder Kombination (38,5%). Verbesserungen bei GAD-7, Schlafqualität, Fibromyalgie-Symptomschwere und EQ-5D-5L Index bei allen Follow-ups vs. Baseline (p<0,050). 36 Patienten (24,3%) berichteten 648 Nebenwirkungen, häufiger bei Cannabis-naiven Patienten. Keine Unterschiede zwischen CBMP-Formulierungen.
P
PopulationFibromyalgie-Patienten aus dem UK Medical Cannabis Registry, n=148
I
InterventionCannabis-basierte Medizinprodukte (Öle und/oder Blüten, Adven, Curaleaf International, UK), oral oder inhalativ
O
OutcomeSignifikante Verbesserungen in GAD-7, Schlafqualität, Fibromyalgie-Symptomschwerescore und EQ-5D-5L-Indexwerten zu allen Follow-up-Zeitpunkten vs. Baseline (p<0.050); 24,32% der Patienten berichteten über 648 unerwünschte Ereignisse
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Abstract
This cohort study aims to assess the outcomes of fibromyalgia patients enrolled in the UK Medical Cannabis Registry prescribed a homogenous selection of cannabis-based medicinal products (CBMPs). A cohort study of fibromyalgia patients treated with oils (Adven((R)), Curaleaf International, UK), dried flower (Adven((R)), Curaleaf International, UK) or both CBMPs was performed. Primary outcomes were changes from baseline at 1, 3, 6 and 12 months in validated patient-reported outcome measures. Secondary outcomes included descriptive analysis of adverse events. One hundred and forty-eight participants were treated with oils (n = 77; 52.03%), dried flower (n = 14; 9.46%) or both (n = 57; 38.51%). Improvements in the generalized anxiety disorder-7 questionnaire, single-item sleep quality scale, fibromyalgia symptom severity score and EQ-5D-5L Index values were observed at each follow up period compared to baseline (p < 0.050). Thirty-six (24.32%) patients experienced 648 adverse events. Improvements were observed across all primary outcomes with no differences observed across different formulations of CBMPs. Adverse events were reported by one-quarter of participants and were more likely to reported by cannabis naive patients. This present work through focusing on a homogeneous group of CBMPs can help inform randomized controlled trials after observing signals of improvement associated with a specific cultivar of CBMPs.
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