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Stichproben = 130 Pat.
DesignKohortenstudie
Zusammenfassung
n=130 erwachsene Autist:innen mit CBMP-Verordnung; Verbesserung von GAD-7 (p<0.001) und Schlafqualität SQS (p<0.001) über 18 Monate; EQ-5D-5L-Index 0.43→0.51 (p<0.001); PGIC 5.43→5.65 (p=0.013). Unerwünschte Ereignisse bei 19.23% der Teilnehmenden (232 Ereignisse, überwiegend leicht bis moderat). Ohne Kontrollgruppe nur Assoziationen, keine belegten Behandlungseffekte.
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Abstract
Introduction: Autism spectrum disorder (ASD) is a neurodevelopmental disorder associated with distressed behaviors and psychological challenges. This study aims to evaluate the change in health-related quality of life (HRQoL), anxiety, and sleep quality in autistic individuals prescribed cannabis-based medicinal products (CBMPs).
Method: This observational case series analyzed data from the UK Medical Cannabis Registry on autistic adults treated with CBMPs. Demographic and clinical data were collected at baseline, with patient-reported outcome measures assessed up to 18 months. Primary outcomes included changes in anxiety (GAD-7), sleep quality (SQS), and HRQoL (EQ-5D-5L). Secondary outcomes included the incidence of adverse events. Statistical significance was indicated by p < 0.050.
Results: One-hundred and thirty individuals met the inclusion criteria. GAD-7 (p < 0.001) and SQS (p < 0.001) scores improved from baseline to 18 months. EQ-5D-5L index values showed improvement from baseline (0.43 +/- 0.30) to 18 months (0.51 +/- 0.32, p < 0.001), and PGIC scores increased from 1 month (5.43 +/- 1.49) to 18 months (5.65 +/- 1.32, p = 0.013). Twenty-five participants (19.23%) reported a total of 232 (178.46%) adverse events, with most being mild (n = 88; 67.69%) or moderate (n = 99; 76.15%).
Conclusion: Treatment with CBMPs was associated with improvements in HRQoL, anxiety, and sleep outcomes in autistic patients over an 18-month period. Given the absence of a control group, these findings represent associations rather than proven treatment effects. Further high-quality randomized controlled trials are needed to confirm the long-term efficacy and safety of CBMPs in ASD.
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