PTBS
Studienlage · Detail Kohortenstudie · PTBS · 2025

UK medical cannabis registry: an updated clinical outcomes analysis of patients with post-traumatic stress disorder.

Klarer Nutzen GRADE Niedrig 3 Zitate
Stichproben = 269 Pat.
Dauer18 Monate
EndpunktIES-R
Verblindungn.a.
DesignKohortenstudie
Kernaussage

Signifikante Verbesserungen in PTSD-Symptomen, Angst, Schlafqualität und allgemeiner Lebensqualität bei allen Nachbeobachtungspunkten bis 18 Monate (p < 0,001).

Zusammenfassung

UK Medical Cannabis Registry, n=269 PTSD-Patienten über 18 Monate. Signifikante Verbesserungen in IES-R (PTSD-Symptome), GAD-7 (Angst), SQS (Schlafqualität) und EQ-5D-5L (Lebensqualität) zu allen Follow-up-Zeitpunkten (p<0.001). Männliches Geschlecht assoziiert mit reduzierter Chance auf IES-R-Verbesserung (OR=0.51, 95% CI 0.28–0.94, p=0.034). Nebenwirkungen bei 70 Patienten (26.02%), häufigste: Insomnie (15.61%), Fatigue (14.87%).

P
PopulationPTSD-Patienten, die im UK Medical Cannabis Registry eingeschlossen waren (≥18 Monate), n=269
I
InterventionCannabis-basierte Medizinprodukte (CBMPs), verschreibungspflichtig, Langzeitanwendung
O
OutcomeSignifikante Verbesserungen in PTSD-Symptomen (IES-R), Angst (GAD-7), Schlafqualität (SQS) und HRQoL (EQ-5D-5L) zu allen Follow-up-Zeitpunkten (p<0,001); männliches Geschlecht assoziiert mit geringerer Wahrscheinlichkeit einer IES-R-Verbesserung (OR=0,51; 95%-KI: 0,28–0,94; p=0,034)
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Niedrig

Zweite von vier GRADE-Stufen, die Effektschätzung ist begrenzt verlässlich.

Qualitätsprofil
Größe
Verblindung
Effektstärke Klarer Nutzen
Zitate / Jahr
Autoren
Datta A, Erridge S, Warner-Levy J, Clarke E, McLachlan K, Coomber R, Asghar M, Bhoskar U, Crews M, De Angelis A
DOI 10.1080/14737175.2025.2490539
Design: Kohortenstudie
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Abstract
Background: Cannabis-based medicinal products (CBMPs) are a potential treatment for post-traumatic stress disorder (PTSD), but their long-term efficacy and safety need further investigation. This study assessed the changes in health-related quality of life (HRQoL) and adverse events in PTSD patients prescribed CBMPs. Research Design And Methods: This observational cohort study included PTSD patients enrolled on the UK Medical Cannabis Registry for 18 months or longer. Changes in PTSD-specific symptoms (IES-R), anxiety (GAD-7), sleep quality (SQS), and general HRQoL (EQ-5D-5 L) were assessed at 1, 3, 6, 12, and 18 months. Results: In 269 patients, significant improvements in PTSD symptoms, anxiety, sleep quality, and HRQoL were observed at all follow-up points (p < 0.001). On multivariate logistic regression, male gender (OR = 0.51; 95% CI:0.28-0.94; p = 0.034) was associated with a reduced chance of reporting improvements in IES-R. Adverse events were reported by 70 (26.02%) patients, with insomnia (n = 42, 15.61%) and fatigue (n = 40, 14.87%) being the most common. Conclusions: CBMPs were associated with improvements in PTSD symptoms, anxiety, sleep, and HRQoL at up to 18 months. Although the study's observational nature limits causal conclusions, these findings support further assessment of medical cannabis. Trial Registration: This is an observational study and is not registered as a clinical trial.

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