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UK registry study found early PTSD score improvements, then a plateau

Cannabis-based medicinal products for post-traumatic stress disorder: a two-year prospective analysis from the UK medical cannabis registry.

Psychopharmacology β€’ β€’ Highly Relevant
πŸ€–

AI Summary

This prospective, uncontrolled case series asked whether patient-reported symptoms changed among 446 UK registry patients with PTSD prescribed cannabis-based medicinal products (CBMPs), with follow-up for up to 24 months. Mean PTSD symptom, anxiety, sleep-quality, and health-related quality-of-life scores improved from baseline at all reported follow-up times. The average PTSD symptom score improved most during the first month and then plateaued; at 24 months, 55.38% of patients still met the stated DSM-IV threshold for PTSD. Many patients were already using cannabis before treatment began.

At least one adverse event was reported by 16.82% of patients; among the recorded events, 14.36% were severe and 0.35% were life-threatening or disabling. These results describe changes observed during treatment, not proof that CBMPs caused them. The study had no control group, substantial attrition, and extensive imputation of 24-month PTSD scores; the authors therefore state that it cannot establish efficacy or causality.

πŸ’‘ Key Findings

1
Mean PTSD symptom, anxiety, sleep-quality, and health-related quality-of-life scores improved from baseline at reported follow-ups; improvement was concentrated in the first month and then plateaued.
High
90%
2
At 24 months, 55.38% of patients still met the stated DSM-IV threshold for PTSD.
High
90%
3
16.82% of patients reported at least one adverse event; 14.36% of recorded events were severe, and 0.35% were life-threatening or disabling.
High
90%
4
This uncontrolled case series, with high attrition and substantial imputation of 24-month PTSD scores, cannot establish that CBMPs caused the observed changes or were effective.
High
100%

πŸ“„ Original Abstract

RATIONALE: Post-traumatic stress disorder (PTSD) is characterised by persistent psychological symptoms following exposure to trauma. Cannabis-based medicinal products (CBMPs) have promising therapeutic potential. However, there is a paucity of long-term studies investigating their use. OBJECTIVES: This prospective case series aimed to assess changes in patient-reported outcome measures (PROMs) and the prevalence of adverse events in patients prescribed CBMPs for PTSD. METHODS: Patients enrolled on the United Kingdom Medical Cannabis Registry for PTSD were included. Changes in PROMs (Impact of Events Scale-Revised (IES-R), Generalised Anxiety Disorder-7 (GAD-7), Single-Item Sleep Quality Scale (SQS) and EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5​L)) were assessed from baseline up to 24 months. RESULTS: In total, 446 patients were included, of which 75.11% (n = 335) were already using cannabis before starting treatment. Mean IES-R, GAD-7, SQS and EQ-5D-5​L scores improved relative to baseline at all follow-up times (p < 0.001). At 24 months, 64.57% (n = 288) of IES-R data were imputed. The mean IES-R fell from 59.58 ± 15.93 at baseline to 36.91 ± 18.56 at 24 months, with 55.38% (n = 247) of patients continuing to meet the DSM-IV threshold for PTSD at 24 months. Seventy-five patients (16.82%) reported at least one adverse event. Of 578 events, 83 (14.36%) were severe, and 2 (0.35%) life-threatening or disabling. CONCLUSION: In this uncontrolled case series, CBMP treatment was associated with improvements in mean PTSD symptom, anxiety, sleep, and health-related quality of life scores. However, the improvement was concentrated within the first month and then plateaued. The observational design, high attrition, and reliance on imputed data preclude any inference of efficacy or causality.

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