英国基于大麻的医药产品治疗焦虑症患者的临床疗效数据:来自英国医用大麻注册处的队列研究。
Clinical outcome data of anxiety patients treated with cannabis-based medicinal products in the United Kingdom: a cohort study from the UK Medical Cannabis Registry.
机构信息
Imperial College Medical Cannabis Research Group, Department of Surgery and Cancer, Imperial College London, Academic Surgical Unit, 10th Floor QEQM, St Mary's Hospital, South Wharf Road, London, W2 1NY, UK.
Department of Psychological Medicine, King's College London, London, UK.
出版信息
Psychopharmacology (Berl). 2023 Aug;240(8):1735-1745. doi: 10.1007/s00213-023-06399-3. Epub 2023 Jun 14.
RATIONALE
Cannabis-based medicinal products (CBMPs) have been identified as novel therapeutics for generalised anxiety disorder (GAD) based on pre-clinical models; however, there is a paucity of high-quality evidence on their effectiveness and safety.
OBJECTIVES
This study aimed to evaluate the clinical outcomes of patients with GAD treated with dried flower, oil-based preparations, or a combination of both CBMPs.
METHODS
A prospective cohort study of patients with GAD (n = 302) enrolled in the UK Medical Cannabis Registry prescribed oil or flower-based CBMPs was performed. Primary outcomes were changes in generalised anxiety disorder-7 (GAD-7) questionnaires at 1, 3, and 6 months compared to baseline. Secondary outcomes were single-item sleep quality scale (SQS) and health-related quality of life index (EQ-5D-5L) questionnaires at the same time points. These changes were assessed by paired t-tests. Adverse events were assessed in line with CTCAE (Common Terminology Criteria for Adverse Events) v4.0.
RESULTS
Improvements in anxiety, sleep quality and quality of life were observed at each time point (p < 0.001). Patients receiving CBMPs had improvements in GAD-7 at all time points (1 month: difference -5.3 (95% CI -4.6 to -6.1), 3 months: difference -5.5 (95% CI -4.7 to -6.4), 6 months: difference -4.5 (95% CI -3.2 to -5.7)). Thirty-nine participants (12.9%) reported 269 adverse events in the follow-up period.
CONCLUSIONS
Prescription of CBMPs in those with GAD is associated with clinically significant improvements in anxiety with an acceptable safety profile in a real-world setting. Randomised trials are required as a next step to investigate the efficacy of CBMPs.
背景
基于临床前模型,大麻类药物(CBMPs)已被确定为广泛性焦虑症(GAD)的新型治疗药物;然而,关于其有效性和安全性的高质量证据很少。
目的
本研究旨在评估 GAD 患者使用干花、油基制剂或两者联合治疗的临床结果。
方法
对英国医疗大麻登记处登记的 302 例 GAD 患者进行前瞻性队列研究,这些患者被开处油基或花基 CBMPs。主要结局是与基线相比,1、3 和 6 个月时 GAD-7 问卷的变化。次要结局是同时的单项目睡眠质量量表(SQS)和健康相关生活质量指数(EQ-5D-5L)问卷。通过配对 t 检验评估这些变化。根据 CTCAE(不良事件通用术语标准)v4.0 评估不良事件。
结果
在每个时间点都观察到焦虑、睡眠质量和生活质量的改善(p<0.001)。接受 CBMP 治疗的患者在所有时间点的 GAD-7 均有改善(1 个月:差异-5.3(95%置信区间-4.6 至-6.1),3 个月:差异-5.5(95%置信区间-4.7 至-6.4),6 个月:差异-4.5(95%置信区间-3.2 至-5.7))。在随访期间,有 39 名参与者(12.9%)报告了 269 起不良事件。
结论
在现实环境中,处方 CBMPs 治疗 GAD 与焦虑显著改善相关,安全性可接受。下一步需要进行随机试验,以调查 CBMPs 的疗效。