UK Medical Cannabis Registry: a case series analyzing clinical outcomes of medical cannabis therapy for generalized anxiety disorder patients

被引:2
作者
Li, Adam [1 ]
Erridge, Simon [1 ,2 ]
Holvey, Carl [2 ]
Coomber, Ross [2 ,3 ]
Barros, Daniela [2 ]
Bhoskar, Urmila [2 ]
Crews, Matthieu [2 ]
Donnelly, Lorna [2 ]
Imran, Muhammad [2 ]
Korb, Laura [2 ,4 ]
Mwimba, Gracia [2 ]
Sachdeva-Mohan, Simmi [2 ]
Rucker, James J. [5 ,6 ]
Sodergren, Mikael H. [1 ,2 ]
机构
[1] Imperial Coll London, Dept Surg & Canc, Med Cannabis Res Grp, London, England
[2] Sapphire Med Clin, London, England
[3] St Georges Hosp NHS Trust, London, England
[4] North London Mental Hlth Partnership, London, England
[5] Kings Coll London, Dept Psychol Med, London, England
[6] South London & Maudsley NHS Fdn Trust, London, England
关键词
anxiety; cannabidiol; cannabinoids; cannabis; tetrahydrocannabinol; SOCIAL PHOBIA; COMORBIDITY; SYMPTOMS; CB1;
D O I
10.1097/YIC.0000000000000536
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aims to analyze changes in health-related quality of life (HRQoL) and safety in patients with generalized anxiety disorder (GAD) prescribed a homogenous selection of cannabis-based medicinal products (CBMPs). Patients prescribed Adven CBMPs (Curaleaf International, UK) for GAD were identified from the UK Medical Cannabis Registry. Primary outcomes were changes in patient-reported outcome measures (PROMs) from baseline up to 12 months, including GAD-7, Single-Item Sleep Quality Scale (SQS), and EQ-5D-5L. Adverse events were recorded using CTCAE version 4.0. A total of 120 patients were identified for inclusion, of which 38 (31.67%), 52 (43.33%), and 30 (25.00%) were prescribed oils, dried flower, and both formulations of CBMP. Associated improvements in GAD-7, SQS, and EQ-5D-5L at 1, 3, 6, and 12 months were observed compared to baseline (P < 0.010). There were 24 (20.00%) patients who reported 442 (368.33%) adverse events, most of which were mild (n = 184, 41.63%) and moderate (n = 197, 44.57%). This study reports an association between initiation of a homogeneous CBMP therapy and improvements in anxiety severity and HRQoL in individuals with GAD. Moreover, therapy was well-tolerated at 12 months follow-up. Further investigation through randomized controlled trials will ultimately be required to determine causation.
引用
收藏
页码:350 / 360
页数:11
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