Ghosh Aishwarya, Erridge Simon, Coomber Ross, Bhoskar Urmila, Holden Wendy, Kamal Fariha, Mwimba Gracia, Sachdeva-Mohan Simmi, Shaya Gabriel, Usmani Azfer, Rucker James, Sodergren Mikael
Eur Addict Res. 2025 Jul 30:1-18. doi: 10.1159/000547696.
With a global rise in opioid-related mortality, comes a need to address this with novel therapies. Cannabinoid receptors are highly expressed and co-localised with opiate receptors of the mesolimbic system. Cannabis-based medicinal products (CBMPs) have been suggested as a measure to reduce harm as maintenance therapy for substance use disorder (SUD).
To assess changes in patient-reported outcomes measures (PROMs) and opioid medications in individuals treated with CBMPs for SUD.
Data from patients with SUD from the UK Medical Cannabis Registry was analysed. Outcomes included changes at 1, 3, and 6 months from baseline of the EQ-5D-DL, single-item sleep quality scale (SQS) and Generalised Anxiety Disorder-7 (GAD-7) questionnaire. Change in opioid medications was assessed as change in oral morphine equivalent (OME).
Thirty-four patients were included. Twenty-seven (79.41%) participants were male. Twenty-nine (85.29%) participants were illicit cannabis consumers at baseline. The most common SUD was opioid use disorder (n=18; 52.94%). Four (11.76%), 14 (41.18%), and 16 (47.05%), patients were prescribed oils, dried flower or a combination of dried flower and oils, respectively. Improvements in GAD-7, SQS, and EQ-5D-5L at 1, 3, and 6 months from baseline were observed (p<0.050). Median OME consumption at baseline was 274.95 [79.50-441.80] mg/day. This was reduced at 6 months (204.45 [61.88-354.85] mg/day; p=0.043), there was no significant difference at 1 or 3 months (p>0.050). Three (8.81%) participants reported 17 (50.00%) adverse events.
There was an associated improvement in health-related quality of life PROMs and reduction in prescribed opioids in individuals with SUD treated with CBMPs. CBMPs were well tolerated by most individuals in this 6-month analysis. Further evaluation through randomised controlled trials is needed to determine causality. .
随着全球阿片类药物相关死亡率的上升,需要采用新的疗法来应对这一问题。大麻素受体在中脑边缘系统中高度表达且与阿片受体共定位。基于大麻的药用产品(CBMPs)已被提议作为减少危害的一种措施,用于物质使用障碍(SUD)的维持治疗。
评估接受CBMPs治疗的SUD患者报告结局指标(PROMs)和阿片类药物的变化。
分析了来自英国医用大麻登记处的SUD患者数据。结局指标包括从基线起1个月、3个月和6个月时EQ-5D-DL、单项睡眠质量量表(SQS)和广泛性焦虑障碍-7(GAD-7)问卷的变化。阿片类药物的变化以口服吗啡当量(OME)的变化来评估。
纳入了34名患者。27名(79.41%)参与者为男性。29名(85.29%)参与者在基线时为非法大麻使用者。最常见的SUD是阿片类药物使用障碍(n = 18;52.94%)。分别有4名(11.76%)、14名(41.18%)和16名(47.05%)患者被开具了油剂、干花或干花与油剂的组合。观察到从基线起1个月、3个月和6个月时GAD-7、SQS和EQ-5D-5L有所改善(p < 0.050)。基线时OME的中位消耗量为274.95 [79.50 - 441.80]毫克/天。在6个月时有所减少(204.45 [61.88 - 354.85]毫克/天;p = 0.043),在1个月或3个月时无显著差异(p > 0.050)。3名(8.81%)参与者报告了17起(50.00%)不良事件。
接受CBMPs治疗的SUD患者的健康相关生活质量PROMs有所改善,且开具的阿片类药物减少。在这项为期6个月的分析中,大多数个体对CBMPs耐受性良好。需要通过随机对照试验进行进一步评估以确定因果关系。