UK Medical Cannabis Registry: An Analysis of Clinical Outcomes of Medicinal Cannabis Therapy for Cancer Pain.

IF 0.9 Q3 ANESTHESIOLOGY
Madhur Varadpande, Simon Erridge, Arushika Aggarwal, Isaac Cowley, Lilia Evans, Evonne Clarke, Katy McLachlan, Ross Coomber, James J Rucker, Michael W Platt, Shaheen Khan, Mikael Sodergren
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Abstract

Cancer pain (CP) is a prevalent condition with limited pharmacotherapeutic options. Cannabis-based medicinal products (CBMPs) have shown analgesic effects, but their efficacy in CP remains contentious. This study aims to evaluate the change in patient-reported outcome measures (PROMs) and adverse events (AEs) in CP patients treated with CBMPs. A case series was conducted using prospectively collected clinical data from the UK Medical Cannabis Registry. Primary outcomes were the changes in the Brief Pain Inventory (BPI), pain visual analogue scale (Pain-VAS), EQ-5D-5L, Generalized Anxiety Disorder-7 (GAD-7), Patient Global Impression of Change (PGIC) and Single-Item Sleep Quality Scale (SQS) questionnaires from baseline to 1, 3, and 6 months. AEs were recorded and graded. p < 0.050 was considered statistically significant. One hundred and sixty-eight participants were included. CBMPs were associated with improvements in all pain-specific PROMs at all follow-up periods (p < 0.050). Improvements in GAD-7, SQS, and EQ-5D-5L index scores were also observed (p < 0.050). Twenty-nine AEs (17.26%) were reported by five patients (2.98%), mostly mild-to-moderate (72.41%). Although the observational design means causality cannot be established, the findings support the development of future randomized controlled trials into CP management with CBMPs.

英国医用大麻登记处:药用大麻治疗癌症疼痛的临床结果分析。
癌性疼痛(CP)是一种普遍的疾病,药物治疗选择有限。以大麻为基础的药物(CBMPs)已显示出镇痛作用,但其对CP的疗效仍有争议。本研究旨在评估接受CBMPs治疗的CP患者报告的预后指标(PROMs)和不良事件(ae)的变化。使用从联合王国医用大麻登记处前瞻性收集的临床数据进行了病例系列研究。主要结果是从基线到1、3和6个月的简短疼痛量表(BPI)、疼痛视觉模拟量表(Pain- vas)、EQ-5D-5L、广泛性焦虑障碍-7 (GAD-7)、患者整体变化印象(PGIC)和单项睡眠质量量表(SQS)问卷的变化。记录ae并评分。P < 0.050认为有统计学意义。共纳入168名参与者。在所有随访期间,CBMPs与所有疼痛特异性prom的改善相关(p < 0.050)。GAD-7、SQS和EQ-5D-5L指标评分也有改善(p < 0.050)。5例患者(2.98%)报告29例不良事件(17.26%),多为轻中度不良事件(72.41%)。虽然观察性设计意味着因果关系无法确定,但研究结果支持未来随机对照试验的发展,以cbmp治疗CP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.60
自引率
9.10%
发文量
40
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