Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada
Division of Respirology, Department of Medicine, St Michael's Hospital, Toronto, Ontario, Canada.
Thorax. 2021 Jan;76(1):29-36. doi: 10.1136/thoraxjnl-2020-215346. Epub 2020 Sep 30.
Respiratory-related morbidity and mortality were evaluated in relation to incident prescription oral synthetic cannabinoid (nabilone, dronabinol) use among older adults with chronic obstructive pulmonary disease (COPD).
This was a retrospective, population-based, data-linkage cohort study, analysing health administrative data from Ontario, Canada, from 2006 to 2016. We identified individuals aged 66 years and older with COPD, using a highly specific, validated algorithm, excluding individuals with malignancy and those receiving palliative care (n=185 876 after exclusions). An equivalent number (2106 in each group) of new cannabinoid users (defined as individuals dispensed either nabilone or dronabinol, with no dispensing for either drug in the year previous) and controls (defined as new users of a non-cannabinoid drug) were matched on 36 relevant covariates, using propensity scoring methods. Cox proportional hazard regression was used.
Rate of hospitalisation for COPD or pneumonia was not significantly different between new cannabinoid users and controls (HR 0.87; 95% CI 0.61-1.24). However, significantly higher rates of all-cause mortality occurred among new cannabinoid users compared with controls (HR 1.64; 95% CI 1.14-2.39). Individuals receiving higher-dose cannabinoids relative to controls were observed to experience both increased rates of hospitalisation for COPD and pneumonia (HR 2.78; 95% CI 1.17-7.09) and all-cause mortality (HR 3.31; 95% CI 1.30-9.51).
New cannabinoid use was associated with elevated rates of adverse outcomes among older adults with COPD. Although further research is needed to confirm these observations, our findings should be considered in decisions to use cannabinoids among older adults with COPD.
评估了与慢性阻塞性肺疾病(COPD)老年患者中出现的处方口服合成大麻素(纳比隆、屈大麻酚)使用相关的呼吸系统相关发病率和死亡率。
这是一项回顾性、基于人群的、数据链接队列研究,分析了来自加拿大安大略省的健康管理数据,时间范围为 2006 年至 2016 年。我们使用高度特异性、经过验证的算法确定了年龄在 66 岁及以上的 COPD 患者,排除了患有恶性肿瘤和接受姑息治疗的患者(排除后共有 185876 人)。使用倾向评分方法,根据 36 个相关协变量,为每个组的 2106 名新大麻素使用者(定义为配给纳比隆或屈大麻酚的个体,在之前的一年中两种药物都没有配给)和对照组(定义为新使用非大麻素药物的个体)进行了匹配。使用 Cox 比例风险回归进行分析。
新大麻素使用者与对照组之间 COPD 或肺炎住院的发生率没有显著差异(HR 0.87;95%CI 0.61-1.24)。然而,与对照组相比,新大麻素使用者的全因死亡率明显更高(HR 1.64;95%CI 1.14-2.39)。与对照组相比,接受更高剂量大麻素的个体,无论是 COPD 还是肺炎的住院率都有所增加(HR 2.78;95%CI 1.17-7.09),全因死亡率也有所增加(HR 3.31;95%CI 1.30-9.51)。
新大麻素的使用与 COPD 老年患者不良结局的发生率升高有关。尽管需要进一步的研究来证实这些观察结果,但我们的发现应该在决定是否在 COPD 老年患者中使用大麻素时加以考虑。