University of Oklahoma Health Sciences College of Pharmacy, Oklahoma City, Oklahoma, USA.
Nova Southeastern University Barry and Judy Silverman College of Pharmacy, Fort Lauderdale, Florida, USA.
Pharmacotherapy. 2024 Nov;44(11):880-891. doi: 10.1002/phar.4622. Epub 2024 Nov 5.
Cannabinoids have emerged as a potential treatment for obstructive sleep apnea (OSA). This systematic review aimed to summarize the efficacy and safety of cannabinoids to treat OSA. Databases including Ovid MEDLINE, EMBASE, Scopus, PsycINFO, and International Pharmaceutical Abstracts were searched; experimental and observational studies were eligible for inclusion. One-hundred seventy unique records were screened, and nine studies included: five full-text studies and four published abstracts. The five full-text studies were judged for quality appraisal: two studies deemed at low risk for bias, one study deemed to have some concerns for bias, and two studies deemed to have high risk for bias. Seven of nine total studies were experimental designs and evaluated dronabinol, and the other two studies were observational designs evaluating cannabis. The range of cannabinoid therapy duration spanned from 1 to 6 weeks, and the median duration was 3 weeks. Eight of nine total studies reported statistically significant, positive OSA outcomes due to cannabinoid therapy including reductions in the apnea hypopnea index and improvements in patient-reported daytime sleepiness scales. Between 70% and 80% of study participants reported neuropsychiatric and gastrointestinal adverse events attributable to cannabinoids. The American Academy of Sleep Medicine does not recommend using cannabinoids to treat OSA due to a lack of long-term safety and efficacy data. This systematic review found similar limitations, with the median cannabinoid treatment duration being only 3 weeks. Adequately powered experimental trials over longer time frames are necessary to more completely assess the long-term efficacy and safety of cannabinoids in the treatment of OSA and its effects on common comorbid conditions, such as obesity and cardiovascular disease.
大麻素类药物已成为治疗阻塞性睡眠呼吸暂停(OSA)的一种潜在方法。本系统评价旨在总结大麻素类药物治疗 OSA 的疗效和安全性。检索了 Ovid MEDLINE、EMBASE、Scopus、PsycINFO 和国际药学文摘数据库;纳入了实验和观察性研究。筛选了 170 条独特的记录,纳入了 9 项研究:5 项全文研究和 4 项已发表的摘要。对 5 项全文研究进行了质量评估:2 项研究认为偏倚风险低,1 项研究认为存在一些偏倚问题,2 项研究认为偏倚风险高。9 项研究中有 7 项为实验设计,评估了大麻隆;另外 2 项研究为观察性设计,评估了大麻。大麻素治疗的持续时间范围从 1 周到 6 周不等,中位数为 3 周。9 项研究中有 8 项报告了由于大麻素治疗而导致的 OSA 结果有统计学意义的阳性结果,包括呼吸暂停低通气指数降低和患者报告的白天嗜睡量表改善。80%至 100%的研究参与者报告了与大麻素相关的神经精神和胃肠道不良事件。由于缺乏长期安全性和疗效数据,美国睡眠医学学会不建议使用大麻素治疗 OSA。本系统评价发现了类似的局限性,大麻素治疗的中位数持续时间仅为 3 周。需要进行更长时间框架的、充分功率的实验试验,以更全面地评估大麻素治疗 OSA 的长期疗效和安全性,及其对肥胖和心血管疾病等常见合并症的影响。