Department of Anesthesia and Pain Medicine, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Centre for Sleep Health and Research, Toronto General Hospital, Toronto, Ontario, Canada.
J Clin Sleep Med. 2021 Apr 1;17(4):819-824. doi: 10.5664/jcsm.9064.
Approximately 20% of North Americans are afflicted with chronic pain with 3% being opioid users. The objective was to determine whether patients on opioids for chronic pain with newly diagnosed sleep apnea attended sleep clinic review and followed treatment recommendations.
The study was a post hoc analysis from a multicenter perspective cohort study. Inclusion criteria included adults taking opioid medications for chronic pain for >3 months. Demographic data and daily opioid dose were collected. Sleep apnea was diagnosed via level 1 polysomnography. Patients who attended sleep clinic review were grouped based on the types of treatment they received.
A total of 204 patients completed polysomnography and 58.8% were diagnosed to have sleep apnea (apnea-hypopnea index ≥5 events/h). Of those with sleep apnea, 58% were recommended to have an evaluation by a sleep physician. Body mass index and age were 29.5 ± 6 kg/m² and 56 ± 12 years, respectively. Of those with newly diagnosed sleep apnea, 25% received treatment, with the majority being treated with positive airway pressure therapy, whereas the rest received positional therapy and opioids/sedative reduction. The adherence rate of positive airway pressure therapy was 55% at 1 year. Over 50% of participants on opioids for chronic pain with newly diagnosed sleep apnea declined attendance for sleep clinic review or treatment.
There was a high refusal rate to attend clinic for treatment. Adherence to positive airway pressure therapy was low at 55%. This sheds light on the high rate of treatment nonadherence and the need for further research.
Registry: ClinicalTrials.gov; Name: Opioid Safety Program in Pain Clinics (Op-Safe); URL: https://www.clinicaltrials.gov/ct2/show/NCT02513836; Identifier: NCT02513836.
约 20%的北美人患有慢性疼痛,其中 3%是阿片类药物使用者。本研究旨在确定慢性疼痛且新诊断为睡眠呼吸暂停的阿片类药物使用者是否就诊于睡眠诊所并遵循治疗建议。
本研究为一项多中心前瞻性队列研究的事后分析。纳入标准包括服用阿片类药物治疗慢性疼痛超过 3 个月的成年人。收集人口统计学数据和每日阿片类药物剂量。通过 1 级多导睡眠图诊断睡眠呼吸暂停。根据接受的治疗类型,将接受睡眠诊所评估的患者进行分组。
共有 204 例患者完成了多导睡眠图检查,其中 58.8%被诊断为患有睡眠呼吸暂停(呼吸暂停低通气指数≥5 次/小时)。在患有睡眠呼吸暂停的患者中,58%被建议由睡眠医生进行评估。体重指数和年龄分别为 29.5±6kg/m²和 56±12 岁。在新诊断为睡眠呼吸暂停的患者中,25%接受了治疗,其中大多数接受了正压通气治疗,其余患者接受了体位治疗和阿片类药物/镇静剂减少。1 年后,正压通气治疗的依从率为 55%。超过 50%的慢性疼痛且新诊断为睡眠呼吸暂停的阿片类药物使用者拒绝就诊或治疗。
就诊接受治疗的拒绝率很高。正压通气治疗的依从率仅为 55%。这表明治疗不依从率较高,需要进一步研究。
注册机构:ClinicalTrials.gov;名称:疼痛诊所阿片类药物安全计划(Op-Safe);网址:https://www.clinicaltrials.gov/ct2/show/NCT02513836;标识符:NCT02513836。