DeVido Jeffrey, Connery Hilary, Hill Kevin P
Division of Alcohol and Drug Abuse, McLean Hospital, Belmont, Massachusetts; Department of Psychiatry, University of California, San Francisco, San Francisco, California.
Division of Alcohol and Drug Abuse, McLean Hospital, Belmont, Massachusetts; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts.
J Opioid Manag. 2015 Jul-Aug;11(4):363-6. doi: 10.5055/jom.2015.0285.
Rates of opioid overdose deaths are increasing in the United States, leading to intensified efforts to provide medication-assisted treatments for opioid use disorders. It is not clear what effect opioid agonist treatments (ie, the µ-opioid receptor full agonist methadone and the partial agonist buprenorphine) may have on respiratory function. However, sleep-disordered breathing has been documented in methadone maintenance pharmacotherapy, and there is emerging evidence for similar sleep-disordered breathing in buprenorphine and buprenorphine-naloxone maintenance treatment.
To provide further clinical evidence of sleep-disordered breathing emerging in the context of buprenorphine-naloxone maintenance pharmacotherapy.
The authors report two additional cases of sleep-disordered breathing that developed in patients with severe opioid use disorders, treated successfully as outpatients with buprenorphine-naloxone maintenance. Both patients provided written consent for their clinical information to be included in this case report, and elements of their identities have been masked to provide confidentiality.
Two adult female patients, who were stable in buprenorphine-naloxone maintenance treatment developed daytime sleepiness, were referred for evaluation and found to have sleep-disordered breathing. One patient's daytime sleepiness improved with reduction in both buprenorphine-naloxone and other sedating medications as well as initiation of a constant positive airway pressure (CPAP) device. However, the other patient could not tolerate decreases in buprenorphine-naloxone and/or CPAP initiation and her daytime sleepiness persisted.
Buprenorphine-naloxone maintenance treatment can be associated with sleep-disordered breathing. It can be difficult to differentiate the cause(s) of sleep-disordered breathing among the effects of buprenorphine-naloxone treatment itself, co-occurring conditions, such as obesity and cigarette smoking or other medications, or some combination thereof. Regardless of etiology, sleep-disordered breathing and its consequences present unique challenges to the patient in recovery from an opioid use disorder and therefore warrants careful evaluation and management.
美国阿片类药物过量致死率不断上升,促使人们加大力度为阿片类药物使用障碍提供药物辅助治疗。目前尚不清楚阿片类激动剂治疗(即μ-阿片受体完全激动剂美沙酮和部分激动剂丁丙诺啡)对呼吸功能可能有何影响。然而,已有文献记载美沙酮维持药物治疗中存在睡眠呼吸紊乱,并且有新证据表明丁丙诺啡和丁丙诺啡 - 纳洛酮维持治疗中也存在类似的睡眠呼吸紊乱。
为丁丙诺啡 - 纳洛酮维持药物治疗中出现的睡眠呼吸紊乱提供进一步的临床证据。
作者报告另外两例睡眠呼吸紊乱病例,这两名患有严重阿片类药物使用障碍的患者,作为门诊患者接受丁丙诺啡 - 纳洛酮维持治疗并取得成功。两名患者均书面同意将其临床信息纳入本病例报告,并对其身份信息进行了保密处理。
两名成年女性患者在丁丙诺啡 - 纳洛酮维持治疗中病情稳定,但出现白天嗜睡症状,经转诊评估发现存在睡眠呼吸紊乱。一名患者通过减少丁丙诺啡 - 纳洛酮及其他镇静药物剂量并开始使用持续气道正压通气(CPAP)设备后,白天嗜睡症状有所改善。然而,另一名患者无法耐受丁丙诺啡 - 纳洛酮剂量减少和/或启动CPAP,其白天嗜睡症状持续存在。
丁丙诺啡 - 纳洛酮维持治疗可能与睡眠呼吸紊乱有关。在丁丙诺啡 - 纳洛酮治疗本身的影响、同时存在的疾病(如肥胖和吸烟)或其他药物的影响,或它们的某种组合中,很难区分睡眠呼吸紊乱的原因。无论病因如何,睡眠呼吸紊乱及其后果给正在从阿片类药物使用障碍中康复的患者带来了独特的挑战,因此需要仔细评估和管理。