接受美沙酮治疗阿片类药物使用障碍患者的夜间睡眠和呼吸系统紊乱。

Journal of addictions nursing Pub Date : 2023-10-01 Epub Date: 2023-09-28 DOI:10.1097/JAN.0000000000000470
Myles Finlay, Julie A Erwin, Lillian Skeiky, Devon A Hansen, Matthew E Layton, Raymond Quock, Hans P A Van Dongen, Marian Wilson
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摘要

摘要:在美国,阿片类药物是导致药物过量死亡的主要原因。美沙酮被用作治疗阿片类药物使用障碍(MOUD)的药物,可以减少对药物的渴望,促进禁欲。然而,接受美沙酮MOUD治疗的个体通常会报告主观睡眠问题,并有因阿片类药物而患呼吸抑制的风险。我们调查了8名患者(6名女性,2名男性;年龄31-68岁)在接受基于美沙酮的MOUD治疗的前90天的夜间睡眠和呼吸功能。参与者接受了夜间心肺多导睡眠图检查。睡眠和呼吸变量采用描述性统计数据进行表征,以与年龄相似的健康成年人的参考数据进行比较。尽管参与者在床上的时间为8.1±0.3小时(平均值±SD),但他们的总睡眠时间仅为6.8±1.3小时。他们表现出更长的睡眠潜伏期和间歇性清醒。睡眠结构不规律,睡眠周期紊乱。与参考数据相比,参与者的N1睡眠量减少,N3睡眠量增加。参与者表现出呼吸抑制,平均呼吸暂停低通气指数为每小时16.5±8.9次。中枢性睡眠呼吸暂停占呼吸事件的69.1%±20.9%。75%的参与者观察到类似Cheyne Stokes的呼吸模式,包括30秒周期的三次中枢睡眠呼吸暂停。我们的研究结果表明,早期接受美沙酮MOUD治疗的患者会出现睡眠障碍和呼吸障碍。这种夜间生理变化可能会对健康产生严重的长期影响,并导致意外服药过量率。识别和治疗患有睡眠呼吸暂停的MOUD患者可以降低死亡风险。
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Nighttime Sleep and Respiratory Disturbances in Individuals Receiving Methadone to Treat Opioid Use Disorder.

Abstract: Opioids are a leading cause of drug overdose deaths in the United States. Methadone used as medication for opioid use disorder (MOUD) reduces drug cravings and promotes abstinence. However, individuals in methadone-based MOUD treatment commonly report subjective sleep complaints and are at risk for respiratory depression from opioids. We investigated nighttime sleep and respiratory function in eight individuals (six women, two men; ages 31-68 years) in their first 90 days of methadone-based MOUD treatment. Participants underwent overnight cardiorespiratory polysomnography. Sleep and respiratory variables were characterized with descriptive statistics for comparison to reference data from similarly aged healthy adults. Although participants spent 8.1 ± 0.3 hours (mean ± SD ) in bed, their total sleep time was only 6.8 ± 1.3 hours. They exhibited longer sleep latency and intermittent wakefulness. Sleep structure was irregular, with disrupted sleep cycles. Participants also displayed a decreased amount of N1 sleep and an increased amount of N3 sleep, compared with reference data. Participants showed respiratory depression, with an average apnea-hypopnea index of 16.5 ± 8.9 events per hour. Central sleep apneas comprised 69.1% ± 20.9% of the respiratory events. A Cheyne-Stokes-like breathing pattern, consisting of 30-second cycles of three central sleep apneas, was observed in 75% of participants. Our results suggest that individuals early in methadone-based MOUD treatment experience disordered sleep and respiratory disturbances. Such nighttime physiological changes may have serious long-term health consequences and contribute to unintended overdose rates. Identifying and treating MOUD individuals with sleep apnea could reduce risk of death.

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