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慢性疼痛患者使用阿片类药物时发生睡眠呼吸暂停的预测因素。

Predictive factors for sleep apnoea in patients on opioids for chronic pain.

机构信息

Department of Anesthesia and Pain Medicine, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada.

Department of Anesthesia, Women's College Hospital, University of Toronto, Toronto, On, Canada.

出版信息

BMJ Open Respir Res. 2019 Dec 23;6(1):e000523. doi: 10.1136/bmjresp-2019-000523. eCollection 2019.

Abstract

BACKGROUND

The risk of death is elevated in patients taking opioids for chronic non-cancer pain. Respiratory depression is the main cause of death due to opioids and sleep apnoea is an important associated risk factor.

METHODS

In chronic pain clinics, we assessed the STOP-Bang questionnaire (a screening tool for sleep apnoea; noring, iredness, bserved apnoea, high blood ressure, ody mass index, age, neck circumference and male gender), Epworth Sleepiness Scale, thyromental distance, Mallampati classification, daytime oxyhaemoglobin saturation (SpO) and calculated daily morphine milligram equivalent (MME) approximations for each participant, and performed an inlaboratory polysomnogram. The primary objective was to determine the predictive factors for sleep apnoea in patients on chronic opioid therapy using multivariable logistic regression models.

RESULTS

Of 332 consented participants, 204 underwent polysomnography, and 120 (58.8%) had sleep apnoea (AHI ≥5) (72% obstructive, 20% central and 8% indeterminate sleep apnoea), with a high prevalence of moderate (23.3%) and severe (30.8%) sleep apnoea. The STOP-Bang questionnaire and SpO are predictive factors for sleep apnoea (AHI ≥15) in patients on opioids for chronic pain. For each one-unit increase in the STOP-Bang score, the odds of moderate-to-severe sleep apnoea (AHI ≥15) increased by 70%, and for each 1% SpO decrease the odds increased by 33%. For each 10 mg MME increase, the odds of Central Apnoea Index ≥5 increased by 3%, and for each 1% SpO decrease the odds increased by 45%.

CONCLUSION

In patients on opioids for chronic pain, the STOP-Bang questionnaire and daytime SpO are predictive factors for sleep apnoea, and MME and daytime SpO are predictive factors for Central Apnoea Index ≥5.

TRIAL REGISTRATION NUMBER

NCT02513836.

摘要

背景

慢性非癌性疼痛患者服用阿片类药物会增加死亡风险。呼吸抑制是阿片类药物致死的主要原因,而睡眠呼吸暂停是一个重要的相关危险因素。

方法

在慢性疼痛诊所,我们评估了 STOP-Bang 问卷(一种用于睡眠呼吸暂停的筛查工具;打鼾、疲劳、观察到的呼吸暂停、高血压、体质量指数、年龄、颈围和男性性别)、Epworth 嗜睡量表、甲状软骨下距离、Mallampati 分类、白天血氧饱和度(SpO)并为每位参与者计算了每日吗啡毫克当量(MME)近似值,并进行了实验室多导睡眠图检查。主要目的是使用多变量逻辑回归模型确定慢性阿片类药物治疗患者睡眠呼吸暂停的预测因素。

结果

在 332 名同意参与的患者中,有 204 名接受了多导睡眠图检查,其中 120 名(58.8%)患有睡眠呼吸暂停(AHI≥5)(72%为阻塞性,20%为中枢性,8%为不确定型睡眠呼吸暂停),中重度(23.3%)和重度(30.8%)睡眠呼吸暂停的患病率较高。STOP-Bang 问卷和 SpO 是阿片类药物治疗慢性疼痛患者睡眠呼吸暂停(AHI≥15)的预测因素。STOP-Bang 评分每增加 1 分,中重度睡眠呼吸暂停(AHI≥15)的几率增加 70%,SpO 每降低 1%,几率增加 33%。MME 每增加 10mg,中枢性呼吸暂停指数(Central Apnoea Index)≥5 的几率增加 3%,SpO 每降低 1%,几率增加 45%。

结论

在慢性疼痛接受阿片类药物治疗的患者中,STOP-Bang 问卷和白天 SpO 是睡眠呼吸暂停的预测因素,而 MME 和白天 SpO 是 Central Apnoea Index≥5 的预测因素。

试验注册

NCT02513836。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b9/6936992/9174cf2a2775/bmjresp-2019-000523f01.jpg

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