使用氧饱和度≥3%或唤醒定义的低通气,研究阻塞性睡眠呼吸暂停的长期全因死亡率风险。

Rohit Budhiraja, Stuart F Quan
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引用次数: 0

摘要

研究目的:之前的一些研究表明,阻塞性睡眠呼吸暂停(OSA)导致的死亡率增加,而 OSA 的定义要求氧饱和度至少达到 4% 才能确定呼吸暂停。目前还没有基于社区的大型研究确定OSA长期死亡的风险,OSA的低通气定义为≥3%的氧气饱和度或唤醒(AHI3%A):方法:对5591名睡眠心脏健康研究参与者的数据进行了分析,这些参与者基线时没有流行性心血管疾病,并接受了多导睡眠图检查,其OSA诊断采用AHI3%A标准,全因死亡率平均随访时间为10.9±3.2年:结果:在随访期间,该组共有 1050 人死亡。Kaplan-Meir 存活率图显示,随着 AHI 严重程度的增加,存活率也随之降低。在调整年龄、性别、种族、体重指数、胆固醇、高密度脂蛋白、自我报告的高血压和/或糖尿病以及吸烟状况后,Cox 比例危险回归模型显示,随着 AHI 的增加,全因死亡风险显著增加,危险比 (HR, 95% CI) 为 1.13 (1.04-1.23)。在分类模型中,严重 OSA 患者的死亡风险明显更高[调整后 HR 1.38(1.09-1.76)]。当按性别或年龄分层时,严重 OSA 会增加男性的死亡风险[调整后 HR 1.14 (1.01-1.28)],结论也是如此:严重 AHI3%A OSA 与死亡风险显著增加有关,尤其是男性和以下人群
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term All-Cause Mortality Risk in Obstructive Sleep Apnea Using Hypopneas Defined by a ≥3 Percent Oxygen Desaturation or Arousal.

Study objectives: Some prior studies have demonstrated an increase in mortality associated with obstructive sleep apnea (OSA) utilizing a definition of OSA that requires a minimum 4% oxygen desaturation to identify a hypopnea. No large community-based studies have determined the risk of long-term mortality with OSA with hypopneas defined by a ≥3% O2 desaturation or arousal (AHI3%A).

Methods: Data from 5591 Sleep Heart Health Study participants without prevalent cardiovascular disease at baseline who underwent polysomnography were analyzed regarding OSA diagnosed using the AHI3%A criteria and all-cause mortality over a mean follow up period of 10.9±3.2 years.

Results: There were 1050 deaths in this group during the follow-up period. A Kaplan-Meir plot of survival revealed a reduction in survival with increasing AHI severity. Cox proportional hazards regression models revealed significantly increased all-cause mortality risk with increasing AHI, hazard ratio (HR, 95% CI) 1.13 (1.04-1.23), after adjusting for age, sex, race, BMI, cholesterol, HDL, self-reported hypertension and/or diabetes and smoking status. In categorical models, the mortality risk was significantly higher with severe OSA [adjusted HR 1.38 (1.09-1.76)]. When stratified by gender or age, severe OSA was associated with increased risk of death in men [adjusted HR 1.14 (1.01-1.28)] and in those <70 years of age [adjusted HR 1.51 (1.02-2.26)]. In contrast, AHI severity was not associated with increased mortality in women or those ≥70 years of age in fully adjusted models.

Conclusion: Severe AHI3%A OSA is associated with significantly increased mortality risk, especially in men and those <70 years of age.

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