终末期肾病患者的睡眠呼吸暂停:对心血管和神经系统预后的影响。

L Acree, J L Waller, W B Bollag, W J Healy, S L Baer, V Taskar
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引用次数: 0

摘要

简介:睡眠呼吸暂停(SA)是终末期肾病(ESRD)患者的一个重要合并症。睡眠呼吸暂停与心脏和神经系统疾病之间的关系众所周知。本研究调查了 ESRD 患者中 SA 与心血管和脑血管预后之间的关系:在一项回顾性队列研究中,我们查询了美国肾脏数据系统,以确定 2005 年至 2013 年期间开始血液透析的 18-100 岁 ESRD 患者。SA诊断和临床合并症是根据《国际疾病分类-9》代码确定的。人口统计学变量来自美国医疗保险和医疗补助服务中心的 2728 号表格。在控制人口统计学和临床变量的情况下,采用逻辑回归法检测 SA 与心肌梗死(MI)或中风的关联:在 858,131 名符合纳入标准的受试者中,587 人患有中枢性 SA,22,724 人患有阻塞性 SA。与非 SA 患者相比,SA 患者更年轻,更可能是男性和白种人。SA患者中吸烟和酗酒、高血压、心力衰竭和糖尿病患者也较多。中枢性 SA(aRR = 1.69,95% CI = 1.28-2.23)和阻塞性 SA(aRR = 1.15,95% CI = 1.09-1.21)与中风风险增加有关,但与 MI 无关:结论:在 ESRD 患者中,诊断出中枢性 SA 或阻塞性 SA 会增加中风风险,但不会增加心肌梗死风险。在 ESRD 患者中,早期识别和治疗 SA 可能有助于降低这些患者的中风风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep apnea in end-stage renal disease patients: Impact on cardiovascular and neurological outcomes.

Introduction: Sleep apnea (SA) is an important comorbidity in end-stage renal disease (ESRD) patients. The association between SA and cardiac and neurological disease is known. This study investigates the relationship between SA and cardiovascular and cerebrovascular outcomes in the ESRD population.

Methods: In a retrospective cohort study, the United States Renal Data System was queried to identify ESRD patients aged 18-100 years in whom hemodialysis had been initiated between 2005 and 2013. Diagnoses of SA and clinical comorbidities were determined from International Classification of Disease-9 codes. Demographic variables were obtained from Centers for Medicare and Medicaid Services Form-2728. Logistic regression was used to examine the association of SA with myocardial infarction (MI) or with stroke, controlling for demographic and clinical variables.

Results: Of 858,131 subjects meeting the inclusion criteria, 587 had central SA, and 22,724 had obstructive SA. The SA cohort was younger, more likely to be male and Caucasian compared to the non-SA cohort. Patients with SA also had more tobacco and alcohol use, hypertension, heart failure, and diabetes. Central SA (aRR = 1.69, 95% CI = 1.28-2.23) and obstructive SA (aRR = 1.15, 95% CI = 1.09-1.21) were associated with an increased risk of stroke but not MI.

Conclusion: In the ESRD population, a diagnosis of central SA or obstructive SA increased the risk of stroke, but not MI. Early identification and treatment of SA in the ESRD population may help reduce the risk of stroke in these patients.

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