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成人艾森曼格综合征患者心源性猝死的决定因素。

Determinants of Sudden Cardiac Death in Adult Patients With Eisenmenger Syndrome.

机构信息

Departments of Cardiovascular Diseases Mayo Clinic Jacksonville FL.

Department of Cardiovascular Diseases Mayo Clinic Rochester MN.

出版信息

J Am Heart Assoc. 2020 Mar 17;9(6):e014554. doi: 10.1161/JAHA.119.014554. Epub 2020 Mar 15.

Abstract

Background Patients with Eisenmenger syndrome are known to have a high incidence of sudden cardiac death (SCD), yet the underlying causes are not well understood. We sought to define the predictors of SCD in this population. Methods and Results A retrospective analysis of all patients with Eisenmenger syndrome from 2 large tertiary referral centers was performed. ECGs, prolonged ambulatory recordings, echocardiograms, and clinical histories were reviewed; and the cause of death was identified. A total of 246 patients (85 [34.6%] men) with a mean age of 37.3 (±14.2) years were followed up for a median of 7 years. Over the study period, 136 patients died, with 40 experiencing SCD and 74 experiencing cardiac death (sudden and nonsudden). Age, atrial fibrillation, prolonged QRS duration, complete heart block, right atrial enlargement, right bundle branch block, increased right atrial pressure, impaired biventricular function, and the presence of a pacemaker were associated with increased risk of SCD, whereas advanced pulmonary hypertension therapies were protective. Atrial fibrillation (11.45-fold increased risk; <0.001) and QRS duration ≥120 ms (2.06-fold increased risk; =0.034) remained significant predictors of SCD in the multivariate analysis, whereas advanced pulmonary hypertension therapies were strongly protective against SCD (<0.001). Conclusions Atrial arrhythmias, impaired ventricular function, and conduction system disease were associated with increased risk of SCD in this cohort of patients with Eisenmenger syndrome, providing an opportunity for early risk stratification and potential intervention. Clinical heart failure symptoms (New York Heart Association class ≥II) were predictive of increased mortality but not of SCD, suggesting a potential arrhythmic cause behind SCD.

摘要

背景

已知艾森曼格综合征患者发生心源性猝死(SCD)的发生率较高,但发病原因尚不清楚。我们旨在确定该人群中 SCD 的预测因素。

方法和结果

对来自 2 个大型三级转诊中心的所有艾森曼格综合征患者进行了回顾性分析。回顾了心电图、长时间动态心电图记录、超声心动图和临床病史;并确定了死亡原因。共纳入 246 例患者(85 例[34.6%]为男性),平均年龄为 37.3(±14.2)岁,中位随访时间为 7 年。研究期间,136 例患者死亡,其中 40 例发生 SCD,74 例发生心脏性死亡(猝死和非猝死)。年龄、心房颤动、QRS 时限延长、完全性心脏阻滞、右心房增大、右束支传导阻滞、右心房压升高、双心室功能障碍以及起搏器的存在与 SCD 风险增加相关,而晚期肺动脉高压治疗具有保护作用。在多变量分析中,心房颤动(风险增加 11.45 倍;<0.001)和 QRS 时限≥120ms(风险增加 2.06 倍;=0.034)仍然是 SCD 的显著预测因素,而晚期肺动脉高压治疗对 SCD 具有强烈的保护作用(<0.001)。

结论

在该队列中,心房心律失常、心室功能障碍和传导系统疾病与 SCD 风险增加相关,为早期风险分层和潜在干预提供了机会。心力衰竭临床症状(纽约心脏协会分级≥II 级)预测死亡率增加,但不预测 SCD,提示 SCD 背后可能存在心律失常原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f9/7335528/38b5e1f5cc43/JAH3-9-e014554-g001.jpg

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