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肺动脉起源异常左冠状动脉患儿就诊时及随访期间的心电图变化:一项多中心分析

Electrocardiographic Changes at Presentation and Over Time in Children with Anomalous Left Coronary Artery from the Pulmonary Artery: A Multicenter Analysis.

作者信息

Amula Venu, Radman Monique, Loomba Rohit S, Kwiatkowski David M, Beshish Asaad, Flores Saul, Bakar Adnan M, Capone Christine A, Suguna Narasimhulu Sukumar, Pizzuto Matthew F, Karki Karan B, Cashen Katherine, Niu Mary C, Mastropietro Christopher W

机构信息

University of Utah School of Medicine, Salt Lake City, UT, USA.

Division of Critical Care, Department of Pediatrics, University of Utah, 295 Chipeta Way, Salt Lake City, UT, USA.

出版信息

Pediatr Cardiol. 2025 May 31. doi: 10.1007/s00246-025-03901-w.

Abstract

Multicenter studies describing electrocardiogram (ECG) patterns in children presenting with anomalous left coronary artery from the pulmonary artery (ALCAPA), to our knowledge, have not been published. This study aimed to describe the ECG findings at presentation and over time in a multicenter cohort of children with ALCAPA and assess their association with clinical outcomes. We performed a retrospective ECG analysis of 188 patients with ALCAPA who presented between 1/2009 and 3/2018 at 21 centers affiliated with Collaborative Research for the Pediatric Cardiac Intensive Care Society. ECGs were categorized apriori as Classic (pathologic Q waves in anterolateral leads), non-classic (abnormal but without pathologic Q waves), and normal. The primary outcome was major adverse cardiac events (MACE) following ALCAPA repair, defined as extracorporeal support, cardiopulmonary resuscitation, heart transplantation, or death. Classic, non-classic, and normal ECG findings were seen at presentation in 124 (66%), 49 (26%), and 15 (8%) patients, respectively. There was no association between ECG category and MACE. Patients with non-classic or normal ECG findings were significantly more likely to present with normal or mildly diminished left ventricular systolic function and had significantly shorter duration of ventilation and hospital stay. Among 70 patients with ECGs at ~ 3 years following surgery, classic, non-classic, and normal ECG patterns were seen in 6 (8%), 29 (41%), and 35 (50%) patients, respectively. In conclusion, one-third of patients with ALCAPA presented with non-Classic or normal ECG patterns, and these patients were more likely to have preserved cardiac function and recover more quickly following surgical repair.

摘要

据我们所知,尚未发表过描述患有肺动脉起源异常左冠状动脉(ALCAPA)儿童心电图(ECG)模式的多中心研究。本研究旨在描述多中心队列中患有ALCAPA儿童就诊时及随访期间的心电图表现,并评估其与临床结局的关联。我们对2009年1月至2018年3月期间在小儿心脏重症监护协会协作研究下属21个中心就诊的188例ALCAPA患者进行了回顾性心电图分析。心电图预先分为典型(前侧壁导联病理性Q波)、非典型(异常但无病理性Q波)和正常三类。主要结局是ALCAPA修复术后的主要不良心脏事件(MACE),定义为体外支持、心肺复苏、心脏移植或死亡。就诊时,分别有124例(66%)、49例(26%)和15例(8%)患者出现典型、非典型和正常心电图表现。心电图类别与MACE之间无关联。非典型或正常心电图表现的患者更有可能表现为左心室收缩功能正常或轻度降低,通气时间和住院时间明显缩短。在术后约3年有心电图记录的70例患者中,分别有6例(8%)、29例(41%)和35例(50%)出现典型、非典型和正常心电图模式。总之,三分之一的ALCAPA患者表现为非典型或正常心电图模式,这些患者更有可能保留心脏功能,手术修复后恢复更快。

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