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. 2026 Jan 2;64(1):95-98.
doi: 10.3760/cma.j.cn112140-20250814-00754.

[Clinical characteristics analysis of 6 children with anomalous origin of coronary artery supported by extracorporeal membrane oxygenation]

[Article in Chinese]
Affiliations

[Clinical characteristics analysis of 6 children with anomalous origin of coronary artery supported by extracorporeal membrane oxygenation]

[Article in Chinese]
D L Cheng et al. Zhonghua Er Ke Za Zhi. .

Abstract

Objective: To summarize the clinical features of children with anomalous origin of coronary artery (AOCA) who received extracorporeal membrane oxygenation (ECMO) support. Methods: A case series study was conducted. Clinical data was collected from 6 children who were diagnosed with AOCA by coronary computed tomography angiography or digital subtraction angiography and received ECMO support in the Pediatric Intensive Care Unit of Henan Provincial People's Hospital between January 2020 and August 2024. Descriptive analysis was performed on their clinical features, laboratory test results, point-of-care echocardiography results, imaging findings, surgical management, and outcomes. Results: Among the 6 children (3 males and 3 females), the age of onset was 12.5 (11.0, 13.0) years. All 6 patients were transported from other hospitals under ECMO support. Five patients were admitted with chief complaints of "cardiac arrest after strenuous activity, syncope after strenuous activity, or heart failure" and were initially diagnosed with fulminant myocarditis or cardiomyopathy. All 6 children had significantly elevated troponin and B-type natriuretic peptide levels upon admission. Point-of-care echocardiography revealed segmental left ventricular systolic dysfunction in all 6 children, and AOCA was detected in 2 cases based on bedside ultrasound. ECMO was successfully weaned in 5 children. All 6 cases were diagnosed with AOCA. Four children underwent surgical coronary artery correction, one received a heart transplantation, and one missed the optimal window for surgical correction. Heart transplantation was recommended for the latter, but the parents declined, and the patient was discharged. During the follow-up until August 2025, all 6 children survived. Conclusions: AOCA in children is prone to misdiagnosis as other diseases in the early stage. Timely ECMO support provides the possibility of surgery or heart transplantation for children experiencing acute ischemic and hypoxic episodes due to AOCA, improving survival rates.

目的: 总结冠状动脉起源异常并接受体外膜氧合(ECMO)支持患儿的临床特征。 方法: 病例系列研究。收集2020年1月至2024年8月河南省人民医院儿童重症监护病房收治的6例由心脏冠状动脉CT血管造影或者数字减影血管造影技术确诊为儿童冠状动脉起源异常行ECMO支持患儿的临床病例资料,对其临床特征、实验室检验结果、床旁超声心动图结果、影像学检查结果、手术治疗方案及转归情况等进行描述性分析。 结果: 6例患儿中男3例、女3例,起病年龄为12.5(11.0,13.0)岁。6例患儿均为ECMO院间转运患儿,5例以“剧烈活动后心搏骤停或者剧烈活动后晕厥、心力衰竭”为主诉入院,初步诊断为暴发性心肌炎或者心肌病;6例患儿入院肌钙蛋白、B型脑钠肽均明显升高,6例患儿床旁超声心动图均提示左心室节段性收缩功能障碍,床旁超声发现冠状动脉起源异常2例。ECMO成功撤机5例。6例冠状动脉起源异常患儿中,4例接受外科冠状动脉矫正手术治疗,1例接受心脏移植,1例患儿失去矫正手术时机,建议心脏移植治疗,家长拒绝后出院。随访至2025年8月,6例患儿均存活。 结论: 儿童冠状动脉起源异常早期易误诊为其他疾病,及时的ECMO支持为儿童冠状动脉起源异常患儿急性缺血缺氧发作提供了手术或者心脏移植的可能,提高了存活率。.

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