Evidence map›Paper›PMID 39020323›Full record

ArticleBMC cardiovascular disorders2024

An unusual cause of cardiac arrest in a young infant.

Yuhao Wu, Siyi Che, Yonggang Li

Abstract readCase Reports
In one paragraph

Article in BMC cardiovascular disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yuhao WuDepartment of Cardiothoracic Surgery, Children's Hospital of Chongqing Medical University, Chongqing, China.
Siyi CheMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Chongqing, China.
Yonggang LiDepartment of Cardiothoracic Surgery, Children's Hospital of Chongqing Medical University, Chongqing, China. 485659@hospital.cqmu.edu.cn.

Funding

Chongqing Postdoctoral Research Project Special Support 2023CQBSHTB3074CQMU Program for Youth Innovation in Future Medicine, 2022 W0204Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission CSTB2023NSCQ-BHX0010
6 · The paper itself

Abstract

backgroundAnomalous aortic origin of a coronary artery from the inappropriate sinus of Valsalva (AAOCA) is a rare congenital heart lesion. It is uncommon for patients with AAOCA to present with severe symptoms at a very young age. CASE PRESENTATION: We describe a very rare but critical presentation in a young infant with AAOCA that requires surgical repair and pacemaker placement. A three-month-old infant was referred because of syncope. Cardiac arrest occurred shortly after admission. The electrocardiogram indicated a complete atrioventricular block and a transvenous temporary pacemaker was implanted. A further coronary computed tomographic angiography (CTA) showed the anomalous origin of the right coronary artery from the left sinus of Valsalva. Coronary artery unroofing was performed due to an interarterial course with the intramural component, and a permanent epicardial pacemaker was implanted. The postoperative recovery was uneventful, and this patient was thriving and asymptomatic at the nine-month follow-up. However, the electrocardiogram still indicated a complete pacing rhythm.

conclusionsBy timely diagnosis and treatment, this patient is successfully rescued. Although rare, AAOCA may be fatal even in infants.

Indexed as

Cardiac Pacing, ArtificialCoronary Vessel AnomaliesPacemaker, ArtificialAtrioventricular BlockComputed Tomography AngiographyCoronary AngiographyElectrocardiographyHeart ArrestHumansInfantMaleSinus of ValsalvaTreatment OutcomeAnomalous coronary arteryCardiac arrestInfant

Identifiers

PMID39020323
PMCPMC11253404

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.