新生儿转位合并肥厚性心肌病和持续性肺动脉高压

IF 1 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2022-05-23 DOI:10.1177/21501351221098135

B. Brooks, A. Krishnan, Y. D'udekem, Gregory K. Yurasek

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引用次数: 0

摘要

同时出现大动脉转位和肥厚性心肌病是罕见的，并使最佳手术时机复杂化。我们报告了一个新生儿转位和严重肥厚性心肌病，产后病程合并持续性肺动脉高压，在生命的第一天接受体外膜氧合支持，直到成功的动脉转换手术8。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Transposition With Hypertrophic Cardiomyopathy and Persistent Pulmonary Hypertension of the Newborn

The contemporaneous presentation of transposition of the great arteries and hypertrophic cardiomyopathy is rare and complicates optimal surgical timing. We present a newborn with transposition and severe hypertrophic cardiomyopathy with a postnatal course complicated by persistent pulmonary hypertension who was supported with extracorporeal membrane oxygenation until successful arterial switch operation on the day of life 8.

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来源期刊

World Journal for Pediatric and Congenital Heart Surgery CARDIAC & CARDIOVASCULAR SYSTEMS-

CiteScore

1.80

自引率

11.10%

发文量

128