大动脉转位逆位合并先天性完全性心脏传导阻滞:初始处理和涉及一个特殊单位

Kunlayanut Kanjanabura, Kanjanabura Jongyorklang, Watcharada Uckara, E. Surakarn, Thavatchai Sasiprapha
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引用次数: 0

摘要

本文报道1例足月女新生儿,孕周40周(超声)产前诊断为胎位倒置和左心瓣。产前检测到大动脉转位(TGA)和不规则胎儿心动过缓。出生后立即,心电图(ECG)监测显示一个完整的心脏传导阻滞,没有血流动力学妥协的迹象。患者随后被转移到新生儿重症监护病房(NICU)进行呼吸支持。进行密切观察和进一步超声心动图检查。该患者在4天大时被空运到诗丽吉王后国立儿童保健研究所接受心血管疾病的最终治疗。本文介绍了如何克服运输一个非常年轻的新生儿复杂的心脏问题的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transposition of The Great Arteries, Situs Inversus with Congenital Complete Heart Block: Initial Management and Referring to a Special Unit
A case of a term female newborn, 40-week gestational age (by ultrasound (US)) with prenatal diagnosis of situs inversus and levocardia is reported. Transposition of the great arteries (TGA) and irregular fetal bradycardia were prenatally detected. Immediately after birth, electrocardiogram (ECG) monitoring revealed a complete heart block with no sign of hemodynamic compromise. The patient was then transferred to the neonatal intensive care unit (NICU) for ventilatory support. Close observation and further investigation with echocardiogram were undertaken. The patient was transferred by air at the age of 4 days to the Queen Sirikit National Institute of Child Health for definitive cardiovascular treatments. This paper describes how to overcome the challenges of transporting a very young neonate with complex cardiac problems.
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