Congenital Complete Heart Block Requiring Temporary Pacemaker Placement at Birth: A Case Report.

IF 1.1 Q3 ANESTHESIOLOGY
Karthi Murari, Clint Humpherys, Nathaniel Lata, Christian Taylor, Sanket Shah, Todd Glenski
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引用次数: 0

Abstract

Congenital heart block (CHB) is a rare congenital cardiac disease where disruption of the atrioventricular (AV) node results in cardiac conduction abnormalities. The majority of CHB cases are associated with neonatal lupus antibodies that are associated with autoimmune destruction and fibrosis of the AV node, most commonly resulting in a congenital complete heart block (CCHB). We report the case of a 23-year-old mother who was found to have a fetus with significant bradycardia at a 21-week anatomy ultrasound. Subsequent fetal echocardiograms demonstrated a third-degree heart block, and laboratory workup of the mother was positive for SSA antibodies. Successful care of the fetus required multidisciplinary coordination to ensure adequate antepartum care, successful delivery of the fetus, and proper cardiovascular management of the neonate after birth. We discuss etiologies of fetal bradycardia, proper imaging techniques to diagnose fetal cardiac abnormalities, and the management of a neonate with CCHB after birth. Lastly, we emphasize how adequate operating room preparation and multidisciplinary planning are essential for optimal outcomes during time-sensitive and high-risk operating room procedures.

先天性完全性心脏传导阻滞需要在出生时放置临时起搏器:一例报告。
先天性心脏传导阻滞(CHB)是一种罕见的先天性心脏病,由于房室结的破坏导致心脏传导异常。大多数CHB病例与新生儿狼疮抗体相关,狼疮抗体与自身免疫破坏和房室结纤维化相关,最常见的是导致先天性完全性心脏传导阻滞(CCHB)。我们报告的情况下,23岁的母亲谁被发现有一个胎儿与显著心动过缓在21周解剖超声。随后的胎儿超声心动图显示三度心脏传导阻滞,母亲的实验室检查为SSA抗体阳性。成功的胎儿护理需要多学科协调,以确保充分的产前护理,胎儿的成功分娩,以及出生后新生儿的适当心血管管理。我们讨论胎儿心动过缓的病因,正确的成像技术来诊断胎儿心脏异常,和新生儿出生后与CCHB的管理。最后,我们强调充分的手术室准备和多学科规划对于时间敏感和高风险手术室手术的最佳结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.60
自引率
14.30%
发文量
31
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