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先天性完全性心脏传导阻滞

Congenital complete heart block.

作者信息

Agarwala B, Sheikh Z, Cibils L A

机构信息

Department of Pediatrics, University of Chicago, Illinois, USA.

出版信息

J Natl Med Assoc. 1996 Nov;88(11):725-9.

Abstract

Congenital complete heart block in utero has become diagnosed more frequently with the clinical use of fetal echocardiography. The fetus with complete heart block may remain asymptomatic or may develop congestive heart failure. Congenital complete heart block is more frequently seen in infants of mothers with systemic lupus erythematosus, both clinically manifested and subclinical systemic lupus erythematosus with positive antibodies (SS-A and SS-B antibodies). At birth, the neonate with complete heart block may remain asymptomatic and may not require a pacemaker to increase the heart rate. The indications for a pacemaker in neonates with complete heart block have been discussed. Both in-utero and neonatal management of congenital complete heart block are discussed to manage congestive heart failure in a fetus. Four patients with congenital complete heart block are presented covering a broad spectrum of clinical presentation, diagnosis, and management both in the fetal and neonatal period.

摘要

随着胎儿超声心动图在临床上的应用,子宫内先天性完全性心脏传导阻滞的诊断越来越频繁。患有完全性心脏传导阻滞的胎儿可能无症状,也可能发展为充血性心力衰竭。先天性完全性心脏传导阻滞在患有系统性红斑狼疮的母亲所生婴儿中更为常见,包括临床表现为系统性红斑狼疮和抗体(SS - A和SS - B抗体)阳性的亚临床系统性红斑狼疮。出生时,患有完全性心脏传导阻滞的新生儿可能无症状,可能不需要起搏器来提高心率。已经讨论了完全性心脏传导阻滞新生儿使用起搏器的指征。本文讨论了先天性完全性心脏传导阻滞在子宫内和新生儿期的管理,以处理胎儿的充血性心力衰竭。介绍了4例先天性完全性心脏传导阻滞患者,涵盖了胎儿期和新生儿期广泛的临床表现、诊断和管理情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8191/2608175/72cf6bfb57a5/jnma00388-0066-a.jpg

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