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胎儿完全性心脏传导阻滞。

Fetal complete heart block.

作者信息

Machado M V, Tynan M J, Curry P V, Allan L D

机构信息

Department of Perinatal Cardiology, Guy's Hospital, London.

出版信息

Br Heart J. 1988 Dec;60(6):512-5. doi: 10.1136/hrt.60.6.512.

DOI:10.1136/hrt.60.6.512
PMID:3224055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1224893/
Abstract

In a series of over 6000 patients referred for fetal echocardiography during an eight year period, 37 fetuses were found to have complete heart block. There were 16 cases of isolated heart block and 21 cases associated with structural heart disease. All mothers of fetuses with isolated complete heart block had evidence of circulating syndrome Sjögren A antibody (Ro). Only one mother had clinical evidence of connective tissue disease. In the 21 cases associated with structural heart disease there were 17 cases of atrioventricular septal defect, one case of secundum atrial and perimembranous ventricular septal defects, two cases of tetralogy of Fallot, and one case of pulmonary stenosis. All fetuses with atrioventricular septal defects and complete heart block had left atrial isomerism. Additional abnormalities of the great arteries were often found in this group; these were double outlet right ventricle, transposition of the great arteries, pulmonary atresia, coarctation of aorta, and stenosis of the pulmonary or aortic valves. Intrauterine congestive heart failure was a feature of four cases in the group with isolated complete heart block and 11 cases of the group with associated structural heart disease. The outcome in the fetuses with isolated complete heart block was better than in those with heart disease: 12 of the 16 fetuses are alive, two of them have a pacemaker. But only three of the group of 21 fetuses with cardiac malformation are alive, and two of them have a pacemaker.

摘要

在为期八年的时间里,超过6000名患者接受了胎儿超声心动图检查,其中37例胎儿被发现患有完全性心脏传导阻滞。有16例孤立性心脏传导阻滞病例和21例与结构性心脏病相关的病例。所有患有孤立性完全性心脏传导阻滞胎儿的母亲都有循环综合征干燥综合征A抗体(Ro)的证据。只有一位母亲有结缔组织病的临床证据。在21例与结构性心脏病相关的病例中,有17例房室间隔缺损,1例继发孔型房间隔缺损和膜周部室间隔缺损,2例法洛四联症,1例肺动脉狭窄。所有患有房室间隔缺损和完全性心脏传导阻滞的胎儿均有左心房异构。该组中常发现大动脉的其他异常;这些是右心室双出口、大动脉转位、肺动脉闭锁、主动脉缩窄以及肺动脉或主动脉瓣狭窄。宫内充血性心力衰竭是孤立性完全性心脏传导阻滞组中的4例以及伴有结构性心脏病组中的11例的特征。孤立性完全性心脏传导阻滞胎儿的预后优于患有心脏病的胎儿:16例胎儿中有12例存活,其中2例有起搏器。但21例患有心脏畸形的胎儿组中只有3例存活,其中2例有起搏器。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa5/1224893/434639411c14/brheartj00084-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa5/1224893/434639411c14/brheartj00084-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa5/1224893/434639411c14/brheartj00084-0055-a.jpg

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