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无顶冠状静脉窦及冠状静脉窦口闭锁。对复杂先天性心脏病治疗的启示。

Unroofed coronary sinus and coronary sinus orifice atresia. Implications for management of complex congenital heart disease.

作者信息

Adatia I, Gittenberger-de Groot A C

机构信息

Department of Paediatric Cardiology, Universitätskinderklinik, Freiburg, Germany.

出版信息

J Am Coll Cardiol. 1995 Mar 15;25(4):948-53. doi: 10.1016/0735-1097(94)00475-6.

Abstract

OBJECTIVES

The aim of this study was to assess the morphology of the coronary sinus, its drainage and associated cardiac malformations when there is either complete unroofing of the coronary sinus or atresia of its connection to the right atrium.

BACKGROUND

As more children with complex cardiac anomalies are accepted for primary surgical repair or palliation with cavopulmonary anastomoses, a knowledge of coronary sinus and systemic venous anomalies is important if coronary venous return is to be preserved and residual shunts avoided.

METHODS

Twenty-six heart-lung specimens without a coronary sinus draining to the right atrium were identified from the Leiden collection of congenital heart malformations. These were classified into specimens with an unroofed coronary sinus and those with atresia of the coronary sinus orifice. Attention was paid to the associated cardiac malformations.

RESULTS

In 14 (54%; confidence limits [CL] 35%, 73%) of 26 specimens, there was an unroofed coronary sinus, associated with persistence of the left superior caval vein. An inferoposterior location of an atrial septal defect was detected in 2 (14%; CL -4%, 33%) of 14. Atrial appendage anomalies were seen in 13 (93%; CL 79%, 106%) of 14 specimens, exemplified by both right and left isomerism. These were frequently associated with an atrioventricular septal defect (12 [86%; CL 67%, 104%] of 14). An atretic coronary sinus orifice was seen in 12 (46%; CL 27%, 65%) of 26. Atrial appendage anomalies (2 [17%; CL -4%, 38%] of 12) were rare in these cases. The drainage was then by way of a left superior caval vein or, in its absence, a coronary sinus to left atrial window. Ventricular hypoplasia was seen in both categories of coronary sinus abnormalities. Important ventricular hypoplasia was seen in 12 cases (46%; CL 27%, 65%).

CONCLUSIONS

These findings emphasize the need to study coronary sinus drainage before procedures such as ligation or transcatheter coil embolization of a left superior caval vein, venous redirection or closure of a dorsal atrial septal defect are contemplated. These procedures might inadvertently lead to impairment of coronary venous return or persistence of an intracardiac shunt.

摘要

目的

本研究旨在评估冠状静脉窦完全未闭或其与右心房连接闭锁时冠状静脉窦的形态、引流情况及相关心脏畸形。

背景

随着越来越多患有复杂心脏畸形的儿童接受一期手术修复或采用腔肺吻合术进行姑息治疗,若要保留冠状静脉回流并避免残余分流,了解冠状静脉窦和体静脉异常情况至关重要。

方法

从莱顿先天性心脏畸形标本库中识别出26例无冠状静脉窦引流至右心房的心肺标本。这些标本被分为冠状静脉窦未闭标本和冠状静脉窦口闭锁标本。关注相关的心脏畸形。

结果

26例标本中有14例(54%;置信区间[CL]35%,73%)存在冠状静脉窦未闭,伴有左上腔静脉持续存在。14例中有2例(14%;CL -4%,33%)检测到房间隔缺损位于下后部。14例标本中有13例(93%;CL 79%,106%)可见心房附件异常,以左右异构为例。这些情况常与房室间隔缺损相关(14例中有12例[86%;CL 67%,104%])。26例中有12例(46%;CL 27%,65%)可见冠状静脉窦口闭锁。这些病例中,心房附件异常较少见(12例中有2例[17%;CL -4%,38%])。然后引流通过左上腔静脉进行,若左上腔静脉不存在,则通过冠状静脉窦至左心房窗口。在两类冠状静脉窦异常中均可见心室发育不全。12例(46%;CL 27%,65%)可见严重的心室发育不全。

结论

这些发现强调在考虑诸如结扎或经导管线圈栓塞左上腔静脉、静脉改道或闭合背侧房间隔缺损等手术之前,有必要研究冠状静脉窦引流情况。这些手术可能会无意中导致冠状静脉回流受损或心内分流持续存在。

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