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法洛四联症胎儿产前超声心动图诊断的准确性及预后

Accuracy of prenatal echocardiographic diagnosis and prognosis of fetuses with conotruncal anomalies.

作者信息

Tometzki A J, Suda K, Kohl T, Kovalchin J P, Silverman N H

机构信息

Department of Pediatric Echocardiography, University of California, San Francisco 94143-0214, USA.

出版信息

J Am Coll Cardiol. 1999 May;33(6):1696-701. doi: 10.1016/s0735-1097(99)00049-2.

Abstract

OBJECTIVES

The purpose of the study was to determine the accuracy of the prenatal echocardiographic diagnosis and prognosis of fetuses with conotruncal anomalies.

BACKGROUND

The accuracy of prenatal echocardiographic diagnoses of cardiac lesions has been reported, but no previous reports specifically address fetal conotruncal anomalies.

METHODS

Medical records of 61 fetuses, in which a fetal diagnosis of a conotruncal anomaly was made, were reviewed. Disease entities included were tetralogy of Fallot (TOF), double outlet right ventricle (DORV), transposition of the great arteries (TGA), and truncus arteriosus (TA).

RESULTS

Fetal diagnosis was established at a median of 24.5 weeks' gestation. Termination of pregnancy was chosen in 31% (19/61) of cases. Postnatal assessment of the diagnosis was not obtained in 12 cases. Excluding two sets of conjoined twins, accurate prenatal diagnosis including definition of the great artery orientation was achieved in 36 of 47 cases (77%). Seven of 17 fetuses with DORV anatomy, of which 6 were thought to have a subpulmonary ventricular septal defect (VSD), had incorrect prenatal assessment of the great artery relationships. One fetus thought to show features of TA had aortic atresia with VSD and normal-sized left ventricle. Of the 42 pregnancies that continued, 15 had major extracardiac malformations and/or chromosomal abnormalities of which one died in utero with trisomy-13 and TA. A further nine died within the neonatal period. Among the 27 fetuses without a documented chromosomal or major extracardiac anomaly, 13 (48%) died. Overall, the survival rate beyond 28 days of life was 52% (22/42). In contrast, 75% (6/8) of fetuses with TOF, excluding the absent pulmonary valve syndrome, survived.

CONCLUSIONS

Conotruncal anomalies can be diagnosed by prenatal echocardiography with a high degree of accuracy. Defining the exact spatial relationship of the great arteries is problematic in some fetuses. The overall prognosis for fetuses with a conotruncal anomaly is poor, with the exception of uncomplicated TOF.

摘要

目的

本研究旨在确定产前超声心动图对圆锥干畸形胎儿的诊断准确性及预后情况。

背景

已有关于心脏病变产前超声心动图诊断准确性的报道,但此前尚无专门针对胎儿圆锥干畸形的报道。

方法

回顾了61例胎儿的病历,这些胎儿均经产前诊断为圆锥干畸形。所涵盖的疾病类型包括法洛四联症(TOF)、右心室双出口(DORV)、大动脉转位(TGA)及永存动脉干(TA)。

结果

胎儿诊断确立时的孕周中位数为24.5周。31%(19/61)的病例选择了终止妊娠。12例未获得产后诊断评估。排除两组联体双胎后,47例中的36例(77%)实现了包括大动脉方位定义在内的准确产前诊断。17例具有DORV解剖结构的胎儿中,有7例产前对大动脉关系的评估有误,其中6例被认为存在肺动脉瓣下室间隔缺损(VSD)。1例被认为表现为TA特征的胎儿存在主动脉闭锁合并VSD及正常大小的左心室。在继续妊娠的42例中,15例伴有严重的心外畸形和/或染色体异常,其中1例因1三体综合征和TA在宫内死亡。另有9例在新生儿期死亡。在27例无染色体或严重心外异常记录的胎儿中,13例(48%)死亡。总体而言,出生后28天以上的存活率为52%(22/42)。相比之下,排除肺动脉瓣缺如综合征的TOF胎儿中,75%(6/8)存活。

结论

圆锥干畸形可通过产前超声心动图进行高度准确的诊断。在一些胎儿中,明确大动脉的确切空间关系存在问题。除单纯性TOF外,圆锥干畸形胎儿的总体预后较差。

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