胎儿DORV:如何在产前心脏病中心咨询未来的父母?回顾性分析39例病例

Prenatal Cardiology Pub Date : 2014-09-01 DOI:10.12847/09142
M. Soroka, M. Słodki, H. Moczulska, M. Respondek-Liberska
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引用次数: 0

摘要

摘要:双出口右心室是指大血管全部或大部分从形态上的右心室上方离开的一种缺损。我们对DORV缺陷提出了新的产前心脏缺陷分类,将DORV缺陷分为孤立的心外缺陷和共存的心外缺陷,便于对胎儿和新生儿进行会诊和预测预后。孤立的胎儿DORV被归类为严重的选择性缺陷(1月龄时预期的心脏干预或手术),无论心内异常类型如何,新生儿预后相对较好(在我们的一系列病例中,存活率为100%)。同时存在心外缺陷(ECM)的胎儿DORV,无论异常类型如何,预后都很差(在我们的研究组中死亡率为100%)。
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DORV in fetuses: how to consult future parents at a prenatal cardiology center? Retrospective analysis of 39 cases
Abstract DORV [double outlet right ventricle] is defined as a defect in which the great vessels leave entirely or mostly from above the morphologically right ventricle. The proposed by us new prenatal classification of heart defects for the DORV defect including the division into isolated and coexisting with extracardiac defect, facilitates consultation and predicting prognosis for the fetus and newborn. Isolated DORV in fetuses is classified as a severe elective defect (expected cardiac intervention or surgery at 1 month of age) with a relatively good prognosis for newborns, regardless of the type of intracardiac anomalies (in our series of cases 100% survival). DORV in the fetus with coexisting extracardiac defects (ECM) regardless of type of anomaly had poor prognosis (in our study group 100% demise rate).
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