Right ventricular outflow tract anomalies: Neonatal interventions and outcomes

被引：4
|
作者：
Arunamata, Alisa [1 ]
Goldstein, Bryan H. [2 ]
机构：
[1] Stanford Univ, Sch Med, Dept Pediat, Div Pediat Cardiol, Stanford, CA 94305 USA
[2] Univ Pittsburgh, Sch Med, Dept Pediat, Heart Inst,UPMC Childrens Hosp Pittsburgh, Pittsburgh, PA 15261 USA
来源：
SEMINARS IN PERINATOLOGY | 2022年 / 46卷 / 04期
关键词：
Congenital heart disease; Right ventricular outflow tract; Tetralogy of Fallot; Pulmonary atresia; Pulmonary stenosis; Ebstein anomaly; Cardiac catheterization; Congenital heart surgery; PULMONARY VALVE-REPLACEMENT; CONGENITAL HEART-DEFECTS; SUDDEN CARDIAC DEATH; REPAIRED TETRALOGY; NATURAL-HISTORY; BALLOON VALVULOPLASTY; TRICUSPID-VALVE; ECHOCARDIOGRAPHIC PREDICTORS; SCIENTIFIC STATEMENT; MAGNETIC-RESONANCE;
D O I：
10.1016/j.semperi.2022.151583
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
Right ventricular outflow tract (RVOT) anomalies comprise a wide spectrum of congenital heart disease, typically characterized by obstruction to flow from the right ventricle to pulmonary arteries. This review highlights important considerations surrounding management strategy as well as clinical outcomes for the neonate with RVOT anomaly, including: pulmonary atresia with intact ventricular septum, congenital pulmonary valve stenosis, tetralogy of Fallot, and Ebstein anomaly with anatomic or physiologic RVOT obstruction.(c) 2022 Elsevier Inc. All rights reserved.
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页数：14
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