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Tailored strategy to match anatomy and physiology with intervention can improve outcomes of symptomatic neonates with Ebstein anomaly.
Pizarro, Christian; Bhat, Majeed A; Davis, Deborah A; Duncan, Daniel; Pelletier, Glenn J; Baffa, Gina.
Afiliação
  • Pizarro C; Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.
  • Bhat MA; Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.
  • Davis DA; Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.
  • Duncan D; Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.
  • Pelletier GJ; Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.
  • Baffa G; Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.
JTCVS Open ; 12: 344-354, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36590729
ABSTRACT

Objective:

Neonatal presentation of Ebstein anomaly (EA) represents the most severe form of this condition. Despite significant advances, operative mortality remains high and management decisions represent a formidable challenge. We used a strategy aimed to match anatomy and physiology with type and time of intervention to increase survival.

Methods:

We performed a review of all patients with fetal or neonatal diagnosis of EA managed at a single center between 2007 and 2020.

Results:

Among 18 patients with EA, 8 underwent neonatal intervention. The most common indication included cyanosis and heart failure (8/8), end organ dysfunction (6/8), and maldistribution of cardiac output (6/8). Only 2/8 had antegrade pulmonary blood flow. Associated conditions included pulmonary regurgitation in 4/8, atrial tachyarrhythmia in 4, and a ventricular septal defect in 3. Three patients underwent initial stabilization with main pulmonary artery occlusion including bilateral pulmonary artery banding in 2. Five patients underwent biventricular repair with conversion to right ventricle exclusion in 2 cases. Three others underwent the Starnes procedure as initially planned. The median age at surgery was 10 days (range, 1-30) and median weight 2.6 kg (range, 1.9-4.0). The median duration of mechanical ventilation and intensive care unit stay were 9 days (range, 5-34) and 30 days (range, 15-100), respectively. Operative mortality was 1/8. At a median follow-up of 130 months (range, 5-146), there were no late deaths, and all survivors remain in functional class I and free of valvular reintervention.

Conclusions:

Symptomatic neonates with EA can be effectively managed with good outcomes. Preoperative stabilization and choice of management pathway on the basis of anatomy and physiology can help reduce morbidity and mortality.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: JTCVS Open Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: JTCVS Open Ano de publicação: 2022 Tipo de documento: Article