Navigating the spectrum of double‐outlet right ventricle presentations: Outcomes from a contemporary cohort based on subtypes

Author:

Öcal Aydın1ORCID,Demirci Oya1ORCID,Kahramanoğlu Özge1ORCID,Ayhan Işıl1ORCID,Erol Nurdan2ORCID,Yücel İlker Kemal3ORCID

Affiliation:

1. Department of Perinatology Zeynep Kamil Women and Children's Diseases Training and Research Hospital University of Health Sciences Istanbul Turkey

2. Department of Pediatric Cardiology Zeynep Kamil Women and Children's Diseases Training and Research Hospital University of Health Sciences Istanbul Turkey

3. Department of Pediatric Cardiology Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training & Research Hospital University of Health Sciences Istanbul Turkey

Abstract

AbstractPurposeOur aim in this study was to investigate the prenatal and postnatal prognosis of double outlet right ventricle (DORV) cases diagnosed prenatally by analyzing the outcomes based on the subtype.MethodsThis study is a retrospective chart review. Cases diagnosed with fetal DORV by prenatal ultrasound in the maternal–fetal medicine department of our hospital between 2014 and 2022 were included. Data on maternal characteristics, fetal echocardiographic features (type of DORV), pregnancy and neonatal outcomes (termination of pregnancy [TOP], intrauterine fetal death [IUD], neonatal death [NND], death in infancy (IND), survival) were collected and analyzed.ResultsNinety‐nine cases of prenatally diagnosed cases of DORV were included. The prenatal diagnosis was right in 97% of the liveborn fetuses. The cases were classified into subtypes, including transposition of great arteries (TGA), Fallot, ventricular septal defect (VSD), remote, and heterotaxy types. The cohort consisted of 32.3% TGA type, 19.1% fallot type, 11.1% VSD type, 2% remote type, and 35.3% heterotaxy type of DORV. An additional cardiac anomaly was observed in 87% and an extra‐cardiac anomaly was observed in 54% of the cases. When we excluded the cases with heterotaxy type but without any chromosomal abnormality, additional genetic abnormalities were detected in 42% of the remaining cases. Outcome of pregnancy was livebirth in 68/99 (68.7%), IUFD in 5/99 (5.1%), and TOP in 26/99 (26.3%). Postnatal cardiac surgical repair was performed in 48 cases. Survival among livebirths was 39/68 (57.3%). Twenty‐nine neonates or infants who had additional cardiac anomalies and/or genetic abnormalities died before any surgical intervention. The postoperative survival rate was 39/48 (81.2%).ConclusionThe prognosis in DORV depends on the anatomical subtype, the presence, and severity of associated anomalies. Survival increases in isolated cases without any additional structural or genetic anomalies.

Publisher

Wiley

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