학술논문

Contemporary Outcomes in Tetralogy of Fallot With Absent Pulmonary Valve After Fetal Diagnosis
Document Type
article
Source
Journal of the American Heart Association. 10(12)
Subject
Infant Mortality
Pediatric
Lung
Genetics
Clinical Research
Perinatal Period - Conditions Originating in Perinatal Period
Reproductive health and childbirth
Good Health and Well Being
Canada
Echocardiography
Doppler
Color
Fetal Death
Fetal Heart
Humans
Predictive Value of Tests
Prognosis
Pulmonary Valve
Retrospective Studies
Risk Assessment
Risk Factors
Tetralogy of Fallot
Ultrasonography
Prenatal
United States
Ventricular Dysfunction
Left
Ventricular Dysfunction
Right
congenital heart disease
fetal cardiology
fetal echocardiography
prenatal diagnosis
tetralogy of Fallot with absent pulmonary valve
Cardiorespiratory Medicine and Haematology
Language
Abstract
Background Tetralogy of Fallot with absent pulmonary valve is associated with high mortality, but it remains difficult to predict outcomes prenatally. We aimed to identify risk factors for mortality in a large multicenter cohort. Methods and Results Fetal echocardiograms and clinical data from 19 centers over a 10-year period were collected. Primary outcome measures included fetal demise and overall mortality. Of 100 fetuses, pregnancy termination/postnatal nonintervention was elected in 22. Of 78 with intention to treat, 7 (9%) died in utero and 21 (27%) died postnatally. With median follow-up of 32.9 months, no deaths occurred after 13 months. Of 80 fetuses with genetic testing, 46% had chromosomal abnormalities, with 22q11.2 deletion in 35%. On last fetal echocardiogram, at a median of 34.6 weeks, left ventricular dysfunction independently predicted fetal demise (odds ratio [OR], 7.4; 95% CI 1.3, 43.0; P=0.026). Right ventricular dysfunction independently predicted overall mortality in multivariate analysis (OR, 7.9; 95% CI 2.1-30.0; P=0.002). Earlier gestational age at delivery, mediastinal shift, left ventricular/right ventricular dilation, left ventricular dysfunction, tricuspid regurgitation, and Doppler abnormalities were associated with fetal and postnatal mortality, although few tended to progress throughout gestation on serial evaluation. Pulmonary artery diameters did not correlate with outcomes. Conclusions Perinatal mortality in tetralogy of Fallot with absent pulmonary valve remains high, with overall survival of 64% in fetuses with intention to treat. Right ventricular dysfunction independently predicts overall mortality. Left ventricular dysfunction predicts fetal mortality and may influence prenatal management and delivery planning. Mediastinal shift may reflect secondary effects of airway obstruction and abnormal lung development and is associated with increased mortality.