Key result
A normal level II ultrasound did not miss any critical congenital heart disease in fetuses with a sibling with the condition, yielding a negative predictive value of 100%.
Why the study?
Fetal echocardiograms are routinely recommended when a sibling has congenital heart disease even after a normal level II ultrasound, but whether critical congenital heart disease is ever missed by ultrasound in this population remains unclear.
Does screening fetal echocardiogram detect critical congenital heart disease in fetuses with a sibling with CHD who already had a normal level II ultrasound?
Observational (n=113)
No
Does screening fetal echocardiogram detect critical congenital heart disease in fetuses with a sibling with CHD who already had a normal level II ultrasound?
In fetuses with a sibling with congenital heart disease and a normal level II ultrasound, routine screening fetal echocardiograms did not identify any additional cases of critical CHD, suggesting limited added clinical value.
May support omitting routine fetal echocardiography after normal level II ultrasound in fetuses with affected siblings; leaves open confirmation in larger cohorts.
INTRODUCTION: In pregnancies when congenital heart disease (CHD) is present in siblings, fetal echocardiograms (F-echo) are recommended, regardless if there was a prior level II ultrasound (LII-US) that was normal. The goal of this study was to evaluate if any diagnosis of a critical congenital heart disease (CHD) was missed in a fetus who had a sibling with CHD, when a normal LII-US was documented. METHODS: Retrospective chart review of all F-echo where the indication was sibling with CHD between January 1, 2019 and December 31, 2023 was performed. Fetuses were included if they had a LII-US that was read as normal and had a F-echo. Critical CHD was defined as CHD requiring catheterization or surgical intervention < 1 month of age. RESULTS: A total of 187 F-echo on fetuses who had a sibling with CHD were evaluated, of which 113 met inclusion criteria. LII-US was performed at 21.1 ± 3.3 weeks gestational age and F-echo was performed at 25.4 ± 3.1 weeks gestational age. No patient with a normal LII-US had a diagnosis of a critical CHD by F-echo (negative predictive value = 100%). Six patients that had a negative LII-US were diagnosed with non-critical CHD or cardiac issues postnatally (negative predictive value = 94.7%). F-echo correctly diagnosed two of the six missed LII-US CHD. CONCLUSION: Critical CHD was not missed with a normal LII-US in this at-risk population. F-echo also missed the majority of CHD when a LII-US was read as normal. The cost/benefit of screening F-echo in fetuses with siblings with CHD should be evaluated if a normal LII-US has been performed. Larger studies are needed to determine if these findings remain consistent.
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Taylor et al. (2025) conducted an observational in Fetuses with siblings with congenital heart disease (n=113). Fetal echocardiogram after normal level II ultrasound was evaluated on Missed diagnosis of critical congenital heart disease (negative predictive value of normal level II ultrasound) (NPV 100%). A normal level II ultrasound did not miss any critical congenital heart disease in fetuses with a sibling with the condition, yielding a negative predictive value of 100%.
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