What question did this study set out to answer?

April 17, 2026Open Access

High rates of congenital airway anomalies in neonates with single ventricle congenital heart disease

Puntos clave

The aim is to assess the prevalence of congenital airway anomalies in neonates with single ventricle congenital heart disease.
Analyzed neonatal admissions from a national administrative database using ICD-10 codes.
Focused on SV CHD cases with and without congenital airway anomalies.
Excluded admissions with genetic syndromes to minimize confounding factors.
10.4% of neonates with SV CHD have congenital airway anomalies.
Significant odds ratio of 28.9 indicates higher prevalence compared to those without CHD.
Neonates with both SV CHD and CAA had longer hospital stays, more complications, and higher mortality.

Resumen

Neonates with single ventricle congenital heart disease (SV CHD) may have noncardiac comorbidities, including congenital airway anomalies (CAA). Using a national administrative database, we analyzed neonatal admissions with ICD-10 codes for SV CHD with and without CAA from October 2020 to December 2024, excluding admissions with genetic syndromes to reduce confounding by the potential contribution of syndromes to CAA. Among 5144 neonatal admissions with SV CHD, 535 (10.4%) had CAA, compared to 23,837 (0.4%) of 5,942,621 neonatal admissions without CHD (odds ratio OR 95% confidence interval: 28.9 26.4, 31.7, P < 0.001). Neonates with SV CHD and CAA had longer lengths of stay, more complications, inhospital mortality, and higher hospital costs compared to those without CAA. This study highlights the markedly higher prevalence of CAA in neonates with SV CHD and the negative impact on hospital outcomes.

Leer artículo completoexternamente

Me gusta

Guardar

Ver artículo completo