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Critical Congenital Heart Disease Detection in the Screening Era: Do Not Neglect the Examination!
Deepika Sankaran1, Heather Siefkes2, Frank F Ing3
1Division of Neonatology, Department of Pediatrics, University of California, Davis, Sacramento, California.
Insights
Critical congenital heart disease screening using pulse oximetry can miss pulmonary atresia. This case highlights the importance of thorough newborn physical exams alongside screening for early diagnosis.
Area of Science:
- Neonatal Cardiology
- Pediatric Critical Care
- Congenital Heart Disease Screening
Background:
- Pulse oximetry oxygen saturation (SpO2)-based screening effectively detects cyanotic heart lesions in newborns.
- Critical congenital heart disease (CCHD) screening aims to identify serious heart conditions before discharge.
Observation:
- A full-term infant with normal perfusion passed CCHD screening (preductal SpO2 99%, postductal SpO2 97%).
- A loud systolic murmur detected before discharge led to a diagnosis of pulmonary atresia with ventricular septal defect (PA-VSD) via echocardiogram.
Findings:
- This case represents the first documented instance of pulmonary atresia missed by CCHD screening.
- The infant remained hemodynamically stable and asymptomatic without respiratory distress or desaturation on pulse oximetry initially.
Implications:
- Thorough and serial clinical examinations are crucial for diagnosing critical congenital heart diseases like PA-VSD.
- Pulse oximetry screening is a valuable tool but should complement, not replace, comprehensive physical assessments in newborns.
Abstract:
Pulse oximetry oxygen saturation (SpO 2 )-based critical congenital heart disease (CCHD) screening is effective in detection of cyanotic heart lesions. We report a full-term male infant with normal perfusion who had passed the CCHD screening at approximately 24 hours after birth with preductal SpO 2 of 99% and postductal SpO 2 of 97%. Detection of a loud systolic cardiac murmur before discharge led to the diagnosis of pulmonary atresia (PA) with ventricular septal defect (PA-VSD) by echocardiogram. The infant was transferred to a tertiary care center after initiation of prostaglandin E1 (PGE1) therapy. Throughout the initial course, he was breathing comfortably without respiratory distress or desaturations on pulse oximetry. We believe that this is the first documented report of PA missed by CCHD screening. Thorough and serial clinical examinations of the newborn infant proved vital in the timely diagnosis of this critical disease. We review the hemodynamics and the recent literature evaluating utility of CCHD screening in the diagnosis of PA-VSD. Pulse oximetry-based CCHD screening should be considered a tool to enhance CCHD detection with an emphasis on detailed serial physical examinations in newborn infants.
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