Accuracy of pulse oximetry screening for detecting critical congenital heart disease in the newborns in rural hospital of Central India.

BACKGROUND

Congenital cardiovascular malformations are the most common category of birth defects and responsible for mortality in the first twelve months of life. Critical congenital heart disease (CCHD) will be present in approximately one quarter of these children, which requires catheter or surgery intervention in the first year of life.

AIM: To determine the accuracy of pulse oximetry for detecting clinically unrecognized CCHD in the newborns.

METHODS

Pulse oximetry was performed on clinically normal newborns within first 4 hours of life. If screening oxygen saturation (SpO2) was below 90%, echocardiography was then performed.

INCLUSION CRITERIA: All newborns who were admitted in postnatal ward & NICU.

EXCLUSION CRITERIA: Out born babies and babies with a prenatal diagnosis of duct dependent circulation.

RESULTS

Pulse-oximetric screening was performed on 2110 clinically normal newborns. Low SpO2 (<90%) was found in eight babies seven of them had CCHD, including three neonates with TGA, two with tricuspid atresia, one with tetralogy of fallot and one with transposition of great vessels. A pulse oximetry cut-off value of below 90% for detecting CCHD showed 100% sensitivity, 99.95% specificity, 87.50% positive predictive value, 100% negative predictive value.

CONCLUSIONS

Pulse oximetry is safe, feasible and noninvasive, can be used as screening tool for detecting CCHD in clinically normal newborn. If SpO2 is below 90% in clinically normal newborns within 4 hours of birth, urgent echocardiography is suggested to rule out CCHD.