Issues of differential diagnosis of the patent foramen ovale and congenital heart disease - secondary atrial septal defect in newborns in the early neonatal period
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Keywords

patent foramen ovale
atrial septal defect
interatrial septum

How to Cite

Gonchar, M., Boichenko, A., & Kondratova , I. (2020). Issues of differential diagnosis of the patent foramen ovale and congenital heart disease - secondary atrial septal defect in newborns in the early neonatal period. Experimental and Clinical Medicine, 77(4), 43-49. Retrieved from https://ecm.knmu.edu.ua/article/view/408

Abstract

The study involved screening of 230 newborns in the early neonatal period, 125 of whom were prematurely born (main group) at gestational age of 26-37 weeks and 105 healthy full-term newborns (control group) in order to improve the criteria for a differential approach to diagnosing the patent foramen ovale (PFO) and congenital heart disease – secondary atrial septal defect. The study showed that gender differences, the presence of the open arterial duct and atrial septal aneurysm had no significant effect on the period of spontaneous closure of the PFO (p>0.05). After the first year of life, the incidence of spontaneous closure of PFO in full-term infants is 68.7%, in pre-term infants – 34.4%. Anatomic closure of PFO in full-term infants occurs in the first year of life (9.5±3.6, p≤0.05 months); in the majority of pre-term infants during the second year of life (14.3±2.6 months). The study showed that clinical and instrumental data (the size of the defect in the oval fossa region, its hemodynamic development, changes in the heart chambers, 2nd degree tricuspid regurgitation), as well as the presence of GG genotype of polymorphism of β1-adrenoreceptor gene in combination with bradycardia and a decrease in the pulsation index in the great vessels of the brain (anterior cerebral and/or medial cerebral arteries) may be additional criteria for differential diagnosis of the patent foramen ovale and atrial septal defect.
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