REVISTA DE EDUCATIE MEDICALA CONTINUA DEDICATA GINECOLOGILOR,
OBSTETRICENILOR, MOASELOR SI ASISTENTILOR MEDICALI DIN ROMANIA

<- Home <- Arhive <- Anul 5, Nr. 16, June 2017



RevistaGinecologia5(16)56-64(2017)
© VERSA PULS MEDIA, S.R.L.


Aortic coarctation - difficulties of fetal diagnosis. Case report and literature review

S. Vlădăreanu, I. Petrescu, A. Dumitrescu, G. Iordache, M. Mitran


Rezumat: The aortic coarctation (CoA) is the most frequently omitted ductal-dependent cardiac deffect on neonatal screening and also one of the most difficult diagnosis to establish before birth. It is estimated that 60-80% from the newborns with isolated CoA are discharged at home from neonatal departament as healthy babies, later developing hemodynamic complications, that appear suddenly or gradually as a consequence of closing the arterial ductus. So, it is absolutely necessary to make the cardiac screening for every newborn before discharging. It consists of preand postductal pulsoximetry and measuring the blood pressure to all four limbs. Also, it is necessary to confirm this diagnosis by the fetal cardiologist in all cases of CoA suspected and the pregnant women to be oriented for delivery in a specialized centre in cardiac intensive neonatal care. At fetal ultrasound, the suspicion of CoA is increased by ventricular and large vessels disproportion signs and in 4-chambers view and/or 3-vessels and trachea especially in the first and second trimesters of pregnancy. However, the prenatal screening registers a high rate of fals-positive and false-negative results. The prenatal diagnosis improves and reduces the morbidity by allowing to plan the delivery in a tertiary center and to establish the treatment with PGE to prevent the constriction of arterial duct. We present the case of a term newborn (38 weeks) born by caesarian section performed in the Obstetrics and Ginecology Clinic of the “Elias” Hospital, antenatal suspicioned with CoA, following two ultrasounds performed at 34 and 35 weeks of gestation. The newborn is treated with PGE medication from the first hour of life. After two days of life, the pediatric cardiologist excluded this diagnosis by echocardiography in “M.S.Curie” Hospital. The treatment with PGE was slowly interrupted and the neonatal evolution was favorable.
Cuvinte cheie: aortic coarctation, newborn, permeable arterial duct, echocardiography, aortic arch, prostaglandine.

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