Key result
A male neonate with idiopathic prenatal closure of the ductus arteriosus causing fetal hydrops was successfully resuscitated and discharged with normal development on follow-up.
Why the study?
Spontaneous premature closure of the human fetal ductus arteriosus is uncommon and frequently leads to significant morbidity and mortality.
Case Report (n=1)
No
Idiopathic prenatal closure of the ductus arteriosus can cause severe fetal hydrops and requires prompt postnatal intensive care and echocardiographic evaluation.
Answers are grounded in this paper and cite their sources.
Successful resuscitation feasible in rare idiopathic prenatal ductus closure with hydrops; leaves open incidence, etiology, and prevention strategies.
Spontaneous premature closure of the human fetal ductus arteriosus is an uncommon event that often results in significant morbidity and mortality. We present a case of a neonate with prenatal previously not detected intrauterine closure of the ductus arteriosus in a 21-year-old ,G3P1A2L1 mother with type 2 consanguinity at 39 weeks of gestation, with previous scans showing placenta previa grade 1 at 21weeks and Doppler study showing pericardial effusion at 36weeks.Caesarean section was performed in view of absent progression of labour. A male newborn weighing 4100gm, required bag and mask and intubation. With an excellent neonatal outcome. Finally we suggest that fetal echo in third trimester & maternal education programs to avoid self-medication and provide training for good diet is necessary.
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Gavade et al. (2020) conducted a case report in Prenatal closure of the ductus arteriosus causing fetal hydrops (n=1). Enoxaparin (maternal exposure) was evaluated on Neonatal survival and clinical recovery. A male neonate with idiopathic prenatal closure of the ductus arteriosus causing fetal hydrops was successfully resuscitated and discharged with normal development on follow-up.
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