Neonatal cortical hyperostosis secondary to prolonged use of prostaglandin E1 in a patient with pulmonary atresia


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Authors

  • Nazan Neslihan Doğan Clinic of Neonatology, Dr. Sami Ulus Maternity and Children Training and Research Hospital, Ankara
  • Dilek Dilli Clinic of Neonatology, Dr. Sami Ulus Maternity and Children Training and Research Hospital, Ankara
  • Melek Pala Akdoğan Clinic of Radiology, Dr. Sami Ulus Maternity and Children Training and Research Hospital, Ankara
  • Utku Arman Örün Clinic of Pediatric Cardiology, Dr. Sami Ulus Maternity and Children Training and Research Hospital, Ankara
  • Hakan Aydın Clinic of Cardiovasculary Surgery, Dr. Sami Ulus Maternity and Children Training and Research Hospital, Ankara
  • Ayşegül Zencircioğlu Clinic of Neonatology, Dr. Sami Ulus Maternity and Children Training and Research Hospital, Ankara

DOI:

https://doi.org/10.5578/GMJ.27969

Keywords:

Prostaglandin E1, cortical hyperostosis, newborn, cyanotic congenital heart disease

Abstract

Pulmonary atresia is a rare congenital cardiac malformation. The newborns with this anomaly are ductus dependent to maintain a continuous and adequate pulmonary blood fl ow. As spontaneous closure of the ductus is expected after few hours or days after birth, the patency of ductus should be provided by prostaglandin E1 (PGE1) while the patient is awaiting cardiosurgical intervention. PGE1 infusion is usually applied for a short time period. However, in some circumstances, the infusion duration may extend from weeks to months. Long term PGE1 infusions may produce several adverse effects. In this report, we presented a case of newborn with pulmonary atresia who developed cortical hyperostosis secondary to prolonged use of PGE1.

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Published

2016-01-01

How to Cite

Doğan, N. N., Dilli, D., Pala Akdoğan, M., Örün, U. A., Aydın, H., & Zencircioğlu, A. (2016). Neonatal cortical hyperostosis secondary to prolonged use of prostaglandin E1 in a patient with pulmonary atresia. European Journal of Therapeutics, 22(1), 51–53. https://doi.org/10.5578/GMJ.27969

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Section

Case Reports