Abstract
I. Description
A. Persistent pulmonary hypertension of the newborn (PPHN) is a condition in which pulmonary vascular resistance (PVR) is elevated, usually from a failure of its normal postbirth decline. This leads to a variable degree of right-to-left shunting through persistent fetal channels, the foramen ovale and ductus arteriosus, and resultant hypoxemia. A similar clinical picture can arise from decreased systemic vascular resistance (SVR), or any condition where the PVR:SVR ratio is >1. Originally called persistent fetal circulation (PFC), it was a diagnosis seen in term babies with “clear” lung fields on radiography, profound cyanosis, and a structurally normal heart. Secondary PPHN also occurs in babies with primary pulmonary parenchymal disease or with left ventricular dysfunction.
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Stepanovich, G., Schumacher, R.E., Donn, S.M. (2022). Persistent Pulmonary Hypertension of the Newborn. In: Donn, S.M., Mammel, M.C., van Kaam, A.H. (eds) Manual of Neonatal Respiratory Care. Springer, Cham. https://doi.org/10.1007/978-3-030-93997-7_71
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DOI: https://doi.org/10.1007/978-3-030-93997-7_71
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