Pulmonary Artery Measurements as Postnatal Prognostic Tool in Right Congenital Diaphragmatic Hernia

Space: StayCurrentMD Author: Sung Hyeon Park, Ji Yoo Kim, Keon Hee Seol, Joo Hyung Roh, Ha Na Lee, Soo Hyun Kim, Jiyoon Jeong, Jung-Man Namgoong, Byong Sop Lee, Euiseok Jung Published:

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Sung Hyeon Park, Ji Yoo Kim, Keon Hee Seol, Joo Hyung Roh, Ha Na Lee, Soo Hyun Kim, Jiyoon Jeong, Jung-Man Namgoong, Byong Sop Lee, Euiseok Jung

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Right-sided congenital diaphragmatic hernia (RCDH) is a rare and often fatal congenital anomaly, primarily attributed to lung hypoplasia, which is associated with small branch pulmonary artery (PA). This study investigated whether postnatal PA measurements obtained through echocardiography are associated with mortality or the extracorporeal membrane oxygenation (ECMO) requirement in neonates with RCDH.

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