Pulmonary arterial hypertension after systemic‑to‑pulmonary shunt correction (RCD code: II-1A.4d)

Journal Title: Journal of Rare Cardiovascular Diseases - Year 2013, Vol 1, Issue 3

Abstract

Pulmonary arterial hypertension develops in a significant number of patients with congenital heart diseases. Congenital heart diseases predispose to pulmonary vascular remodeling as a result of increased pulmonary blood flow and increased pulmonary pressure. Pulmonary arterial hypertension associated with congenital heart diseases is a major determinant of functional capacity and survival in this group of patients. JRCD 2013; 1 (3): 32–35

Authors and Affiliations

Magdalena Kaznica-Wiatr, Grzegorz Kopeć, Piotr Podolec

Keywords

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  • EP ID EP245390
  • DOI 10.20418/jrcd.vol1no3.91
  • Views 102
  • Downloads 0

How To Cite

Magdalena Kaznica-Wiatr, Grzegorz Kopeć, Piotr Podolec (2013). Pulmonary arterial hypertension after systemic‑to‑pulmonary shunt correction (RCD code: II-1A.4d). Journal of Rare Cardiovascular Diseases, 1(3), 118-121. https://europub.co.uk./articles/-A-245390