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Survival comparison in adults with congenital systemic to pulmonary shunt and borderline elevated pulmonary vascular resistance versus Eisenmenger syndrome

Abstract Pulmonary arterial hypertension (PAH) associated with congenital heart disease (PAH-CHD) is a consequence of unrepaired large systemic-to-pulmonary shunts. The long-term data of adult patients who have PAH-CHD with elevated pulmonary vascular resistance (PVR) are limited. We aimed to invest...

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Autors principals: Jantaras Sengsim, Chodchanok Vijarnsorn, Prakul Chanthong, Paweena Chungsomprasong, Supaluck Kanjanauthai, Ploy Thammasate, Thita Pacharapakornpong, Nalin Chaiwangyen, Densiri Bositthipichet, Jarupim Soongswang, Teerapong Tocharoenchok, Ekarat Nitiyarom, Kriangkrai Tantiwongkosri, Thaworn Subtaweesin, Kritvikrom Durongpisitkul
Format: Artigo
Idioma:Inglês
Publicat: Nature Portfolio 2024-12-01
Col·lecció:Scientific Reports
Matèries:
Pulmonary arterial hypertension (PAH)
Congenital heart disease (CHD)
Eisenmenger
Predominantly systemic-to-pulmonary shunt
Treat-and-repair
Accés en línia:https://doi.org/10.1038/s41598-024-81834-9
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