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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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Main Authors: 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
Language:Inglês
Published: Nature Portfolio 2024-12-01
Series:Scientific Reports
Subjects:
Pulmonary arterial hypertension (PAH)
Congenital heart disease (CHD)
Eisenmenger
Predominantly systemic-to-pulmonary shunt
Treat-and-repair
Online Access:https://doi.org/10.1038/s41598-024-81834-9
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