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    Systolic Blood Pressure, Cardiac Index and Eisenmenger Syndrome are Predictors of Mortality in Pulmonary Arterial Hypertension-associated with Congenital Heart Disease: An Analysis from the COHARD-PH registry by Muflihatul Baroroh Rochmat, Budi Yuli Setianto, Dyah Wulan Anggrahini, Lucia Kris Dinarti, Anggoro Budi Hartopo

    Published 2025-01-01
    “… Background: Pulmonary arterial hypertension (PAH) is a complication of left-to-right intracardiac shunt congenital heart disease (LtR-shunt CHD). There are several known predictors of mortality in PAH patients, however predictors of mortality in LtR-shunt CHD-associated PAH need to be validated. …”
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