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Hemodynamic and prognostic impact of the diastolic pulmonary arterial pressure in children with pulmonary arterial hypertension—a registry-based analysis
Author(s) -
Christian Apitz,
Rolf M.F. Berger,
D. Dunbar Ivy,
Tilman Humpl,
Damien Bonnet,
Maurice Beghetti,
Dietmar Schranz,
Heiner Latus
Publication year - 2021
Publication title -
cardiovascular diagnosis and therapy
Language(s) - English
Resource type - Journals
eISSN - 2223-3660
pISSN - 2223-3652
DOI - 10.21037/cdt-20-934
Subject(s) - medicine , pulmonary hypertension , cardiology , vascular resistance , hemodynamics , transpulmonary pressure , lung transplantation , diastole , pulmonary artery , transplantation , blood pressure , lung , lung volumes
Diastolic pulmonary arterial pressure (dPAP) is regarded to be less sensitive to flow metrics as compared to mean PAP (mPAP), and was therefore proposed for the assessment of a precapillary component in patients with postcapillary pulmonary hypertension (PH). To analyze the diagnostic and prognostic impact of dPAP in patients with pure precapillary PH, we purposed to compare the correlation between dPAP and mPAP, as well as hemodynamically-derived calculations [ratio of PAP to systemic arterial pressure (PAP/SAP), pulmonary vascular resistance index (PVRI), transpulmonary gradient (TPG)], using both dPAP and mPAP, at rest and during acute vasoreactivity testing (AVT) in children with idiopathic or heritable pulmonary arterial hypertension (IPAH/HPAH). Furthermore, we aimed to assess the association of these metrics (at baseline and changes after AVT) with transplant-free survival.

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