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ABSTRACT: Background
Elevated mean pulmonary artery pressure (mPAP) is common in patients with hypertrophic cardiomyopathy (HCM) and heart failure symptoms. However, dynamic left ventricular (LV) outflow tract obstruction may confound interpretation of pulmonary hypertension (PH) pathophysiologic features in HCM when relying on resting invasive hemodynamic data alone.Research question
Do structural changes to the lung vasculature clarify PH pathophysiologic features in patients with HCM with progressive heart failure?Study design and methods
Clinical data and ultrarare lung autopsy specimens were acquired retrospectively from the National Institutes of Health (1975-1992). Patients were included based on the availability of lung tissue and recorded mPAP. Discarded tissue from
SUBMITTER: Maron BA
PROVIDER: S-EPMC9993337 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature