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Effects of Phosphodiesterase Type 5 Inhibition on Systemic and Pulmonary Hemodynamics and Ventricular Function in Patients With Severe Symptomatic Aortic Stenosis
Author(s) -
Brian R. Lindman,
Alan Zajarías,
José A. Madrazo,
Jay Shah,
Brian F. Gage,
Eric Novak,
Stephanie N. Johnson,
Murali M. Chakinala,
Tara A. Hohn,
Sultan Ayesh Mohammed Saghir,
Douglas L. Mann
Publication year - 2012
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.111.081125
Subject(s) - medicine , sildenafil , cardiology , hemodynamics , cgmp specific phosphodiesterase type 5 , pulmonary wedge pressure , vascular resistance , stenosis , pressure overload , heart failure , pulmonary hypertension , pulmonary artery , phosphodiesterase inhibitor , cardiac hypertrophy
Pressure overload resulting from aortic stenosis causes maladaptive ventricular and vascular remodeling that can lead to pulmonary hypertension, heart failure symptoms, and adverse outcomes. Retarding or reversing this maladaptive remodeling and its unfavorable hemodynamic consequences has the potential to improve morbidity and mortality. Preclinical models of pressure overload have shown that phosphodiesterase type 5 inhibition is beneficial; however, the use of phosphodiesterase type 5 inhibitors in patients with aortic stenosis is controversial because of concerns about vasodilation and hypotension.

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