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Acute unloading effects of sildenafil enhance right ventricular–pulmonary artery coupling in heart failure

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F21%3A00080787" target="_blank" >RIV/00023001:_____/21:00080787 - isvavai.cz</a>

  • Result on the web

    <a href="https://reader.elsevier.com/reader/sd/pii/S107191642031513X?token=6B13BEADB14B8435CC7DD2A704228AFE66A27DE15352C8C110E71ADBEDBACE0AAD77C870FC8FC64CD4DC0F46F44096AA" target="_blank" >https://reader.elsevier.com/reader/sd/pii/S107191642031513X?token=6B13BEADB14B8435CC7DD2A704228AFE66A27DE15352C8C110E71ADBEDBACE0AAD77C870FC8FC64CD4DC0F46F44096AA</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cardfail.2020.11.007" target="_blank" >10.1016/j.cardfail.2020.11.007</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Acute unloading effects of sildenafil enhance right ventricular–pulmonary artery coupling in heart failure

  • Original language description

    Background: Phosphodiesterase-5A inhibitors (PDE5i) are sometimes used in patients with advanced heart failure with reduced ejection fraction before heart transplant or left ventricular assist device implantation to decrease right ventricular (RV) afterload and mitigate the risk of right heart failure. Conflicting evidence exists regarding the impact of these drugs on RV contractility. The aim of this study was to explore the acute effects of PDE5i on ventricular–vascular coupling and load-independent RV contractility. Methods: Twenty-two patients underwent right heart catheterization and gated equilibrium blood pool single photon emission computed tomography, before and after 20 mg intravenous sildenafil. Single photon emission computed tomography and right heart catheterization-derived data were used to calculate RV loading and contractility. Results: PDE5i induced a decrease in the right atrial pressure (–43%), pulmonary artery (PA) mean pressure (–26%), and PA wedge pressure (PAWP; –23%), with favorable reductions in pulmonary vascular resistance (–41%) and PA elastance (–40%), and increased cardiac output (+13%) (all P &lt; 0.01). The RV ejection fraction increased with sildenafil (+20%), with no change of RV contractility (P = 0.74), indicating that the improvement in the RV ejection fraction was related to enhanced RV–PA coupling (r = 0.59, P = 0.004) by a decrease in the ventricular load. RV diastolic compliance increased with sildenafil. The decrease in the PAWP correlated with RV end-diastolic volume decrease; no relationship was observed with the change in LV transmural pressure, suggesting decreased pericardial constraint. Conclusions: Acute PDE5i administration has profound RV afterload-reducing effects, improves the RVEF, decreases RV volumes, and decreases the PAWP, predominantly through relief of pericardial constraint, without effects on RV chamber contractility. These findings support further study of PDE5i in protection of RV function in advanced heart failure with reduced ejection fraction who are at risk of RV failure. © 2020 Elsevier Inc.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30201 - Cardiac and Cardiovascular systems

Result continuities

  • Project

    <a href="/en/project/NV17-28784A" target="_blank" >NV17-28784A: Mechanisms of right ventricular dysfunction in chronic heart failure</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of cardiac failure

  • ISSN

    1071-9164

  • e-ISSN

  • Volume of the periodical

    27

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    224-232

  • UT code for WoS article

    000617764200016

  • EID of the result in the Scopus database

    2-s2.0-85097234520