Outcomes With Phosphodiesterase-5 Inhibitor Use After Left Ventricular Assist Device: An STS-INTERMACS Analysis.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
04 2022
Historique:
pubmed: 26 3 2022
medline: 22 4 2022
entrez: 25 3 2022
Statut: ppublish

Résumé

Elevated right ventricular afterload following continuous-flow left ventricular assist device (CF-LVAD) may contribute to late right heart failure (LRHF). PDE5i (phosphodiesterase-5 inhibitors) are used to treat pulmonary hypertension and right heart dysfunction after CF-LVAD, but their impact on outcomes is uncertain. We queried Interagency Registry for Mechanically Assisted Circulatory Support from 2012 to 2017 for adults receiving a primary CF-LVAD and surviving ≥30 days from index discharge. Patients receiving early PDE5i (ePDE5i) at 1 month were propensity-matched 1:1 with controls. The primary outcome was the cumulative incidence of LRHF, defined using prevailing Interagency Registry for Mechanically Assisted Circulatory Support criteria; secondary outcomes included all-cause mortality and major bleeding. Among 9627 CF-LVAD recipients analyzed, 2463 (25.6%) received ePDE5i and 1600 were propensity-matched 1:1 with controls. Before implant, ePDE5i patients had more severe RV dysfunction (13.1% versus 9.6%) and higher pulmonary vascular resistance (2.8±2.7 versus 2.2±2.4 WU), both Compared with propensity-matched controls, adult CF-LVAD patients receiving ePDE5i had similar rates of LRHF, mortality, and major bleeding. While intrinsic patient risk factors likely account for more adverse outcomes with ePDE5i in the unmatched cohort, there is no obvious benefit of ePDE5i in the LVAD population.

Sections du résumé

BACKGROUND
Elevated right ventricular afterload following continuous-flow left ventricular assist device (CF-LVAD) may contribute to late right heart failure (LRHF). PDE5i (phosphodiesterase-5 inhibitors) are used to treat pulmonary hypertension and right heart dysfunction after CF-LVAD, but their impact on outcomes is uncertain.
METHODS
We queried Interagency Registry for Mechanically Assisted Circulatory Support from 2012 to 2017 for adults receiving a primary CF-LVAD and surviving ≥30 days from index discharge. Patients receiving early PDE5i (ePDE5i) at 1 month were propensity-matched 1:1 with controls. The primary outcome was the cumulative incidence of LRHF, defined using prevailing Interagency Registry for Mechanically Assisted Circulatory Support criteria; secondary outcomes included all-cause mortality and major bleeding.
RESULTS
Among 9627 CF-LVAD recipients analyzed, 2463 (25.6%) received ePDE5i and 1600 were propensity-matched 1:1 with controls. Before implant, ePDE5i patients had more severe RV dysfunction (13.1% versus 9.6%) and higher pulmonary vascular resistance (2.8±2.7 versus 2.2±2.4 WU), both
CONCLUSIONS
Compared with propensity-matched controls, adult CF-LVAD patients receiving ePDE5i had similar rates of LRHF, mortality, and major bleeding. While intrinsic patient risk factors likely account for more adverse outcomes with ePDE5i in the unmatched cohort, there is no obvious benefit of ePDE5i in the LVAD population.

Identifiants

pubmed: 35332780
doi: 10.1161/CIRCHEARTFAILURE.121.008613
pmc: PMC9205418
mid: NIHMS1776699
doi:

Substances chimiques

Phosphodiesterase 5 Inhibitors 0
Cyclic Nucleotide Phosphodiesterases, Type 5 EC 3.1.4.35

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e008613

Subventions

Organisme : NHLBI NIH HHS
ID : F32 HL149251
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

E Wilson Grandin (EW)

Cardiovascular Institute, Beth Israel Deaconess Medical Center, Boston MA (E.W.G., J.I.N.).
Smith Center for Outcomes Research in Cardiology, Beth Israel Deaconess Medical Center, Boston, MA (E.W.G., K.K.).

Gaurav Gulati (G)

Cardiovascular Center, Tufts Medical Center, Boston, MA (G.G., M.S.K.).

Jose I Nunez (JI)

Cardiovascular Institute, Beth Israel Deaconess Medical Center, Boston MA (E.W.G., J.I.N.).

Kevin Kennedy (K)

Smith Center for Outcomes Research in Cardiology, Beth Israel Deaconess Medical Center, Boston, MA (E.W.G., K.K.).

J Eduardo Rame (JE)

Division of Cardiology, Jefferson Heart Institute, Philadelphia, PA (J.E.R.).

Pavan Atluri (P)

Division of Cardiothoracic Surgery, Hospital of the University of Pennsylvania, Philadelphia (P.A.).

Francis D Pagani (FD)

Division of Cardiothoracic Surgery, University of Michigan School of Medicine, Ann Arbor (F.D.P.).

James K Kirklin (JK)

Division of Cardiothoracic Surgery, University of Alabama Birmingham School of Medicine (J.K.K.).

Robert L Kormos (RL)

Division of Cardiothoracic Surgery, University of Pittsburgh, PA (R.L.K.).
Abbott Laboratories, Austin, TX (R.L.K.).

Jeffrey Teuteberg (J)

Division of Cardiovascular Medicine, Stanford University Medical Center, Palo Alto, CA (J.T.).

Michael S Kiernan (MS)

Cardiovascular Center, Tufts Medical Center, Boston, MA (G.G., M.S.K.).

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