Sex Differences in Patients Receiving Left Ventricular Assist Devices for End-Stage Heart Failure.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
09 2020
Historique:
received: 27 03 2020
revised: 07 04 2020
accepted: 07 04 2020
pubmed: 13 7 2020
medline: 31 8 2021
entrez: 13 7 2020
Statut: ppublish

Résumé

This study sought to use INTERMACS (Interagency Registry for Mechanically Assisted Circulatory Support) results to evaluate sex differences in the use and clinical outcomes of left ventricular assist devices (LVAD). Despite a similar incidence of heart failure in men and women, prior studies have highlighted potential underuse of LVADs in women, and studies of clinical outcomes have yielded conflicting results. Patients were enrolled from the INTERMACS study who underwent implantation of their first continuous-flow LVAD between 2008 and 2017, and survival analyses stratified by sex were conducted. Among the 18,868 patients, 3,984 (21.1%) were women. At 1 year, women were less likely to undergo heart transplantation than men (17.9% vs. 20.0%, respectively; p = 0.003). After multivariable adjustments, women had a higher risk of death (hazard ratio [HR]: 1.15; 95% confidence interval [CI]: 1.07 to 1.23; p < 0.001) and were more likely to incur post-implantation adverse events, including rehospitalization, bleeding, stroke, and pump thrombosis or device malfunction. Although women younger than 50 years of age had an increased risk of death compared to men of the same age (HR: 1.34; 95% CI: 1.12 to 1.6), men and women 65 years of age and older had a similar risk of death (HR: 1.09; 95% CI: 0.95 to 1.24). This study found that women had a higher risk of mortality and adverse events after LVAD. Only 1 in 5 LVADs were implanted in women, and women were less likely to receive a heart transplant than men. Further investigation is needed to understand the causes of adverse events and potential underuse of advanced treatment options in women.

Sections du résumé

OBJECTIVES
This study sought to use INTERMACS (Interagency Registry for Mechanically Assisted Circulatory Support) results to evaluate sex differences in the use and clinical outcomes of left ventricular assist devices (LVAD).
BACKGROUND
Despite a similar incidence of heart failure in men and women, prior studies have highlighted potential underuse of LVADs in women, and studies of clinical outcomes have yielded conflicting results.
METHODS
Patients were enrolled from the INTERMACS study who underwent implantation of their first continuous-flow LVAD between 2008 and 2017, and survival analyses stratified by sex were conducted.
RESULTS
Among the 18,868 patients, 3,984 (21.1%) were women. At 1 year, women were less likely to undergo heart transplantation than men (17.9% vs. 20.0%, respectively; p = 0.003). After multivariable adjustments, women had a higher risk of death (hazard ratio [HR]: 1.15; 95% confidence interval [CI]: 1.07 to 1.23; p < 0.001) and were more likely to incur post-implantation adverse events, including rehospitalization, bleeding, stroke, and pump thrombosis or device malfunction. Although women younger than 50 years of age had an increased risk of death compared to men of the same age (HR: 1.34; 95% CI: 1.12 to 1.6), men and women 65 years of age and older had a similar risk of death (HR: 1.09; 95% CI: 0.95 to 1.24).
CONCLUSIONS
This study found that women had a higher risk of mortality and adverse events after LVAD. Only 1 in 5 LVADs were implanted in women, and women were less likely to receive a heart transplant than men. Further investigation is needed to understand the causes of adverse events and potential underuse of advanced treatment options in women.

Identifiants

pubmed: 32653446
pii: S2213-1779(20)30270-5
doi: 10.1016/j.jchf.2020.04.015
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

770-779

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Jadry Gruen (J)

Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut.

Cesar Caraballo (C)

Center for Outcomes Research and Evaluation, Yale University School of Medicine, New Haven, Connecticut.

P Elliott Miller (PE)

Yale National Clinician Scholars Program, Yale University School of Medicine, New Haven, Connecticut; Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut.

Megan McCullough (M)

Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut.

Catherine Mezzacappa (C)

Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut.

Neal Ravindra (N)

Department of Biophysics and Biochemistry, Yale University School of Medicine, New Haven, Connecticut.

Clancy W Mullan (CW)

Section of Cardiac Surgery, Yale University School of Medicine, New Haven, Connecticut.

Samuel W Reinhardt (SW)

Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut.

Makoto Mori (M)

Center for Outcomes Research and Evaluation, Yale University School of Medicine, New Haven, Connecticut; Section of Cardiac Surgery, Yale University School of Medicine, New Haven, Connecticut.

Eric Velazquez (E)

Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut.

Arnar Geirsson (A)

Section of Cardiac Surgery, Yale University School of Medicine, New Haven, Connecticut.

Tariq Ahmad (T)

Center for Outcomes Research and Evaluation, Yale University School of Medicine, New Haven, Connecticut; Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut.

Nihar R Desai (NR)

Center for Outcomes Research and Evaluation, Yale University School of Medicine, New Haven, Connecticut; Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut. Electronic address: nihar.desai@yale.edu.

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