Metabolic Dysfunction in Continuous-Flow Left Ventricular Assist Devices Patients and Outcomes.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
19 11 2019
Historique:
entrez: 14 11 2019
pubmed: 14 11 2019
medline: 15 12 2020
Statut: ppublish

Résumé

Background Metabolic impairment is common in heart failure patients. Continuous-flow left ventricular assist devices (CF-LVADs) improve hemodynamics and outcomes in patients with advanced heart failure; however, the effect of CF-LVADs on metabolic status is unknown. This study aims to evaluate the changes in metabolic status following CF-LVAD implantation and measure the correlation of metabolic status with outcomes. Methods and Results Prospective data on CF-LVAD patients were obtained. Metabolic evaluation, including hemoglobin A1C, free and total testosterone, thyroid-stimulating hormone (TSH), and free T4, was obtained before and at multiple time points following implantation. Patients with nonelevated thyroid-stimulating hormone and normal hemoglobin A1C and testosterone levels were defined as having normal metabolic status. Baseline characteristics, hemodynamics, and outcomes were collected. One hundred six patients were studied, of which 56 had paired data at baseline and 1- to 3-month follow-up. Before implantation, 75% of patients had insulin resistance, 86% of men and 39% of women had low free testosterone, and 44% of patients had abnormal thyroid function. There was a significant improvement in hemoglobin A1C, free testosterone, and thyroid-stimulating hormone following implantation (

Identifiants

pubmed: 31718441
doi: 10.1161/JAHA.119.013278
pmc: PMC6915293
doi:

Substances chimiques

Glycated Hemoglobin A 0
hemoglobin A1c protein, human 0
Testosterone 3XMK78S47O
Thyrotropin 9002-71-5
Thyroxine Q51BO43MG4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e013278

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL007381
Pays : United States

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Auteurs

Ann B Nguyen (AB)

Section of Cardiology Department of Medicine University of Chicago IL.

Teruhiko Imamura (T)

Section of Cardiology Department of Medicine University of Chicago IL.

Stephanie Besser (S)

Section of Cardiology Department of Medicine University of Chicago IL.

Daniel Rodgers (D)

Section of Cardiology Department of Medicine University of Chicago IL.

Ben Chung (B)

Section of Cardiology Department of Medicine University of Chicago IL.

Jayant Raikhelkar (J)

Section of Cardiology Department of Medicine University of Chicago IL.

Sara Kalantari (S)

Section of Cardiology Department of Medicine University of Chicago IL.

Bryan Smith (B)

Section of Cardiology Department of Medicine University of Chicago IL.

Nitasha Sarswat (N)

Section of Cardiology Department of Medicine University of Chicago IL.

Colleen LaBuhn (C)

Section of Cardiac Surgery Department of Surgery University of Chicago IL.

Valluvan Jeevanandam (V)

Section of Cardiac Surgery Department of Surgery University of Chicago IL.

Gene Kim (G)

Section of Cardiology Department of Medicine University of Chicago IL.

Gabriel Sayer (G)

Section of Cardiology Department of Medicine University of Chicago IL.

Nir Uriel (N)

Section of Cardiology Department of Medicine University of Chicago IL.

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Classifications MeSH