Treatment patterns of patients with worsening heart failure with reduced ejection fraction.

HFrEF Medical therapy Worsening heart failure

Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
19 Apr 2024
Historique:
revised: 28 02 2024
received: 26 09 2023
accepted: 25 03 2024
medline: 19 4 2024
pubmed: 19 4 2024
entrez: 19 4 2024
Statut: aheadofprint

Résumé

Patients with HFrEF and worsening HF events (WHFE) are at particularly high risk and urgently need disease-modifying therapy. CHART-HF assessed treatment patterns and reasons for medication decisions among HFrEF patients with and without WHFE. CHART-HF collected retrospective electronic medical records of outpatients with HF and EF < 45% between 2017-2019 from a nationwide panel of 238 cardiologists (458 patients) and the Geisinger Health System (GHS) medical record (1000 patients). The index visit in the WHFE cohort was the first outpatient cardiologist visit ≤6 months following the WHFE, and in the reference cohort was the last visit in a calendar year without WHFE. Demographic characteristics were similar between patients with and without WHFE in both the nationwide panel and GHS. In the nationwide panel, the proportion of patients with versus without WHFE receiving ≥50% of guideline-recommended dose on index visit was 35% versus 40% for beta blocker, 74% versus 83% for ACEI/ARB/ARNI, and 48% versus 49% for MRA. The proportion of patients receiving ≥50% of guideline-recommended dose was lower in the GHS: 29% versus 34% for beta-blocker, 16% versus 31% for ACEI/ARB/ARNI, and 18% versus 22% for MRA. For patients with and without WHFE, triple therapy on index date was 42% and 44% of patients from the nationwide panel, and 14% and 17% in the GHS. Comparing end of index clinic visit with 12-month follow-up in the GHS, the proportion of patients on no GDMT increased from 14% to 28% in the WHFE cohort and from 14 to 21% in the non-WHFE group. Major gaps in use of GDMT, particularly combination therapy, remain among US HFrEF patients. These gaps persist during longitudinal follow-up and are particularly large among patients with recent WHFE.

Identifiants

pubmed: 38639469
doi: 10.1002/ehf2.14805
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Merck Sharp & Dohme LLC

Informations de copyright

© 2024 Merck Sharp & Dohme LLC and The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Stephen J Greene (SJ)

Duke Clinical Research Institute, Durham, NC, USA.
Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.

Hanna K Gaggin (HK)

Harvard Medical School, Boston, MA, USA.
Division of Cardiology, Massachusetts General Hospital, Boston, MA, USA.

Mo Zhou (M)

Analysis Group, Inc., Boston, MA, USA.

Lori D Bash (LD)

Merck & Co., Inc., Rahway, NJ, USA.

Dominik Lautsch (D)

Merck & Co., Inc., Rahway, NJ, USA.

Laurence Djatche (L)

Merck & Co., Inc., Rahway, NJ, USA.

Yan Song (Y)

Analysis Group, Inc., Boston, MA, USA.

James Signorovitch (J)

Analysis Group, Inc., Boston, MA, USA.

Andra S Stevenson (AS)

Merck & Co., Inc., Rahway, NJ, USA.

Robert O Blaustein (RO)

Merck & Co., Inc., Rahway, NJ, USA.

Javed Butler (J)

Department of Medicine, University of Mississippi Medical Center, Jackson, MS, USA.
Baylor Scott and White Research Institute, Dallas, TX, USA.

Classifications MeSH