Real-World Efficacy of Tafamidis in Patients With Transthyretin Amyloidosis and Heart Failure.


Journal

Current problems in cardiology
ISSN: 1535-6280
Titre abrégé: Curr Probl Cardiol
Pays: Netherlands
ID NLM: 7701802

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 12 02 2023
accepted: 17 02 2023
medline: 1 5 2023
pubmed: 25 2 2023
entrez: 24 2 2023
Statut: ppublish

Résumé

Tafamidis was associated with a reduction in cardiovascular hospitalizations and all-cause mortality in patients with transthyretin amyloid cardiomyopathy (ATTR-CM) in the ATTR-ACT trial. However, real-world data on the efficacy of tafamidis are limited. We conducted a retrospective, observational cohort study using the TriNetX research network. Patients with wild-type TTR amyloidosis and heart failure (HF) were divided into 2 groups based on treatment with tafamidis. Propensity score matching (PSM) was performed, and rates of heart failure exacerbations (HFE) and all-cause mortality at 12 months were compared. After PSM, 421 patients were in each group (tafamidis vs nontafamidis). During the 12-month follow-up period, patients treated with tafamidis experienced significantly less HFE and all-cause mortality. A higher probability of event-free survival for HFE and all-cause mortality was noted with tafamidis. This real-world analysis supports that tafamidis use is associated with reduced HFE and all-cause mortality in patients with wild-type TTR amyloidosis and HF. Longer-term follow-up is needed to better understand the utility of tafamidis, given the increasing recognition of ATTR-CM and the high cost of tafamidis.

Identifiants

pubmed: 36828040
pii: S0146-2806(23)00084-1
doi: 10.1016/j.cpcardiol.2023.101667
pii:
doi:

Substances chimiques

tafamidis 8FG9H9D31J
Prealbumin 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

101667

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Ahmed Ghoneem (A)

Lahey Hospital and Medical Center, Burlington, MA.

Ammar W Bhatti (AW)

Lahey Hospital and Medical Center, Burlington, MA.

Sumanth Khadke (S)

Lahey Hospital and Medical Center, Burlington, MA.

Joshua Mitchell (J)

Washington University Medical Campus, St. Louis, MO.

Jennifer Liu (J)

Memorial Sloan Kettering Cancer Center, New York, NY.

Kathleen Zhang (K)

University of Texas Southwestern Medical Center, Dallas, TX.

Barry Trachtenberg (B)

Houston Methodist Hospital, Houston, TX.

Ashutosh Wechalekar (A)

University College of London, London, UK.

Richard K Cheng (RK)

University of Washington Medical Center, Seattle, WA.

Suzanne J Baron (SJ)

Lahey Hospital and Medical Center, Burlington, MA; Baim Institute for Clinical Research, Boston, MA.

Anju Nohria (A)

Brigham and Women's Hospital, Boston, MA.

Daniel Lenihan (D)

Washington University School of Medicine, St. Louis, MO.

Sarju Ganatra (S)

Lahey Hospital and Medical Center, Burlington, MA. Electronic address: Sarju.Ganatra@Lahey.org.

Sourbha S Dani (SS)

Lahey Hospital and Medical Center, Burlington, MA.

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Classifications MeSH