Safety of Diltiazem for Acute Management of Atrial Fibrillation (AF) in Patients with Heart Failure and Reduced Ejection Fraction in the Emergency Department.

Atrial fibrillation Calcium channel blocker Diltiazem Emergency department Heart failure

Journal

The Journal of emergency medicine
ISSN: 0736-4679
Titre abrégé: J Emerg Med
Pays: United States
ID NLM: 8412174

Informations de publication

Date de publication:
13 Jun 2024
Historique:
received: 29 10 2023
revised: 21 04 2024
accepted: 08 06 2024
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 1 10 2024
Statut: aheadofprint

Résumé

Diltiazem is an effective rate control agent for atrial fibrillation with rapid ventricular rate (AF RVR). However, its negative inotropic effects may increase the risk for worsening heart failure in patients with a reduced ejection fraction (EF). This observational study aims to describe the incidence of worsening heart failure in patients who receive intravenous diltiazem for acute atrial fibrillation management. Adult patients that received diltiazem in the emergency department (ED) for AF RVR (heart rate ≥ 100 beats/min) from 2021 to 2022 and had a prior documented EF were included. The primary outcome is worsening heart failure within 24 h of diltiazem administration. Secondary outcomes include return ED visits and death within 7 days. EF percentage was compared across outcomes using Wilcoxon rank-sum tests. Outcomes were compared by reduced EF (< 50%) and preserved EF (≥ 50%). Continuous data were summarized with medians and interquartile ranges, and categorical features were summarized with frequency counts and percentages. Wilcoxon rank-sum tests were used for numeric outcomes and chi-squared tests or Fisher's exact tests for categorical outcomes, with a p-value < 0.05 considered statistically significant. There were 674 patients with AF RVR that received diltiazem, and 386 patients met the inclusion criteria for analysis. Baseline demographics included a median age of 72 (64-81) years, with 14.5% of patients having a prior diagnosis of congestive heart failure. EF < 50% was identified in 13.7% of patients (n = 53), of which approximately 30% of these patients safely discharged home after receiving i.v. diltiazem. The primary outcome of worsening heart failure occurred in 7/41 (17%) and 10/207 (4.8%) patients with reduced and preserved ejection fractions, respectively, who were admitted to the hospital (p = 0.005). The development of worsening heart failure is multifactorial and may include the use of diltiazem in critically ill patients requiring hospital admission.

Sections du résumé

BACKGROUND BACKGROUND
Diltiazem is an effective rate control agent for atrial fibrillation with rapid ventricular rate (AF RVR). However, its negative inotropic effects may increase the risk for worsening heart failure in patients with a reduced ejection fraction (EF).
OBJECTIVES OBJECTIVE
This observational study aims to describe the incidence of worsening heart failure in patients who receive intravenous diltiazem for acute atrial fibrillation management.
METHODS METHODS
Adult patients that received diltiazem in the emergency department (ED) for AF RVR (heart rate ≥ 100 beats/min) from 2021 to 2022 and had a prior documented EF were included. The primary outcome is worsening heart failure within 24 h of diltiazem administration. Secondary outcomes include return ED visits and death within 7 days. EF percentage was compared across outcomes using Wilcoxon rank-sum tests. Outcomes were compared by reduced EF (< 50%) and preserved EF (≥ 50%). Continuous data were summarized with medians and interquartile ranges, and categorical features were summarized with frequency counts and percentages. Wilcoxon rank-sum tests were used for numeric outcomes and chi-squared tests or Fisher's exact tests for categorical outcomes, with a p-value < 0.05 considered statistically significant.
RESULTS RESULTS
There were 674 patients with AF RVR that received diltiazem, and 386 patients met the inclusion criteria for analysis. Baseline demographics included a median age of 72 (64-81) years, with 14.5% of patients having a prior diagnosis of congestive heart failure. EF < 50% was identified in 13.7% of patients (n = 53), of which approximately 30% of these patients safely discharged home after receiving i.v. diltiazem. The primary outcome of worsening heart failure occurred in 7/41 (17%) and 10/207 (4.8%) patients with reduced and preserved ejection fractions, respectively, who were admitted to the hospital (p = 0.005).
CONCLUSION CONCLUSIONS
The development of worsening heart failure is multifactorial and may include the use of diltiazem in critically ill patients requiring hospital admission.

Identifiants

pubmed: 39353791
pii: S0736-4679(24)00210-5
doi: 10.1016/j.jemermed.2024.06.010
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Cassandra J Schmitt (CJ)

Department of Pharmacy, Mayo Clinic, Rochester, Minnesota.

Alicia E Mattson (AE)

Department of Pharmacy, Mayo Clinic, Rochester, Minnesota.

Daniel Cabrera (D)

Department of Emergency Medicine, Mayo Clinic, Rochester, Minnesota.

Aidan Mullan (A)

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota.

Coral Marí Chantada (C)

San Juan Bautista School of Medicine, Caguas, Puerto Rico.

Annelise S Howick (AS)

Department of Emergency Medicine, Mayo Clinic, Rochester, Minnesota.

Garvan C Kane (GC)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota.

Fernanda Bellolio (F)

Department of Emergency Medicine, Mayo Clinic, Rochester, Minnesota; Department of Health Care Delivery Research, Mayo Clinic, Rochester, Minnesota; Department of Medicine, Division of Community Internal Medicine, Palliative Care and Geriatrics, Mayo Clinic, Rochester, Minnesota.

Classifications MeSH