Safety of Outpatient Milrinone Infusion in End-Stage Heart Failure: ICD-Level Data on Atrial Fibrillation and Ventricular Tachyarrhythmias.


Journal

The American journal of medicine
ISSN: 1555-7162
Titre abrégé: Am J Med
Pays: United States
ID NLM: 0267200

Informations de publication

Date de publication:
07 2020
Historique:
received: 13 11 2019
revised: 22 11 2019
accepted: 25 11 2019
pubmed: 31 12 2019
medline: 17 9 2020
entrez: 30 12 2019
Statut: ppublish

Résumé

Milrinone infusion is one of a few select "non-device" therapies for patients with New York Heart Association (NYHA) class IV, stage D heart failure, which has been associated with an increase in ventricular tachyarrhythmia and atrial fibrillation. Milrinone improves hemodynamics and provides symptomatic relief. Many patients with end-stage heart failure die from cardiac pump failure, and the impact of ventricular tachyarrhythmia and atrial fibrillation on their mortality is unclear. This is a retrospective study of 98 consecutive patients receiving outpatient milrinone in a single center from 2008 to 2016. The primary endpoint of the study was overall survival on milrinone. Secondary endpoints were incidence of post-milrinone implantable cardioverter defibrillator (ICD) shocks and development of ventricular tachyarrhythmia or atrial fibrillation. Median survival was 581 ± 96 days with no difference between those with prior ventricular tachyarrhythmia and those without at 1 month (92% vs 97%, P = 0.34), 6 months (67% vs 73%, P = 0.75), and 12 months (67% vs 61%, P = 0.88). Seven out of 12 (58%) patients with prior ventricular tachyarrhythmia had ICD shocks, as compared to 5 out of 78 (6.4%) (P <0.001). Thirty-five patients had atrial fibrillation prior to starting milrinone, which decreased to 72% (P <0.05) by the third follow-up time period (7-9 months). Amiodarone use was protective against new onset atrial fibrillation. Patients with stage D heart failure with a history of ventricular tachyarrhythmia have similar survival on outpatient milrinone compared to those without. However, those with prior ventricular tachyarrhythmia received more ICD shocks for more ventricular tachyarrhythmias. Milrinone remains a viable therapy for patients with stage D heart failure with limited therapeutic options.

Sections du résumé

BACKGROUND
Milrinone infusion is one of a few select "non-device" therapies for patients with New York Heart Association (NYHA) class IV, stage D heart failure, which has been associated with an increase in ventricular tachyarrhythmia and atrial fibrillation. Milrinone improves hemodynamics and provides symptomatic relief. Many patients with end-stage heart failure die from cardiac pump failure, and the impact of ventricular tachyarrhythmia and atrial fibrillation on their mortality is unclear.
METHODS
This is a retrospective study of 98 consecutive patients receiving outpatient milrinone in a single center from 2008 to 2016. The primary endpoint of the study was overall survival on milrinone. Secondary endpoints were incidence of post-milrinone implantable cardioverter defibrillator (ICD) shocks and development of ventricular tachyarrhythmia or atrial fibrillation.
RESULTS
Median survival was 581 ± 96 days with no difference between those with prior ventricular tachyarrhythmia and those without at 1 month (92% vs 97%, P = 0.34), 6 months (67% vs 73%, P = 0.75), and 12 months (67% vs 61%, P = 0.88). Seven out of 12 (58%) patients with prior ventricular tachyarrhythmia had ICD shocks, as compared to 5 out of 78 (6.4%) (P <0.001). Thirty-five patients had atrial fibrillation prior to starting milrinone, which decreased to 72% (P <0.05) by the third follow-up time period (7-9 months). Amiodarone use was protective against new onset atrial fibrillation.
CONCLUSIONS
Patients with stage D heart failure with a history of ventricular tachyarrhythmia have similar survival on outpatient milrinone compared to those without. However, those with prior ventricular tachyarrhythmia received more ICD shocks for more ventricular tachyarrhythmias. Milrinone remains a viable therapy for patients with stage D heart failure with limited therapeutic options.

Identifiants

pubmed: 31883773
pii: S0002-9343(19)31104-0
doi: 10.1016/j.amjmed.2019.11.023
pii:
doi:

Substances chimiques

Cardiotonic Agents 0
Milrinone JU9YAX04C7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

857-864

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Ahmed A Harhash (AA)

Morristown Medical Center, Morristown, NJ; University of Arizona Sarver Heart Center, Ariz. Electronic address: ahmedhrhsh@gmail.com.

James Cassuto (J)

Morristown Medical Center, Morristown, NJ.

Ahmed Hussein (A)

Morristown Medical Center, Morristown, NJ.

Emmanuel Achu (E)

Rutgers University, New Jersey Medical School, NJ.

Mark J Zucker (MJ)

Rutgers University, New Jersey Medical School, NJ.

Marc Goldschmidt (M)

Morristown Medical Center, Morristown, NJ.

Joseph S Alpert (JS)

Professor of Medicine, Department of Medicine, University of Arizona, Tucson; Editor in Chief, The American Journal of Medicine.

David A Baran (DA)

Sentara Heart Hospital, Norfolk, Va.

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Classifications MeSH