Characteristics and Outcomes of Suspected Digoxin Toxicity and Immune Fab Treatment Over the Past Two Decades-2000-2020.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
15 11 2022
Historique:
received: 11 04 2022
revised: 25 07 2022
accepted: 06 08 2022
pubmed: 12 9 2022
medline: 19 10 2022
entrez: 11 9 2022
Statut: ppublish

Résumé

The role of digoxin in clinical practice has narrowed over time. Data on digoxin toxicity trends and outcomes are variable and lack granularity for treatment outcomes. This study aimed to address data gaps in digoxin toxicity trends and outcomes in patients treated with or without digoxin immune fab (DIF). This single-center analysis examined patients with signs/symptoms concerning digoxin toxicity, defined as hospital admission or emergency department visit with elevated digoxin serum concentrations (>2 ng/ml) and/or a primary diagnosis code of digoxin toxicity and/or DIF order. Between 2000 and 2020, 727 patients were identified with signs concerning for digoxin toxicity with a mortality rate of 12.7% during admission and 42.7% at 1 year. DIF was ordered in 9% of cases. Incidence of digoxin toxicity per 1,000 patients with a digoxin prescription and frequency of DIF treatment fluctuated over time without a clear trend toward increase or reduction. DIF-treated patients demonstrated a heavier co-morbidity burden and lower presenting heart rates (median 53 [39.5 to 69.5] vs 77 [64.0 to 91.5] beats/min, p <0.001), worse renal function (median estimated glomerular filtration rate, 30.3 [14.8 to 48.6] vs 40.0 [24.2 to 61.2] ml/min/1.73 m

Identifiants

pubmed: 36089419
pii: S0002-9149(22)00836-0
doi: 10.1016/j.amjcard.2022.08.004
pmc: PMC9588603
mid: NIHMS1840780
pii:
doi:

Substances chimiques

Cardiovascular Agents 0
Digoxin 73K4184T59
Potassium RWP5GA015D
Immunoglobulin Fab Fragments 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

129-136

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL069749
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL150159
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL151744
Pays : United States

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosures Dr. Ambrosy has received relevant research support through grants to his institution from Amarin Pharma, Inc., Abbott, and Novartis; and has received modest reimbursement for travel from Novartis. Dr. Fudim receives consulting fees from Abbott, Audicor, AxonTherapies, Bodyguide, Bodyport, Boston Scientific, CVRx, Daxor, Edwards Lifesciences, Feldschuh Foundation, Fire1, Gradient, Intershunt, NXT Biomedical, Pharmacosmos, PreHealth, Shifamed, Splendo, Vironix, Viscardia, and Zoll. The remaining authors have no conflicts of interest to declare.

Références

Am J Med. 2019 Oct;132(10):1191-1198
pubmed: 31077654
BMJ. 2015 Aug 30;351:h4451
pubmed: 26321114
Am J Cardiol. 2019 Jan 1;123(1):69-74
pubmed: 30539748
Circulation. 1990 Jun;81(6):1744-52
pubmed: 2188752
Eur Heart J. 2015 Jul 21;36(28):1831-8
pubmed: 25939649
JACC Heart Fail. 2016 May;4(5):357-64
pubmed: 27039127
Circ Heart Fail. 2014 Jan;7(1):28-34
pubmed: 24300242
Clin Toxicol (Phila). 2014 Sep-Oct;52(8):824-36
pubmed: 25089630
J Am Coll Cardiol. 2013 Oct 15;62(16):e147-239
pubmed: 23747642
Drugs Real World Outcomes. 2021 Jun;8(2):253-262
pubmed: 33721285
JAMA. 2021 Apr 27;325(16):1681-1682
pubmed: 33904873
J Card Fail. 2006 Jun;12(5):343-6
pubmed: 16762795
Clin Pharmacol Ther. 2008 Jul;84(1):90-4
pubmed: 18091761
Am J Med. 1974 Jul;57(1):63-8
pubmed: 4600984
Am Heart J. 2018 May;199:97-104
pubmed: 29754673
JAMA. 2020 Dec 22;324(24):2497-2508
pubmed: 33351042

Auteurs

Anthony E Peters (AE)

Division of Cardiology, Department of Medicine; Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Karen Chiswell (K)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Paul Hofmann (P)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.

Andrew Ambrosy (A)

Department of Cardiology, Kaiser Permanente San Francisco Medical Center, San Francisco, California; Division of Research, Kaiser Permanente Northern California, Oakland, California.

Marat Fudim (M)

Division of Cardiology, Department of Medicine; Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina. Electronic address: marat.fudim@duke.edu.

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Classifications MeSH