Literature DB >> 8547212

Digoxin and mortality in survivors of acute myocardial infarction: observations in patients at low and intermediate risk. The SPRINT Study Group. Secondary Prevention Reinfarction Israeli Nifedipine Trial.

J Leor1, U Goldbourt, S Behar, V Boyko, H Reicher-Reiss, E Kaplinsky, B Rabinowitz.   

Abstract

Controversy surrounds the safety of digoxin use in patients recovering from acute myocardial infarction. Previous observations yielded contradictory conclusions. To determine whether digoxin therapy is associated with increased mortality in patients recovering from acute myocardial infarction, we analyzed data from 1731 survivors of acute myocardial infarction enrolled in the Secondary Prevention Reinfarction Israeli Nifedipine Trial (SPRINT), from which patients with severe heart failure were excluded. At the time of hospital discharge, 175 patients (10%) were taking digoxin. Mortality over 1 year after infarction was significantly higher in patients treated with digoxin than in patients who were not receiving digoxin [27 of 175 (15%) vs. 60 of 1556 (4%); p < 0.0001]. Digoxin administration was associated with increased mortality in several subsets of patients. Since patients treated with digoxin had baseline characteristics predictive of mortality more frequently than their counterparts, we adjusted for these differences. Multivariate analysis performed by the Cox proportional hazards model identified treatment with digoxin as an independent determinant associated with increased death during the first year after myocardial infarction [relative risk (RR) 2.8; 90% confidence interval (CI) 1.8-4.2]. Subgroup multivariate analysis indicated digoxin as an independent predictor of first year death in 464 patients who developed heart failure during their hospital stay (RR 2.3; 90% CI 1.3-4.0), as well as among 1267 patients who did not (RR 3.4; 90% CI 1.7-6.9). The present study suggests a significant excess mortality associated with digoxin therapy after myocardial infarction. The increased mortality risk may be related to unidentified variables associated with the severity of disease in patients treated with digoxin. However, our findings raise concern that the administration of digoxin may contribute to increased mortality in survivors of acute myocardial infarction.

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Year:  1995        PMID: 8547212     DOI: 10.1007/bf00878094

Source DB:  PubMed          Journal:  Cardiovasc Drugs Ther        ISSN: 0920-3206            Impact factor:   3.727


  26 in total

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Journal:  Am J Cardiol       Date:  1992-12-01       Impact factor: 2.778

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Journal:  Lancet       Date:  1992-11-14       Impact factor: 79.321

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  6 in total

1.  Membrane potential-dependent inhibition of the Na+,K+-ATPase by para-nitrobenzyltriethylammonium bromide.

Authors:  R Daniel Peluffo; Joshua R Berlin
Journal:  Mol Pharmacol       Date:  2012-03-28       Impact factor: 4.436

2.  QT interval dynamics and heart rate variability preceding a case of cardiac arrest.

Authors:  J P Singh; P Sleight; A Kardos; G Hart
Journal:  Heart       Date:  1997-04       Impact factor: 5.994

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Authors:  T A Fischer; N Treese
Journal:  Med Klin (Munich)       Date:  1997-09-15

4.  Digoxin: A systematic review in atrial fibrillation, congestive heart failure and post myocardial infarction.

Authors:  Sebastiano Virgadamo; Richard Charnigo; Yousef Darrat; Gustavo Morales; Claude S Elayi
Journal:  World J Cardiol       Date:  2015-11-26

5.  Digoxin use and outcomes after myocardial infarction in patients with atrial fibrillation.

Authors:  Ville Kytö; Antti Saraste; Päivi Rautava; Aleksi Tornio
Journal:  Basic Clin Pharmacol Toxicol       Date:  2022-04-22       Impact factor: 3.688

Review 6.  Safety and efficacy of digoxin: systematic review and meta-analysis of observational and controlled trial data.

Authors:  Oliver J Ziff; Deirdre A Lane; Monica Samra; Michael Griffith; Paulus Kirchhof; Gregory Y H Lip; Richard P Steeds; Jonathan Townend; Dipak Kotecha
Journal:  BMJ       Date:  2015-08-30
  6 in total

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