Literature DB >> 27780557

Benefits of Heart Rate Slowing With Ivabradine in Patients With Systolic Heart Failure and Coronary Artery Disease.

Jeffrey S Borer1, Prakash C Deedwania2, Jae B Kim3, Michael Böhm4.   

Abstract

Heart rate (HR) is a risk factor in patients with chronic systolic heart failure (HF) that, when reduced, provides outcome benefits. It is also a target for angina pectoris prevention and a risk marker in chronic coronary artery disease without HF. HR can be reduced by drugs; however, among those used clinically, only ivabradine reduces HR directly in the sinoatrial nodal cells without other known effects on the cardiovascular system. This review provides current information regarding the safety and efficacy of HR reduction with ivabradine in clinical studies involving >36,000 patients with chronic stable coronary artery disease and >6,500 patients with systolic HF. The largest trials, Morbidity-Mortality Evaluation of the If Inhibitor Ivabradine in Patients With Coronary Disease and Left Ventricular Dysfunction and Study Assessing the Morbidity-Mortality Benefits of the If Inhibitor Ivabradine in Patients With Coronary Artery Disease, showed no effect on outcomes. The Systolic Heart Failure Treatment With the If Inhibitor Ivabradine Trial, a randomized controlled trial in >6,500 patients with HF, revealed marked and significant HR-mediated reduction in cardiovascular mortality or HF hospitalizations while improving quality of life and left ventricular mechanical function after treatment with ivabradine. The adverse effects of ivabradine predominantly included bradycardia and atrial fibrillation (both uncommon) and ocular flashing scotomata (phosphenes) but otherwise were similar to placebo. In conclusion, ivabradine improves outcomes in patients with systolic HF; rates of overall adverse events are similar to placebo. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27780557     DOI: 10.1016/j.amjcard.2016.08.089

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  8 in total

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Authors:  Yingxin Li; Xiaoxiao Zhang; Chen Zhang; Xiaoying Zhang; Ying Li; Zhao Qi; Christopher Szeto; Mingxin Tang; Yizhi Peng; Jeffery D Molkentin; Steven R Houser; Mingxing Xie; Xiongwen Chen
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Review 4.  Optimization of Heart Failure Treatment by Heart Rate Reduction.

Authors:  Michael Böhm; Yvonne Bewarder; Ingrid Kindermann; Jonathan Slawik; Jan Wintrich; Christian Werner
Journal:  Int J Heart Fail       Date:  2019-12-09

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6.  Influences of Ivabradine treatment on serum levels of cardiac biomarkers sST2, GDF-15, suPAR and H-FABP in patients with chronic heart failure.

Authors:  Peter Jirak; Dzeneta Fejzic; Vera Paar; Bernhard Wernly; Rudin Pistulli; Ilonka Rohm; Christian Jung; Uta C Hoppe; P Christian Schulze; Michael Lichtenauer; Atilla Yilmaz; Daniel Kretzschmar
Journal:  Acta Pharmacol Sin       Date:  2017-12-14       Impact factor: 6.150

7.  Ivabradine as adjuvant treatment for chronic heart failure.

Authors:  Carina Benstoem; Christina Kalvelage; Thomas Breuer; Nicole Heussen; Gernot Marx; Christian Stoppe; Vincent Brandenburg
Journal:  Cochrane Database Syst Rev       Date:  2020-11-04

8.  Ivabradine improves survival and attenuates cardiac remodeling in isoproterenol-induced myocardial injury.

Authors:  Fedor Simko; Tomas Baka; Kristina Repova; Silvia Aziriova; Kristina Krajcirovicova; Ludovit Paulis; Michaela Adamcova
Journal:  Fundam Clin Pharmacol       Date:  2020-11-07       Impact factor: 2.748

  8 in total

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