Literature DB >> 21434947

Innovation in coronary artery disease and heart failure: clinical benefits of pure heart rate reduction with ivabradine.

Emmanuel Canet1, Guy Lerebours, Jean-Paul Vilaine.   

Abstract

The link between elevated heart rate and cardiovascular events is established in healthy individuals and in patients with cardiovascular disease. The new agent, ivabradine, specifically and selectively inhibits the I(f) current, with the sole action of heart rate reduction, with no impact on any other cardiac parameters. The benefits of "pure" heart rate reduction with ivabradine have been the focus of one of the largest clinical development programs ever performed, involving >20,000 individuals. Ivabradine has anti-ischemic and antianginal efficacy in monotherapy, as well as in combination with other antianginals, such as beta-blockers, and is safe and well tolerated. Two major morbidity-mortality trials, BEAUTIFUL and SHIFT, showed that heart rate reduction with ivabradine dramatically improves prognosis in patients with coronary artery disease and left ventricular dysfunction, symptomatic angina, or chronic heart failure. The development of ivabradine represents a clear innovation in the management of cardiovascular disease.
© 2011 New York Academy of Sciences.

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Year:  2011        PMID: 21434947     DOI: 10.1111/j.1749-6632.2011.05960.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  8 in total

1.  Complementary and Synergic Role of Combined Beta-blockers and Ivabradine in Patients with Chronic Heart Failure and Depressed Systolic Function: A New Therapeutic Option?

Authors:  Maurizio Volterrani; Ferdinando Iellamo
Journal:  Card Fail Rev       Date:  2016-11

2.  Downregulation of autophagy-related circular RNA (ACR) is correlated with poor survival of patients with chronic heart failure.

Authors:  Haihui Yan; Dan Du; Chen Wang; Miao Tian
Journal:  Bioengineered       Date:  2022-05       Impact factor: 6.832

3.  Inducible re-expression of HEXIM1 causes physiological cardiac hypertrophy in the adult mouse.

Authors:  Monica M Montano; Candida L Desjardins; Yong Qui Doughman; Yee-Hsee Hsieh; Yanduan Hu; Heather M Bensinger; Connie Wang; Julian E Stelzer; Thomas E Dick; Brian D Hoit; Margaret P Chandler; Xin Yu; Michiko Watanabe
Journal:  Cardiovasc Res       Date:  2013-04-11       Impact factor: 10.787

4.  Treatment of subclinical hyperthyroidism: effect on left ventricular mass and function of the heart using magnetic resonance imaging technique.

Authors:  Peter D Mark; Mikkel Andreassen; Claus L Petersen; Andreas Kjaer; Jens Faber
Journal:  Endocr Connect       Date:  2015-01-07       Impact factor: 3.335

Review 5.  Selective and specific inhibition of If with ivabradine for the treatment of coronary artery disease or heart failure.

Authors:  Prakash Deedwania
Journal:  Drugs       Date:  2013-09       Impact factor: 9.546

Review 6.  Ivabradine, coronary artery disease, and heart failure: beyond rhythm control.

Authors:  Pietro Scicchitano; Francesca Cortese; Gabriella Ricci; Santa Carbonara; Michele Moncelli; Massimo Iacoviello; Annagrazia Cecere; Michele Gesualdo; Annapaola Zito; Pasquale Caldarola; Domenico Scrutinio; Rocco Lagioia; Graziano Riccioni; Marco Matteo Ciccone
Journal:  Drug Des Devel Ther       Date:  2014-06-03       Impact factor: 4.162

Review 7.  Role of ivabradine in management of stable angina in patients with different clinical profiles.

Authors:  Juan Carlos Kaski; Steffen Gloekler; Roberto Ferrari; Kim Fox; Bernard I Lévy; Michel Komajda; Panos Vardas; Paolo G Camici
Journal:  Open Heart       Date:  2018-03-09

Review 8.  Ivabradine: an intelligent drug for the treatment of ischemic heart disease.

Authors:  Graziano Riccioni
Journal:  Molecules       Date:  2012-11-16       Impact factor: 4.411

  8 in total

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