Ivabradine

Author:

Chaudhary Rahul1,Garg Jalaj2,Krishnamoorthy Parasuram3,Shah Neeraj2,Lanier Gregg4,Martinez Mathew W.2,Freudenberger Ronald2

Affiliation:

1. Department of Medicine, Sinai Hospital of Baltimore, Johns Hopkins University, Baltimore, MD, USA

2. Division of Cardiology, Lehigh Valley Health Network, Allentown, PA, USA

3. Department of Medicine, Englewood Hospital and Medical Center, Mount Sinai School of Medicine, Englewood, NJ, USA

4. Division of Cardiology, Westchester Medical Center, New York Medical College, Valhalla, NY, USA

Abstract

Heart failure affects over 5 million people in the United States and carries a high rate of mortality. Ivabradine, a new agent has been added to the current medical options for managing heart failure. It is a selective funny current ( If) inhibitor in sinoatrial node and slows its firing rate, prolonging diastolic depolarization without a negative inotropic effect. Ivabradine was only recently approved by Food and Drug administration after the results of Systolic Heart Failure Treatment with the If Inhibitor Ivabradine (SHIFT) trial, for a reduction in rehospitalizations from chronic heart failure. This trial assessed patients with stable heart failure with reduced ejection fraction and a heart rate of at least 70 beats per minute at rest on maximally tolerated beta-blocker therapy and demonstrated statistically significant reduction in heart failure hospitalization and deaths. Additionally, ivabradine has been associated with reduced cardiac remodeling, reduced heart rate variability, improvement in exercise tolerance, improved heart failure class of New York Heart Association, and better quality of life. It has also been tried in other conditions, such as inappropriate sinus tachycardia and cardiogenic shock, and is currently in phase II trial for patients with newly diagnosed multiple organ dysfunction syndrome.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine,Pharmacology

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