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Updated: Jul 10, 2026

Percutaneous Contrast Echocardiography-guided Intramyocardial Injection and Cell Delivery in a Large Preclinical Model
Published on: January 21, 2018
Clinical results of I(f) current inhibition by ivabradine
1Montreal Heart Institute, Montreal, Quebec, Canada. jean-claude.tardif@icm-mhi.org
Insights
Ivabradine effectively reduces heart rate to prevent angina pectoris. This pure heart rate reduction offers an alternative to traditional antianginal drugs with a favorable safety profile.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Heart rate reduction is a proven strategy for preventing angina pectoris.
- Ivabradine selectively inhibits the I(f) current, lowering heart rate without affecting myocardial contractility.
Purpose of the Study:
- To evaluate the antianginal and anti-ischaemic efficacy and tolerability of ivabradine.
- To compare ivabradine's effectiveness against established antianginal treatments.
Main Methods:
- Clinical development program involving over 5000 patients with stable angina pectoris.
- Dosages of 5 or 7.5mg of ivabradine administered twice daily.
- 1-year follow-up study to confirm long-term efficacy and safety.
Main Results:
- Ivabradine demonstrated efficacy comparable to beta-blockers and calcium channel blockers.
- The drug was well-tolerated, with a notable absence of common adverse effects associated with other antianginal medications.
- Visual disturbances were reported in a small patient subset but without ocular structural changes.
Conclusions:
- Ivabradine is a safe and effective option for managing stable angina pectoris.
- Its unique mechanism offers pure heart rate reduction, distinguishing it from other antianginal therapies.
- Ongoing studies (BEAUTIFUL, SHIfT) may expand its use in coronary artery disease and heart failure populations.
Abstract:
Heart rate reduction is a well accepted and effective approach for the prevention of angina pectoris. Ivabradine is the first selective and specific inhibitor of the I(f) current and provides pure heart rate reduction without altering myocardial contractility. Clinical evidence of the antianginal and anti-ischaemic efficacy and tolerability of ivabradine comes from the largest clinical development programme that has ever been performed in stable angina pectoris, involving more than 5000 patients. Ivabradine at the dosages of 5 or 7.5mg twice daily is as effective as reference antianginal approaches such as beta-adrenoceptor antagonists and calcium channel antagonists. The clinical efficacy and safety of ivabradine has also been confirmed in a 1-year follow-up study. Ivabradine is well tolerated and free from the most commonly observed adverse effects of currently prescribed antianginal drugs. Visual symptoms can occur in a minority of patients treated with ivabradine and are not associated with structural ocular changes. The ongoing clinical development programme with the two major morbidity-mortality studies, BEAUTIFUL and SHIfT, has the potential to greatly extend the use of ivabradine in patients with coronary artery disease as well as in those with heart failure.
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