Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation
© 2016 Elsevier Ireland Ltd Background It has been shown that I f channels can be found in AV node, apart from the sinus node. Previous animal studies showed that I f inhibitor resulted in the rate-dependent reduction in AV node conduction during atrial fibrillation (AF). Therefore, we aimed to ex...
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th-cmuir.6653943832-412232017-09-28T04:20:00Z Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation Wongcharoen W. Ruttanaphol A. Gunaparn S. Phrommintikul A. © 2016 Elsevier Ireland Ltd Background It has been shown that I f channels can be found in AV node, apart from the sinus node. Previous animal studies showed that I f inhibitor resulted in the rate-dependent reduction in AV node conduction during atrial fibrillation (AF). Therefore, we aimed to examine the effect of ivabradine on ventricular rate in patients with non-paroxysmal AF. Method This study was a prospective randomized, double blind, placebo-controlled study. Ivabradine, 5 mg twice a day (n = 21), or placebo (n = 11) was administered for 1 month to adult patients with non-paroxysmal AF, in addition to standard therapy. The primary end point was the change in mean ventricular rate between baseline and 1 month, as assessed by 24-hour Holter. Results The baseline characteristics did not differ between ivabradine and placebo groups (mean age was 59.7 ± 13.3 years, male 62.5%). Mean 24-hour ventricular rate at baseline was comparable between 2 groups. We found that ivabradine significantly decreased mean ventricular rate from 86.0 ± 10.9 beats/min to 79.2 ± 9.6 beats/min (p < 0.001). In contrast, no significant change in ventricular rate was observed in placebo group (84.3 ± 11.2 vs. 82.9 ± 9.9 beats/min, p = 0.469). The effect of ivabradine on rate reduction was significantly greater than placebo (6.9 ± 6.3 vs. 1.4 ± 6.0 beats/min, p = 0.024). No drug-related adverse effects were observed in both groups. Conclusion We demonstrated that ivabradine significantly decreased ventricular rate during AF compared to placebo. Therefore, ivabradine can be a potential treatment to improve ventricular control in patients with non-paroxysmal AF. Due to the small sample size, larger studies are needed to confirm this effect of ivabradine. 2017-09-28T04:20:00Z 2017-09-28T04:20:00Z 2016-12-01 Journal 01675273 2-s2.0-84988378432 10.1016/j.ijcard.2016.09.044 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84988378432&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41223 |
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© 2016 Elsevier Ireland Ltd Background It has been shown that I f channels can be found in AV node, apart from the sinus node. Previous animal studies showed that I f inhibitor resulted in the rate-dependent reduction in AV node conduction during atrial fibrillation (AF). Therefore, we aimed to examine the effect of ivabradine on ventricular rate in patients with non-paroxysmal AF. Method This study was a prospective randomized, double blind, placebo-controlled study. Ivabradine, 5 mg twice a day (n = 21), or placebo (n = 11) was administered for 1 month to adult patients with non-paroxysmal AF, in addition to standard therapy. The primary end point was the change in mean ventricular rate between baseline and 1 month, as assessed by 24-hour Holter. Results The baseline characteristics did not differ between ivabradine and placebo groups (mean age was 59.7 ± 13.3 years, male 62.5%). Mean 24-hour ventricular rate at baseline was comparable between 2 groups. We found that ivabradine significantly decreased mean ventricular rate from 86.0 ± 10.9 beats/min to 79.2 ± 9.6 beats/min (p < 0.001). In contrast, no significant change in ventricular rate was observed in placebo group (84.3 ± 11.2 vs. 82.9 ± 9.9 beats/min, p = 0.469). The effect of ivabradine on rate reduction was significantly greater than placebo (6.9 ± 6.3 vs. 1.4 ± 6.0 beats/min, p = 0.024). No drug-related adverse effects were observed in both groups. Conclusion We demonstrated that ivabradine significantly decreased ventricular rate during AF compared to placebo. Therefore, ivabradine can be a potential treatment to improve ventricular control in patients with non-paroxysmal AF. Due to the small sample size, larger studies are needed to confirm this effect of ivabradine. |
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Wongcharoen W. Ruttanaphol A. Gunaparn S. Phrommintikul A. |
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Wongcharoen W. Ruttanaphol A. Gunaparn S. Phrommintikul A. Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
author_facet |
Wongcharoen W. Ruttanaphol A. Gunaparn S. Phrommintikul A. |
author_sort |
Wongcharoen W. |
title |
Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
title_short |
Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
title_full |
Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
title_fullStr |
Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
title_full_unstemmed |
Ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
title_sort |
ivabradine reduced ventricular rate in patients with non-paroxysmal atrial fibrillation |
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2017 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84988378432&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41223 |
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