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Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure

OBJECTIVES: Ivabradine is a pharmacological agent used in patients with heart failure and sinus rhythm. Its only known pharmacological effect is to slow the heart rate. In this study, we investigated the impact of ivabradine on dyssynchrony parameters in heart failure patients. METHODS: In this stud...

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Autores principales: Soylu, Korhan, Cerik, Idris Bugra, Aksan, Gokhan, Nar, Gokay, Meric, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411195/
https://www.ncbi.nlm.nih.gov/pubmed/32782651
http://dx.doi.org/10.1002/joa3.12398
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author Soylu, Korhan
Cerik, Idris Bugra
Aksan, Gokhan
Nar, Gokay
Meric, Murat
author_facet Soylu, Korhan
Cerik, Idris Bugra
Aksan, Gokhan
Nar, Gokay
Meric, Murat
author_sort Soylu, Korhan
collection PubMed
description OBJECTIVES: Ivabradine is a pharmacological agent used in patients with heart failure and sinus rhythm. Its only known pharmacological effect is to slow the heart rate. In this study, we investigated the impact of ivabradine on dyssynchrony parameters in heart failure patients. METHODS: In this study, we assigned 55 patients taking medication for heart failure to receive ivabradine in addition (Group I). Twenty healthy volunteers comprised Group II. Echocardiographic measurements (dyssynchrony, left ventricular volumes and left ventricular ejection fraction) were taken at baseline, 1 month, and 3 months. RESULTS: A total of 32 heart failure patients in Group I completed the study. There was significant improvement in dyssynchrony parameters after ivabradine treatment in Group I. Interventricular dyssynchrony (IVD) decreased from 42.0 ± 24.4 milliseconds at baseline to 33.6 ± 20.7 milliseconds at 1 month (P = .001) and to 30.7 ± 19.4 milliseconds at 3 months (P < .001). Septal to posterior wall motion delay decreased from 90.3 ± 21.4 milliseconds to 83.9 ± 26.9 milliseconds (P = .011) at 1 month and to 81.5 ± 27.3 milliseconds at 3 months (P = .001). Septal to lateral Ts delay (Ts‐SL) decreased from 42.7 ± 24.5 milliseconds to 35.8 ± 22.6 milliseconds at 1 month (P < .001) and to 34.8 ± 22.4 milliseconds at 3 months (P = .002). Left ventricular end‐systolic volume (LVESV) decreased from 139.4 ± 42.2 mL to 135.3 ± 39.6 mL at 1 month (P = .006) and to 123.3 ± 39.5 mL at 3 months (P < .001). CONCLUSION: The addition of ivabradine to heart failure treatment improves cardiac dyssynchrony parameters in chronic systolic heart failure patients with sinus rhythm.
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spelling pubmed-74111952020-08-10 Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure Soylu, Korhan Cerik, Idris Bugra Aksan, Gokhan Nar, Gokay Meric, Murat J Arrhythm Original Articles OBJECTIVES: Ivabradine is a pharmacological agent used in patients with heart failure and sinus rhythm. Its only known pharmacological effect is to slow the heart rate. In this study, we investigated the impact of ivabradine on dyssynchrony parameters in heart failure patients. METHODS: In this study, we assigned 55 patients taking medication for heart failure to receive ivabradine in addition (Group I). Twenty healthy volunteers comprised Group II. Echocardiographic measurements (dyssynchrony, left ventricular volumes and left ventricular ejection fraction) were taken at baseline, 1 month, and 3 months. RESULTS: A total of 32 heart failure patients in Group I completed the study. There was significant improvement in dyssynchrony parameters after ivabradine treatment in Group I. Interventricular dyssynchrony (IVD) decreased from 42.0 ± 24.4 milliseconds at baseline to 33.6 ± 20.7 milliseconds at 1 month (P = .001) and to 30.7 ± 19.4 milliseconds at 3 months (P < .001). Septal to posterior wall motion delay decreased from 90.3 ± 21.4 milliseconds to 83.9 ± 26.9 milliseconds (P = .011) at 1 month and to 81.5 ± 27.3 milliseconds at 3 months (P = .001). Septal to lateral Ts delay (Ts‐SL) decreased from 42.7 ± 24.5 milliseconds to 35.8 ± 22.6 milliseconds at 1 month (P < .001) and to 34.8 ± 22.4 milliseconds at 3 months (P = .002). Left ventricular end‐systolic volume (LVESV) decreased from 139.4 ± 42.2 mL to 135.3 ± 39.6 mL at 1 month (P = .006) and to 123.3 ± 39.5 mL at 3 months (P < .001). CONCLUSION: The addition of ivabradine to heart failure treatment improves cardiac dyssynchrony parameters in chronic systolic heart failure patients with sinus rhythm. John Wiley and Sons Inc. 2020-07-05 /pmc/articles/PMC7411195/ /pubmed/32782651 http://dx.doi.org/10.1002/joa3.12398 Text en © 2020 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of Japanese Heart Rhythm Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Soylu, Korhan
Cerik, Idris Bugra
Aksan, Gokhan
Nar, Gokay
Meric, Murat
Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
title Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
title_full Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
title_fullStr Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
title_full_unstemmed Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
title_short Evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
title_sort evaluation of ivabradine in left ventricular dyssynchrony and reverse remodeling in patients with chronic heart failure
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411195/
https://www.ncbi.nlm.nih.gov/pubmed/32782651
http://dx.doi.org/10.1002/joa3.12398
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