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A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study
OBJECTIVE: The aim of this prospective observational study was to evaluate the efficiency of a new escalating treatment strategy with vernakalant, flecainide and electrical cardioversion (EC) in patients with new onset atrial fibrillation (AF) after cardiac surgery. MATERIAL AND METHODS: 24 patients...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045875/ https://www.ncbi.nlm.nih.gov/pubmed/24886207 http://dx.doi.org/10.1186/1749-8090-9-83 |
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author | Zeriouh, Mohamed Sabashnikov, Anton Choi, Yeong-Hoon Fatullayev, Javid Reuter, Hannes Popov, Aron-Frederik Langebartels, Georg Kimmig, Lucas Rahmanian, Parwis B Wittwer, Thorsten Neef, Klaus Wippermann, Jens Wahlers, Thorsten |
author_facet | Zeriouh, Mohamed Sabashnikov, Anton Choi, Yeong-Hoon Fatullayev, Javid Reuter, Hannes Popov, Aron-Frederik Langebartels, Georg Kimmig, Lucas Rahmanian, Parwis B Wittwer, Thorsten Neef, Klaus Wippermann, Jens Wahlers, Thorsten |
author_sort | Zeriouh, Mohamed |
collection | PubMed |
description | OBJECTIVE: The aim of this prospective observational study was to evaluate the efficiency of a new escalating treatment strategy with vernakalant, flecainide and electrical cardioversion (EC) in patients with new onset atrial fibrillation (AF) after cardiac surgery. MATERIAL AND METHODS: 24 patients with new onset AF after aortic valve surgery, coronary artery bypass surgery or combined procedures were evaluated in this study. Additional including criteria were age between 18 and 80, duration of AF less than four days, body weight less than 100 kg and no previous treatment with class I or III antiarrhythmic drugs. Exclusion criteria were poor left ventricular ejection fraction (LVEF < 40%) and history of myocardial infarction within 30 days. The patients were divided into converters and non-converters according to their response to combination treatment with vernakalant and flecainide, and the groups were compared. RESULTS: The mean age of the population was 69.6 ± 6.3 years and 26.1% of patients were female. There were no statistically significant differences between the two groups in terms of height, weight, gender distribution, comorbidities, preoperative medication, left ventricular function and left atrium diameter. Interventricular septum (IVS) in the non-converted group was significantly thicker compared to the converted group: 14.0 ± 1.00 vs. 10.40 ± 2.59 mm (p = 0.036). While 14 patients (60.9%) were successfully converted into stable sinus rhythm by pharmacological treatment with vernakalant and flecainide, 9 patients (39.1%, non-converted group) remained in AF. However, seven of them could be converted after additional EC. CONCLUSION: The combination of vernakalant and flecainide improves the conversion rate into a stable sinus rhythm in postcardiotomy patients with new onset AF compared to single drug therapy. Furthermore it might be an excellent precondition for successful EC in patients who are not converted after using both antiarrhtythmic drugs. Furthermore, left ventricular hypertrophy might be a potential negative predictor of successful pharmacological cardioversion. |
format | Online Article Text |
id | pubmed-4045875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40458752014-06-06 A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study Zeriouh, Mohamed Sabashnikov, Anton Choi, Yeong-Hoon Fatullayev, Javid Reuter, Hannes Popov, Aron-Frederik Langebartels, Georg Kimmig, Lucas Rahmanian, Parwis B Wittwer, Thorsten Neef, Klaus Wippermann, Jens Wahlers, Thorsten J Cardiothorac Surg Research Article OBJECTIVE: The aim of this prospective observational study was to evaluate the efficiency of a new escalating treatment strategy with vernakalant, flecainide and electrical cardioversion (EC) in patients with new onset atrial fibrillation (AF) after cardiac surgery. MATERIAL AND METHODS: 24 patients with new onset AF after aortic valve surgery, coronary artery bypass surgery or combined procedures were evaluated in this study. Additional including criteria were age between 18 and 80, duration of AF less than four days, body weight less than 100 kg and no previous treatment with class I or III antiarrhythmic drugs. Exclusion criteria were poor left ventricular ejection fraction (LVEF < 40%) and history of myocardial infarction within 30 days. The patients were divided into converters and non-converters according to their response to combination treatment with vernakalant and flecainide, and the groups were compared. RESULTS: The mean age of the population was 69.6 ± 6.3 years and 26.1% of patients were female. There were no statistically significant differences between the two groups in terms of height, weight, gender distribution, comorbidities, preoperative medication, left ventricular function and left atrium diameter. Interventricular septum (IVS) in the non-converted group was significantly thicker compared to the converted group: 14.0 ± 1.00 vs. 10.40 ± 2.59 mm (p = 0.036). While 14 patients (60.9%) were successfully converted into stable sinus rhythm by pharmacological treatment with vernakalant and flecainide, 9 patients (39.1%, non-converted group) remained in AF. However, seven of them could be converted after additional EC. CONCLUSION: The combination of vernakalant and flecainide improves the conversion rate into a stable sinus rhythm in postcardiotomy patients with new onset AF compared to single drug therapy. Furthermore it might be an excellent precondition for successful EC in patients who are not converted after using both antiarrhtythmic drugs. Furthermore, left ventricular hypertrophy might be a potential negative predictor of successful pharmacological cardioversion. BioMed Central 2014-05-12 /pmc/articles/PMC4045875/ /pubmed/24886207 http://dx.doi.org/10.1186/1749-8090-9-83 Text en Copyright © 2014 Zeriouh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zeriouh, Mohamed Sabashnikov, Anton Choi, Yeong-Hoon Fatullayev, Javid Reuter, Hannes Popov, Aron-Frederik Langebartels, Georg Kimmig, Lucas Rahmanian, Parwis B Wittwer, Thorsten Neef, Klaus Wippermann, Jens Wahlers, Thorsten A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
title | A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
title_full | A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
title_fullStr | A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
title_full_unstemmed | A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
title_short | A novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
title_sort | novel treatment strategy of new onset atrial fibrillation after cardiac surgery: an observational prospective study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045875/ https://www.ncbi.nlm.nih.gov/pubmed/24886207 http://dx.doi.org/10.1186/1749-8090-9-83 |
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