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Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study
BACKGROUND: Antazoline mesylate represents an antihistamine capable of rapid and safe cardioversion of atrial fibrillation, yet evidence concerning its efficacy in comparison to other medications is insufficient. The study aimed to evaluate the success rate and safety of pharmacological cardioversio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474954/ https://www.ncbi.nlm.nih.gov/pubmed/30371270 http://dx.doi.org/10.1161/JAHA.118.010153 |
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author | Wybraniec, Maciej T. Wróbel, Wojciech Wilkosz, Katarzyna Wrona, Karolina Bula, Karolina Mizia‐Stec, Katarzyna |
author_facet | Wybraniec, Maciej T. Wróbel, Wojciech Wilkosz, Katarzyna Wrona, Karolina Bula, Karolina Mizia‐Stec, Katarzyna |
author_sort | Wybraniec, Maciej T. |
collection | PubMed |
description | BACKGROUND: Antazoline mesylate represents an antihistamine capable of rapid and safe cardioversion of atrial fibrillation, yet evidence concerning its efficacy in comparison to other medications is insufficient. The study aimed to evaluate the success rate and safety of pharmacological cardioversion of atrial fibrillation with intravenous antazoline (CANT [Cardioversion With Antazoline Mesylate] study) in the setting of the emergency department. METHODS AND RESULTS: After reviewing 1984 medical records, 450 eligible patients (22.7%) with short‐duration atrial fibrillation subject to pharmacological cardioversion were enrolled in a retrospective observational analysis. The choice of antiarrhythmic drug was left to the discretion of the attending physician. The primary end point was successful cardioversion in the emergency department. The safety end point comprised bradycardia <45 bpm, hypotension, syncope, or death. The study population (mean age, 65.5±11.9 years; 52.9% females) was characterized by a median atrial fibrillation episode duration of 10 hours. Antazoline, alone or in combination, was administered in 24.2% (n=109) and 40% (n=180), respectively; amiodarone was administered in 46.7% and propafenone in 9.3%, while ≥2 antiarrhythmic drugs were administered in 19.8% of patients. Antazoline had the highest success rate of pharmacological cardioversion among all drugs (85.3%), which was comparable with propafenone (78.6%; relative risk, 1.09, 95% confidence interval, 0.91–1.30; P=0.317) and higher than amiodarone treatment (66.7%; relative risk, 1.28, 95% confidence interval, 1.13–1.45; P<0.001; number needed to treat, 5.4). The rate of cardioversion with antazoline alone was higher than combined amiodarone and/or propafenone (68.1%; relative risk, 1.25; 95% confidence interval, 1.12–1.40, P=0.0001). No safety end points were reported in the antazoline group, while 5 incidents occurred in the non‐antazoline cohort (P=0.075). CONCLUSIONS: Antazoline represents an efficacious and safe method of pharmacological cardioversion in a real‐life setting. |
format | Online Article Text |
id | pubmed-6474954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64749542019-04-24 Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study Wybraniec, Maciej T. Wróbel, Wojciech Wilkosz, Katarzyna Wrona, Karolina Bula, Karolina Mizia‐Stec, Katarzyna J Am Heart Assoc Original Research BACKGROUND: Antazoline mesylate represents an antihistamine capable of rapid and safe cardioversion of atrial fibrillation, yet evidence concerning its efficacy in comparison to other medications is insufficient. The study aimed to evaluate the success rate and safety of pharmacological cardioversion of atrial fibrillation with intravenous antazoline (CANT [Cardioversion With Antazoline Mesylate] study) in the setting of the emergency department. METHODS AND RESULTS: After reviewing 1984 medical records, 450 eligible patients (22.7%) with short‐duration atrial fibrillation subject to pharmacological cardioversion were enrolled in a retrospective observational analysis. The choice of antiarrhythmic drug was left to the discretion of the attending physician. The primary end point was successful cardioversion in the emergency department. The safety end point comprised bradycardia <45 bpm, hypotension, syncope, or death. The study population (mean age, 65.5±11.9 years; 52.9% females) was characterized by a median atrial fibrillation episode duration of 10 hours. Antazoline, alone or in combination, was administered in 24.2% (n=109) and 40% (n=180), respectively; amiodarone was administered in 46.7% and propafenone in 9.3%, while ≥2 antiarrhythmic drugs were administered in 19.8% of patients. Antazoline had the highest success rate of pharmacological cardioversion among all drugs (85.3%), which was comparable with propafenone (78.6%; relative risk, 1.09, 95% confidence interval, 0.91–1.30; P=0.317) and higher than amiodarone treatment (66.7%; relative risk, 1.28, 95% confidence interval, 1.13–1.45; P<0.001; number needed to treat, 5.4). The rate of cardioversion with antazoline alone was higher than combined amiodarone and/or propafenone (68.1%; relative risk, 1.25; 95% confidence interval, 1.12–1.40, P=0.0001). No safety end points were reported in the antazoline group, while 5 incidents occurred in the non‐antazoline cohort (P=0.075). CONCLUSIONS: Antazoline represents an efficacious and safe method of pharmacological cardioversion in a real‐life setting. John Wiley and Sons Inc. 2018-10-09 /pmc/articles/PMC6474954/ /pubmed/30371270 http://dx.doi.org/10.1161/JAHA.118.010153 Text en © 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Wybraniec, Maciej T. Wróbel, Wojciech Wilkosz, Katarzyna Wrona, Karolina Bula, Karolina Mizia‐Stec, Katarzyna Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study |
title | Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study |
title_full | Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study |
title_fullStr | Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study |
title_full_unstemmed | Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study |
title_short | Pharmacological Cardioversion With Antazoline in Atrial Fibrillation: The Results of the CANT Study |
title_sort | pharmacological cardioversion with antazoline in atrial fibrillation: the results of the cant study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474954/ https://www.ncbi.nlm.nih.gov/pubmed/30371270 http://dx.doi.org/10.1161/JAHA.118.010153 |
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