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Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials

INTRODUCTION: The phase 3 EURIDIS and ADONIS studies evaluated dronedarone for atrial fibrillation (AF)/atrial flutter (AFL) recurrence in patients with nonpermanent AF. Here we assessed whether patient characteristics and/or treatment outcomes in these studies differed based on the need for cardiov...

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Autores principales: Thind, Munveer, Crijns, Harry J., Naccarelli, Gerald V., Reiffel, James A., Corp dit Genti, Valérie, Wieloch, Mattias, Koren, Andrew, Kowey, Peter R.
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/PMC7318600/
https://www.ncbi.nlm.nih.gov/pubmed/32083368
http://dx.doi.org/10.1111/jce.14405
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author Thind, Munveer
Crijns, Harry J.
Naccarelli, Gerald V.
Reiffel, James A.
Corp dit Genti, Valérie
Wieloch, Mattias
Koren, Andrew
Kowey, Peter R.
author_facet Thind, Munveer
Crijns, Harry J.
Naccarelli, Gerald V.
Reiffel, James A.
Corp dit Genti, Valérie
Wieloch, Mattias
Koren, Andrew
Kowey, Peter R.
author_sort Thind, Munveer
collection PubMed
description INTRODUCTION: The phase 3 EURIDIS and ADONIS studies evaluated dronedarone for atrial fibrillation (AF)/atrial flutter (AFL) recurrence in patients with nonpermanent AF. Here we assessed whether patient characteristics and/or treatment outcomes in these studies differed based on the need for cardioversion before randomization. METHODS: Time to adjudicated first AF/AFL recurrence, symptomatic recurrence, cardiovascular hospitalization/death, and AF hospitalization, and safety were assessed by cardioversion status. RESULTS: Of 1237 patients randomized (2:1 dronedarone:placebo), 364 required baseline cardioversion (dronedarone 243, placebo 121). Patients requiring cardioversion had a greater prevalence of cardiovascular comorbidities and shorter times to first AF/AFL recurrence compared with those not requiring cardioversion. Dronedarone was associated with longer median time to first AF/AFL recurrence vs placebo regardless of cardioversion status (cardioversion: 50 vs 15 days, hazard ratio [HR] 0.76; 95% confidence interval [CI], 0.59‐0.97; P = .02; non‐cardioversion: 150 vs 77 days, HR 0.76; 95% CI, 0.64‐0.90; P < .01). Dronedarone was similarly associated with prolonged median time to symptomatic recurrence vs placebo in the cardioversion (347 vs 87 days, HR 0.65; 95% CI, 0.49‐0.87) and non‐cardioversion (288 vs 120 days, HR 0.74; 95% CI, 0.62‐0.90) populations. Risk of cardiovascular hospitalization/death and first AF hospitalization was lower with dronedarone vs placebo regardless of cardioversion status, but differences were not statistically significant. The safety of dronedarone was similar in both groups. CONCLUSION: Patients requiring baseline cardioversion represent a distinct population, having more underlying cardiovascular disease and experiencing a shorter time to AF/AFL recurrences. Dronedarone was associated with improved efficacy vs placebo regardless of cardioversion status.
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spelling pubmed-73186002020-06-29 Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials Thind, Munveer Crijns, Harry J. Naccarelli, Gerald V. Reiffel, James A. Corp dit Genti, Valérie Wieloch, Mattias Koren, Andrew Kowey, Peter R. J Cardiovasc Electrophysiol Original Articles INTRODUCTION: The phase 3 EURIDIS and ADONIS studies evaluated dronedarone for atrial fibrillation (AF)/atrial flutter (AFL) recurrence in patients with nonpermanent AF. Here we assessed whether patient characteristics and/or treatment outcomes in these studies differed based on the need for cardioversion before randomization. METHODS: Time to adjudicated first AF/AFL recurrence, symptomatic recurrence, cardiovascular hospitalization/death, and AF hospitalization, and safety were assessed by cardioversion status. RESULTS: Of 1237 patients randomized (2:1 dronedarone:placebo), 364 required baseline cardioversion (dronedarone 243, placebo 121). Patients requiring cardioversion had a greater prevalence of cardiovascular comorbidities and shorter times to first AF/AFL recurrence compared with those not requiring cardioversion. Dronedarone was associated with longer median time to first AF/AFL recurrence vs placebo regardless of cardioversion status (cardioversion: 50 vs 15 days, hazard ratio [HR] 0.76; 95% confidence interval [CI], 0.59‐0.97; P = .02; non‐cardioversion: 150 vs 77 days, HR 0.76; 95% CI, 0.64‐0.90; P < .01). Dronedarone was similarly associated with prolonged median time to symptomatic recurrence vs placebo in the cardioversion (347 vs 87 days, HR 0.65; 95% CI, 0.49‐0.87) and non‐cardioversion (288 vs 120 days, HR 0.74; 95% CI, 0.62‐0.90) populations. Risk of cardiovascular hospitalization/death and first AF hospitalization was lower with dronedarone vs placebo regardless of cardioversion status, but differences were not statistically significant. The safety of dronedarone was similar in both groups. CONCLUSION: Patients requiring baseline cardioversion represent a distinct population, having more underlying cardiovascular disease and experiencing a shorter time to AF/AFL recurrences. Dronedarone was associated with improved efficacy vs placebo regardless of cardioversion status. John Wiley and Sons Inc. 2020-03-05 2020-05 /pmc/articles/PMC7318600/ /pubmed/32083368 http://dx.doi.org/10.1111/jce.14405 Text en © 2020 The Authors. Journal of Cardiovascular Electrophysiology Published by Wiley Periodicals, Inc. 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
Thind, Munveer
Crijns, Harry J.
Naccarelli, Gerald V.
Reiffel, James A.
Corp dit Genti, Valérie
Wieloch, Mattias
Koren, Andrew
Kowey, Peter R.
Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials
title Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials
title_full Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials
title_fullStr Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials
title_full_unstemmed Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials
title_short Dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: A post hoc analysis of the EURIDIS and ADONIS trials
title_sort dronedarone treatment following cardioversion in patients with atrial fibrillation/flutter: a post hoc analysis of the euridis and adonis trials
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318600/
https://www.ncbi.nlm.nih.gov/pubmed/32083368
http://dx.doi.org/10.1111/jce.14405
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