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Propafenone use in coronary artery disease patients undergoing atrial fibrillation ablation.
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- Author(s): Cay S;Cay S; Kara M; Kara M; Ozcan F; Ozcan F; Ozeke O; Ozeke O; Aksu T; Aksu T; Aras D; Aras D; Topaloglu S; Topaloglu S
- Source:
Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing [J Interv Card Electrophysiol] 2022 Nov; Vol. 65 (2), pp. 381-389. Date of Electronic Publication: 2022 Apr 02.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: Springer Country of Publication: Netherlands NLM ID: 9708966 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1572-8595 (Electronic) Linking ISSN: 1383875X NLM ISO Abbreviation: J Interv Card Electrophysiol Subsets: MEDLINE
- Publication Information: Publication: Amsterdam : Springer
Original Publication: Norwell, MA : Kluwer Academic Publishers, c1997- - Subject Terms: Atrial Fibrillation*/drug therapy ; Atrial Fibrillation*/surgery ; Coronary Artery Disease*/complications ; Coronary Artery Disease*/drug therapy ; Coronary Artery Disease*/surgery ; Amiodarone* ; Tachycardia, Ventricular*/drug therapy; Humans ; Propafenone/therapeutic use ; Retrospective Studies ; Longitudinal Studies ; Treatment Outcome ; Anti-Arrhythmia Agents/therapeutic use ; Death, Sudden, Cardiac/prevention & control
- Abstract: Background: Antiarrhythmic drugs (AADs) are frequently used after atrial fibrillation (AF) ablation. Class IC AAD use after AF ablation in patients with coronary artery disease (CAD) is uncertain. The aim was to evaluate propafenone use in CAD patients undergoing AF ablation and to compare propafenone with amiodarone regarding ventricular arrhythmia and mortality.
Methods: In this retrospective, longitudinal cohort study, consecutive patients with mild to moderate CAD, undergoing AF ablation and receiving either propafenone (study group, n = 263) or amiodarone (control group, n = 499) in the blanking period, were included. After propensity score matching, 212 patients in each group were compared for the primary outcome defined as a composite of ventricular arrhythmic events, which included sudden cardiac death, sustained ventricular tachycardia or fibrillation, or non-sustained ventricular tachycardia (NSVT). Cardiovascular and non-cardiovascular mortality were evaluated as secondary outcomes.
Results: Baseline variables of the study and control groups were well matched after propensity score matching. At 12-month follow up, 20 patients (4.7%) (11 in propafenone group and 9 in amiodarone group) experienced the primary outcome measure of NSVT (Gray test p = 0.645). No sustained ventricular tachycardia, ventricular fibrillation, sudden cardiac death, or cardiovascular mortality were observed. On multivariable competing analysis, age and diabetes but not propafenone use (hazard ratio 1.017; p = 0.804) were found to be independent and significant predictors of the primary outcome measure.
Conclusion: Propafenone use after AF ablation in patients with mild to moderate CAD had a safety profile similar to amiodarone and was not associated with major arrhythmic events.
(© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.) - Comments: Comment in: J Interv Card Electrophysiol. 2022 Nov;65(2):347-348. (PMID: 35793008)
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- Accession Number: 68IQX3T69U (Propafenone)
0 (Anti-Arrhythmia Agents)
N3RQ532IUT (Amiodarone) - Publication Date: Date Created: 20220402 Date Completed: 20221109 Latest Revision: 20221109
- Publication Date: 20231215
- Accession Number: 10.1007/s10840-022-01186-0
- Accession Number: 35366133
- Source:
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