Colchicine for the Prevention of Recurrent Arrhythmia After Catheter Ablation of Atrial Fibrillation: Results of a Single-Center, Retrospective Study.


Journal

American journal of cardiovascular drugs : drugs, devices, and other interventions
ISSN: 1179-187X
Titre abrégé: Am J Cardiovasc Drugs
Pays: New Zealand
ID NLM: 100967755

Informations de publication

Date de publication:
Nov 2023
Historique:
accepted: 20 09 2023
medline: 6 11 2023
pubmed: 6 10 2023
entrez: 6 10 2023
Statut: ppublish

Résumé

There is evidence to suggest that colchicine reduces the risk of recurrent atrial fibrillation (AF) after catheter ablation; however, the tolerability and safety of colchicine in routine practice is unknown. Patients undergoing catheter ablation for AF who received colchicine after ablation were matched 1:1 to patients who did not by age, sex, and renal function. Recurrent AF was compared between groups categorically at 12 months and via propensity weighted Cox proportional hazards models with and without a 3-month blanking period. Overall, 180 patients (n = 90 colchicine and n = 90 matched controls) were followed for a median (Q1, Q3) of 10.3 (7.0, 12.0) months. Mean age was 65.3 ± 9.1 years, 33.9% were women, mean CHA Despite the frequent presence of drug-drug interactions, a 30-day course of colchicine is well-tolerated after AF ablation; however, we did not observe any association between colchicine and lower rates of AF recurrence or hospitalization.

Sections du résumé

BACKGROUND BACKGROUND
There is evidence to suggest that colchicine reduces the risk of recurrent atrial fibrillation (AF) after catheter ablation; however, the tolerability and safety of colchicine in routine practice is unknown.
METHODS METHODS
Patients undergoing catheter ablation for AF who received colchicine after ablation were matched 1:1 to patients who did not by age, sex, and renal function. Recurrent AF was compared between groups categorically at 12 months and via propensity weighted Cox proportional hazards models with and without a 3-month blanking period.
RESULTS RESULTS
Overall, 180 patients (n = 90 colchicine and n = 90 matched controls) were followed for a median (Q1, Q3) of 10.3 (7.0, 12.0) months. Mean age was 65.3 ± 9.1 years, 33.9% were women, mean CHA
CONCLUSION CONCLUSIONS
Despite the frequent presence of drug-drug interactions, a 30-day course of colchicine is well-tolerated after AF ablation; however, we did not observe any association between colchicine and lower rates of AF recurrence or hospitalization.

Identifiants

pubmed: 37801260
doi: 10.1007/s40256-023-00612-6
pii: 10.1007/s40256-023-00612-6
doi:

Substances chimiques

Colchicine SML2Y3J35T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

709-719

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Références

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Auteurs

Kristen Bova Campbell (KB)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA. k.campbell@duke.edu.

Stephanie Dougherty Eickman (SD)

William S. Middleton Memorial Veterans Hospital (Pharmacy), Madison, WI, USA.

Tracy Truong (T)

Duke Clinical Research Institute, Durham, NC, USA.
Duke Biostatistics, Epidemiology, and Research Design (BERD) Methods Core, Duke University Medical Center, Durham, NC, USA.

Eric Black-Maier (E)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Adam S Barnett (AS)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Allen Wang (A)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Cynthia L Green (CL)

Duke Clinical Research Institute, Durham, NC, USA.
Department of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.

James P Daubert (JP)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Robert K Lewis (RK)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Brett D Atwater (BD)

INOVA Health System (Electrophysiology), Fairfax, VA, USA.

Sana M Al-Khatib (SM)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.
Duke Clinical Research Institute, Durham, NC, USA.

Tristram D Bahnson (TD)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Kevin L Thomas (KL)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.
Duke Clinical Research Institute, Durham, NC, USA.

Kevin P Jackson (KP)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Larry R Jackson (LR)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Sean Pokorney (S)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.
Duke Clinical Research Institute, Durham, NC, USA.

Camille Frazier-Mills (C)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.

Jonathan P Piccini (JP)

Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.
Duke Clinical Research Institute, Durham, NC, USA.

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