Influence of atrial fibrillation type on outcomes of ablation vs. drug therapy: results from CABANA.

dc.contributor.author

Monahan, Kristi H

dc.contributor.author

Bunch, T Jared

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Mark, Daniel B

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Poole, Jeanne E

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Bahnson, Tristram D

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Al-Khalidi, Hussein R

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Silverstein, Adam P

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Daniels, Melanie R

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Lee, Kerry L

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Packer, Douglas L

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CABANA Investigators

dc.date.accessioned

2024-06-06T14:59:39Z

dc.date.available

2024-06-06T14:59:39Z

dc.date.issued

2022-10

dc.description.abstract

Aims

Influence of atrial fibrillation (AF) type on outcomes seen with catheter ablation vs. drug therapy is incompletely understood. This study assesses the impact of AF type on treatment outcomes in the Catheter Ablation vs. Antiarrhythmic Drug Therapy for Atrial Fibrillation Trial (CABANA).

Methods and results

CABANA randomized 2204 patients ≥65 years old or <65 with at least one risk factor for stroke to catheter ablation or drug therapy. Of these, 946 (42.9%) had paroxysmal AF (PAF), 1042 (47.3%) had persistent AF (PersAF), and 215 (9.8%) had long-standing persistent AF (LSPAF) at baseline. The primary endpoint was a composite of death, disabling stroke, serious bleeding, or cardiac arrest. Symptoms were measured with the Mayo AF-Specific Symptom Inventory (MAFSI), and quality of life was measured with the Atrial Fibrillation Effect on Quality of Life (AFEQT). Comparisons are reported by intention to treat. Compared with drug therapy alone, catheter ablation produced a 19% relative risk reduction in the primary endpoint for PAF {adjusted hazard ratio [aHR]: 0.81 [95% confidence interval (CI): 0.50, 1.30]}, and a 17% relative reduction for PersAF (aHR: 0.83, 95% CI: 0.56, 1.22). For LSPAF, the ablation relative effect was a 7% reduction (aHR: 0.93, 95% CI: 0.36, 2.44). Ablation was more effective than drug therapy at reducing first AF recurrence in all AF types: by 51% for PAF (aHR: 0.49, 95% CI: 0.39, 0.62), by 47% for PersAF (aHR: 0.53, 95% CI: 0.43,0.65), and by 36% for LSPAF (aHR 0.64, 95% CI 0.41,1.00). Ablation was associated with greater improvement in symptoms, with the mean difference between groups in the MAFSI frequency score favouring ablation over 5 years of follow-up in all subgroups: PAF had a clinically significant -1.9-point difference (95% CI: -1.2 to -2.6); PersAF a -0.9 difference (95% CI: -0.2 to -1.6); LSPAF a clinically significant difference of -1.6 points (95% CI: -0.1 to -3.1). Ablation was also associated with greater improvement in quality of life in all subgroups, with the AFEQT overall score in PAF patients showing a clinically significant 5.3-point improvement (95% CI: 3.3 to 7.3) over drug therapy alone over 5 years of follow-up, PersAF a 1.7-point difference (95% CI: 0.0 to 3.7), and LSPAF a 3.1-point difference (95% CI: -1.6 to 7.8).

Conclusion

Prognostic treatment effects of catheter ablation compared with drug therapy on the primary and major secondary clinical endpoints did not differ consequentially by AF subtype. With regard to decreases in AF recurrence and improving quality of life, ablation was more effective than drug therapy in all three AF type subgroups.

Clinicaltrials.gov identifier

NCT00911508.
dc.identifier

6595987

dc.identifier.issn

1099-5129

dc.identifier.issn

1532-2092

dc.identifier.uri

https://hdl.handle.net/10161/31131

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

dc.relation.isversionof

10.1093/europace/euac055

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

CABANA Investigators

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Humans

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Atrial Fibrillation

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Recurrence

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Anti-Arrhythmia Agents

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Catheter Ablation

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Treatment Outcome

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Quality of Life

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Aged

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Stroke

dc.title

Influence of atrial fibrillation type on outcomes of ablation vs. drug therapy: results from CABANA.

dc.type

Journal article

duke.contributor.orcid

Mark, Daniel B|0000-0001-6340-8087

duke.contributor.orcid

Bahnson, Tristram D|0000-0001-9001-506X

duke.contributor.orcid

Al-Khalidi, Hussein R|0000-0003-1375-0487

duke.contributor.orcid

Silverstein, Adam P|0000-0003-2013-5087

pubs.begin-page

1430

pubs.end-page

1440

pubs.issue

9

pubs.organisational-group

Duke

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School of Medicine

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Staff

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Biostatistics & Bioinformatics

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Medicine

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Medicine, Cardiology

pubs.organisational-group

Duke Clinical Research Institute

pubs.organisational-group

Biostatistics & Bioinformatics, Division of Biostatistics

pubs.publication-status

Published

pubs.volume

24

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