Ablation Versus Drug Therapy for Atrial Fibrillation in Heart Failure: Results From the CABANA Trial.
dc.contributor.author | Packer, Douglas L | |
dc.contributor.author | Piccini, Jonathan P | |
dc.contributor.author | Monahan, Kristi H | |
dc.contributor.author | Al-Khalidi, Hussein R | |
dc.contributor.author | Silverstein, Adam P | |
dc.contributor.author | Noseworthy, Peter A | |
dc.contributor.author | Poole, Jeanne E | |
dc.contributor.author | Bahnson, Tristram D | |
dc.contributor.author | Lee, Kerry L | |
dc.contributor.author | Mark, Daniel B | |
dc.contributor.author | CABANA Investigators | |
dc.date.accessioned | 2024-06-06T14:53:17Z | |
dc.date.available | 2024-06-06T14:53:17Z | |
dc.date.issued | 2021-04 | |
dc.description.abstract | BackgroundIn patients with heart failure and atrial fibrillation (AF), several clinical trials have reported improved outcomes, including freedom from AF recurrence, quality of life, and survival, with catheter ablation. This article describes the treatment-related outcomes of the AF patients with heart failure enrolled in the CABANA trial (Catheter Ablation Versus Antiarrhythmic Drug Therapy for Atrial Fibrillation).MethodsThe CABANA trial randomized 2204 patients with AF who were ≥65 years old or <65 years old with ≥1 risk factor for stroke at 126 sites to ablation with pulmonary vein isolation or drug therapy including rate or rhythm control drugs. Of these, 778 (35%) had New York Heart Association class >II at baseline and form the subject of this article. The CABANA trial's primary end point was a composite of death, disabling stroke, serious bleeding, or cardiac arrest.ResultsOf the 778 patients with heart failure enrolled in CABANA, 378 were assigned to ablation and 400 to drug therapy. Ejection fraction at baseline was available for 571 patients (73.0%), and 9.3% of these had an ejection fraction <40%, whereas 11.7% had ejection fractions between 40% and 50%. In the intention-to-treat analysis, the ablation arm had a 36% relative reduction in the primary composite end point (hazard ratio, 0.64 [95% CI, 0.41-0.99]) and a 43% relative reduction in all-cause mortality (hazard ratio, 0.57 [95% CI, 0.33-0.96]) compared with drug therapy alone over a median follow-up of 48.5 months. AF recurrence was decreased with ablation (hazard ratio, 0.56 [95% CI, 0.42-0.74]). The adjusted mean difference for the AFEQT (Atrial Fibrillation Effect on Quality of Life) summary score averaged over the entire 60-month follow-up was 5.0 points, favoring the ablation arm (95% CI, 2.5-7.4 points), and the MAFSI (Mayo Atrial Fibrillation-Specific Symptom Inventory) frequency score difference was -2.0 points, favoring ablation (95% CI, -2.9 to -1.2).ConclusionsIn patients with AF enrolled in the CABANA trial who had clinically diagnosed stable heart failure at trial entry, catheter ablation produced clinically important improvements in survival, freedom from AF recurrence, and quality of life relative to drug therapy. These results, obtained in a cohort most of whom had preserved left ventricular function, require independent trial verification. Registration: URL: https://www.clinicaltrials.gov/ct2/show/NCT00911508; Unique identifier: NCT0091150. | |
dc.identifier.issn | 0009-7322 | |
dc.identifier.issn | 1524-4539 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Ovid Technologies (Wolters Kluwer Health) | |
dc.relation.ispartof | Circulation | |
dc.relation.isversionof | 10.1161/circulationaha.120.050991 | |
dc.rights.uri | ||
dc.subject | CABANA Investigators | |
dc.subject | Humans | |
dc.subject | Atrial Fibrillation | |
dc.subject | Treatment Outcome | |
dc.subject | Aged | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Clinical Trials as Topic | |
dc.subject | Heart Failure | |
dc.subject | Ablation Techniques | |
dc.title | Ablation Versus Drug Therapy for Atrial Fibrillation in Heart Failure: Results From the CABANA Trial. | |
dc.type | Journal article | |
duke.contributor.orcid | Piccini, Jonathan P|0000-0003-0772-2404 | |
duke.contributor.orcid | Al-Khalidi, Hussein R|0000-0003-1375-0487 | |
duke.contributor.orcid | Silverstein, Adam P|0000-0003-2013-5087 | |
duke.contributor.orcid | Bahnson, Tristram D|0000-0001-9001-506X | |
duke.contributor.orcid | Mark, Daniel B|0000-0001-6340-8087 | |
pubs.begin-page | 1377 | |
pubs.end-page | 1390 | |
pubs.issue | 14 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Staff | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Biostatistics & Bioinformatics | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Cardiology | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.organisational-group | Population Health Sciences | |
pubs.organisational-group | Biostatistics & Bioinformatics, Division of Biostatistics | |
pubs.publication-status | Published | |
pubs.volume | 143 |
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