Risk of Stroke or Systemic Embolism According to Baseline Frequency and Duration of Subclinical Atrial Fibrillation: Insights From the ARTESiA Trial.

anticoagulants atrial fibrillation defibrillators stroke

Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
04 Sep 2024
Historique:
medline: 4 9 2024
pubmed: 4 9 2024
entrez: 4 9 2024
Statut: aheadofprint

Résumé

In the ARTESiA trial (Apixaban for the Reduction of Thromboembolism in Patients With Device-Detected Subclinical Atrial Fibrillation), apixaban, compared with aspirin, reduced stroke or systemic embolism in patients with device-detected subclinical atrial fibrillation (SCAF). Clinical guidelines recommend considering SCAF episode duration when deciding whether to prescribe oral anticoagulation for this population. We performed a retrospective cohort study in ARTESiA. Using Cox regression adjusted for CHA Among 3986 patients with complete baseline SCAF data, 703 (17.6%) had no SCAF episode ≥6 minutes in the 6 months before enrollment. Among 3283 patients (82.4%) with ≥1 episode of SCAF ≥6 minutes in the 6 months before enrollment, 2542 (77.4%) had up to 5 episodes, and 741 (22.6%) had ≥6 episodes. The longest episode lasted <1 hour in 1030 patients (31.4%), 1 to <6 hours in 1421 patients (43.3%), and >6 hours in 832 patients (25.3%). Higher baseline SCAF frequency was not associated with increased risk of stroke or systemic embolism: 1.1% for 1 to 5 episodes versus 1.2%/patient-year for ≥6 episodes (adjusted hazard ratio, 0.89 [95% CI, 0.59-1.34]). In an exploratory analysis, patients with previous SCAF but no episode ≥6 minutes in the 6 months before enrollment had a lower risk of stroke or systemic embolism than patients with at least one episode during that period (0.5% versus 1.1%/patient-year; adjusted hazard ratio, 0.48 [95% CI, 0.27-0.85]). The frequency of SCAF did not modify the reduction in stroke or systemic embolism with apixaban ( In ARTESiA, baseline SCAF frequency and longest episode duration were not associated with risk of stroke or systemic embolism and did not modify the effect of apixaban on reduction of stroke or systemic embolism. URL: https://www.clinicaltrials.gov; Unique identifier: NCT01938248.

Sections du résumé

BACKGROUND UNASSIGNED
In the ARTESiA trial (Apixaban for the Reduction of Thromboembolism in Patients With Device-Detected Subclinical Atrial Fibrillation), apixaban, compared with aspirin, reduced stroke or systemic embolism in patients with device-detected subclinical atrial fibrillation (SCAF). Clinical guidelines recommend considering SCAF episode duration when deciding whether to prescribe oral anticoagulation for this population.
METHODS UNASSIGNED
We performed a retrospective cohort study in ARTESiA. Using Cox regression adjusted for CHA
RESULTS UNASSIGNED
Among 3986 patients with complete baseline SCAF data, 703 (17.6%) had no SCAF episode ≥6 minutes in the 6 months before enrollment. Among 3283 patients (82.4%) with ≥1 episode of SCAF ≥6 minutes in the 6 months before enrollment, 2542 (77.4%) had up to 5 episodes, and 741 (22.6%) had ≥6 episodes. The longest episode lasted <1 hour in 1030 patients (31.4%), 1 to <6 hours in 1421 patients (43.3%), and >6 hours in 832 patients (25.3%). Higher baseline SCAF frequency was not associated with increased risk of stroke or systemic embolism: 1.1% for 1 to 5 episodes versus 1.2%/patient-year for ≥6 episodes (adjusted hazard ratio, 0.89 [95% CI, 0.59-1.34]). In an exploratory analysis, patients with previous SCAF but no episode ≥6 minutes in the 6 months before enrollment had a lower risk of stroke or systemic embolism than patients with at least one episode during that period (0.5% versus 1.1%/patient-year; adjusted hazard ratio, 0.48 [95% CI, 0.27-0.85]). The frequency of SCAF did not modify the reduction in stroke or systemic embolism with apixaban (
CONCLUSIONS UNASSIGNED
In ARTESiA, baseline SCAF frequency and longest episode duration were not associated with risk of stroke or systemic embolism and did not modify the effect of apixaban on reduction of stroke or systemic embolism.
REGISTRATION UNASSIGNED
URL: https://www.clinicaltrials.gov; Unique identifier: NCT01938248.

Identifiants

pubmed: 39229707
doi: 10.1161/CIRCULATIONAHA.124.069903
doi:

Banques de données

ClinicalTrials.gov
['NCT01938248']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

William F McIntyre (WF)

Population Health Research Institute, Hamilton, Canada. (W.M., S.F.L.).

Alexander P Benz (AP)

McMaster University (A.B., J.H., S.C.), Hamilton, Canada.

Jeff S Healey (JS)

McMaster University (A.B., J.H., S.C.), Hamilton, Canada.

Stuart J Connolly (SJ)

McMaster University (A.B., J.H., S.C.), Hamilton, Canada.

Mu Yang (M)

University of Waterloo, Canada (M.Y.).

Shun Fu Lee (SF)

Population Health Research Institute, Hamilton, Canada. (W.M., S.F.L.).

Thalia S Field (TS)

Vancouver Stroke Program, University of British Columbia, Canada (T.F.).

Marco Alings (M)

Working Group on Cardiovascular Research (M.A.).

J Benezet-Mazuecos (J)

Hospital Universitario La Luz, Madrid, Spain (J.B.-M.).

Giuseppe Boriani (G)

University of Modena and Reggio Emilia, Modena, Italy (G.B.).

J Cosedis Nielsen (JC)

Aarhus University Hospital, Denmark (J.N.).

Michael R Gold (MR)

Medical University of South Carolina, Charleston (M.G.).

Francesco Pergolini (F)

Maggiore Hospital, Bologna, Italy (F.P.).

Taya V Glotzer (TV)

Hackensack University Medical Center, NJ (T.G.).

Christopher B Granger (CB)

Duke University (C.G.), Durham, NC.

Renato D Lopes (RD)

Duke Clinical Research Institute (R.L.).

Classifications MeSH