Oral Anticoagulation Use and Left Atrial Appendage Occlusion in LAAOS III.

anticoagulants atrial appendage atrial fibrillation stroke

Journal

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

Informations de publication

Date de publication:
24 Oct 2023
Historique:
pubmed: 21 9 2023
medline: 21 9 2023
entrez: 21 9 2023
Statut: ppublish

Résumé

LAAOS III (Left Atrial Appendage Occlusion Study III) showed that left atrial appendage (LAA) occlusion reduces the risk of ischemic stroke or systemic embolism in patients with atrial fibrillation undergoing cardiac surgery. This article examines the effect of LAA occlusion on stroke reduction according to variation in the use of oral anticoagulant (OAC) therapy. Information regarding OAC use was collected at every follow-up visit. Adjusted proportional hazards modeling, including using landmarks of hospital discharge, 1 and 2 years after randomization, evaluated the effect of LAA occlusion on the risk of ischemic stroke or systemic embolism, according to OAC use. Adjusted proportional hazard modeling, with OAC use as a time-dependent covariate, was also performed to assess the effect of LAA occlusion, according to OAC use throughout the study. At hospital discharge, 3027 patients (63.5%) were receiving a vitamin K antagonist, and 879 (18.5%) were receiving a non-vitamin K antagonist oral anticoagulant (direct OAC), with no difference in OAC use between treatment arms. There were 2887 (60.5%) patients who received OACs at all follow-up visits, 1401 (29.4%) who received OAC at some visits, and 472 (9.9%) who never received OACs. The effect of LAA occlusion on the risk of ischemic stroke or systemic embolism was consistent after discharge across all 3 groups: hazard ratios of 0.70 (95% CI, 0.51-0.96), 0.63 (95% CI, 0.43-0.94), and 0.76 (95% CI, 0.32-1.79), respectively. An adjusted proportional hazards model with OAC use as a time-dependent covariate showed that the reduction in stroke or systemic embolism with LAA occlusion was similar whether patients were receiving OACs or not. The benefit of LAA occlusion was consistent whether patients were receiving OACs or not. LAA occlusion provides thromboembolism reduction in patients independent of OAC use.

Sections du résumé

BACKGROUND BACKGROUND
LAAOS III (Left Atrial Appendage Occlusion Study III) showed that left atrial appendage (LAA) occlusion reduces the risk of ischemic stroke or systemic embolism in patients with atrial fibrillation undergoing cardiac surgery. This article examines the effect of LAA occlusion on stroke reduction according to variation in the use of oral anticoagulant (OAC) therapy.
METHODS METHODS
Information regarding OAC use was collected at every follow-up visit. Adjusted proportional hazards modeling, including using landmarks of hospital discharge, 1 and 2 years after randomization, evaluated the effect of LAA occlusion on the risk of ischemic stroke or systemic embolism, according to OAC use. Adjusted proportional hazard modeling, with OAC use as a time-dependent covariate, was also performed to assess the effect of LAA occlusion, according to OAC use throughout the study.
RESULTS RESULTS
At hospital discharge, 3027 patients (63.5%) were receiving a vitamin K antagonist, and 879 (18.5%) were receiving a non-vitamin K antagonist oral anticoagulant (direct OAC), with no difference in OAC use between treatment arms. There were 2887 (60.5%) patients who received OACs at all follow-up visits, 1401 (29.4%) who received OAC at some visits, and 472 (9.9%) who never received OACs. The effect of LAA occlusion on the risk of ischemic stroke or systemic embolism was consistent after discharge across all 3 groups: hazard ratios of 0.70 (95% CI, 0.51-0.96), 0.63 (95% CI, 0.43-0.94), and 0.76 (95% CI, 0.32-1.79), respectively. An adjusted proportional hazards model with OAC use as a time-dependent covariate showed that the reduction in stroke or systemic embolism with LAA occlusion was similar whether patients were receiving OACs or not.
CONCLUSIONS CONCLUSIONS
The benefit of LAA occlusion was consistent whether patients were receiving OACs or not. LAA occlusion provides thromboembolism reduction in patients independent of OAC use.

Identifiants

pubmed: 37732457
doi: 10.1161/CIRCULATIONAHA.122.060315
pmc: PMC10589428
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1298-1304

Auteurs

Stuart J Connolly (SJ)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Jeff S Healey (JS)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Emilie P Belley-Cote (EP)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Kumar Balasubramanian (K)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Domenico Paparella (D)

University of Foggia, Italy (D.P.).
Santa Maria Hospital, GVM Care & Research, Bari, Italy (D.P.).

Katheryn Brady (K)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Wilko Reents (W)

Rhön-Klinikum Campus Bad Neustadt, Germany (W.R.).

Bernhard C Danner (BC)

Universitätsmedizin Göttingen, Germany (B.C.D.).

P J Devereaux (PJ)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Mukul Sharma (M)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Chinthanie Ramasundarahettige (C)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Salim Yusuf (S)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Richard P Whitlock (RP)

Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (S.J.C., J.S.H., E.P.B.-C., K. Balasubramanian, K. Brady, P.J.D., M.S., C.R., S.Y., R.P.W.).

Classifications MeSH