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Left Atrial Appendage Occlusion vs Standard of Care After Ischemic Stroke Despite Anticoagulation

Authors :
Maarse, Moniek
Seiffge, David J.
Werring, David J.
Boersma, Lucas V. A.
Aarnink, Errol W.
Fierro, Nicolai
Mazzone, Patrizio
Beneduce, Alessandro
Tondo, Claudio
Gasperetti, Alessio
Pracon, Radoslaw
Demkow, Marcin
Zielinski, Kamil
de Backer, Ole
Korsholm, Kasper
Nielsen-Kudsk, Jens Erik
Estévez-Loureiro, Rodrigo
Caneiro-Queija, Berenice
Benito-González, Tomás
de Prado, Armando Pérez
Nombela-Franco, Luis
Salinas, Pablo
Holmes, David
Almakadma, Abdul H.
Berti, Sergio
Romeo, Maria Rita
Alvarez, Xavier Millan
Arzamendi, Dabit
Alla, Venkata M.
Agarwal, Himanshu
Eitel, Ingo
Paitazoglou, Christina
Freixa, Xavier
Cepas-Guillén, Pedro
Chothia, Rashaad
Badejoko, Solomon O.
Bergmann, Martin W.
Spoon, Daniel B.
Maddux, James T.
El-Chami, Mikhael
Ram, Pradhum
Branca, Luca
Adamo, Marianna
Suradi, Hussam S.
van Dijk, Vincent F.
Rensing, Benno J. W. M.
Zietz, Annaelle
Paciaroni, Maurizio
Caso, Valeria
Koga, Masatoshi
Toyoda, Kazunori
Kallmünzer, Bernd
Cappellari, Manuel
Wilson, Duncan
Engelter, Stefan
Swaans, Martin J.
Source :
JAMA Neurology; November 2024, Vol. 81 Issue: 11 p1150-1158, 9p
Publication Year :
2024

Abstract

IMPORTANCE: Patients with atrial fibrillation (AF) who have ischemic stroke despite taking oral anticoagulation therapy (OAT) have a very high risk of recurrence. Left atrial appendage occlusion (LAAO) is a mechanical stroke prevention strategy that may provide additional protection in patients with thromboembolic events under OAT. OBJECTIVE: To compare percutaneous LAAO with continuing OAT alone regarding stroke prevention in patients with AF who had a thromboembolic event despite taking OAT. DESIGN, SETTING, AND PARTICIPANTS: This cohort study was a propensity score–matched comparison of the STR-OAC LAAO cohort, an international collaboration of 21 sites combining patients from multiple prospective registries of patients who underwent LAAO between 2010 and 2022. STR-OAC LAAO cohort patients who had follow-up longer than 3 months were propensity score–matched to a previously published control cohort comprising patients from an established international collaboration of investigator-initiated prospective studies. This control cohort included patients with nonvalvular AF, recent ischemic stroke or transient ischemic attack, and follow-up longer than 3 months who were taking OAT before the index event. Analyses were adjusted for imbalances in gender, age, hypertension, diabetes, and CHA2 DS2-VASc score. EXPOSURE: Left atrial appendage occlusion vs continuation of oral anticoagulation therapy alone (control group). MAIN OUTCOMES AND MEASURES: The primary outcome was time to first ischemic stroke. RESULTS: Four hundred thirty-three patients from the STR-OAC LAAO cohort (mean [SD] age, 72 [9] years; 171 [39%] females and 262 [61%] males; mean [SD] CHA2 DS2-VASc score, 5.0 [1.6]) were matched to 433 of 1140 patients (38%) from the control group. During 2-year follow-up, 50 patients experienced ischemic stroke: an annualized event rate of 2.8% per patient-year in the STR-OAC LAAO group vs 8.9% per patient-year in the control group. Left atrial appendage occlusion was associated with a lower risk of ischemic stroke (hazard ratio, 0.33; 95% CI, 0.19-0.58; P < .001) compared with the control group. After LAAO, OAT was discontinued in 290 patients (67%), and the remaining 143 patients (33%) continued OAT after LAAO as an adjunctive therapy. CONCLUSIONS AND RELEVANCE: In patients with nonvalvular AF and a prior thromboembolic event despite taking OAT, LAAO was associated with a lower risk of ischemic stroke compared with continued OAT alone. Randomized clinical trial data are needed to confirm that LAAO may be a promising treatment option for this population with a very high risk of stroke.

Details

Language :
English
ISSN :
21686149 and 21686157
Volume :
81
Issue :
11
Database :
Supplemental Index
Journal :
JAMA Neurology
Publication Type :
Periodical
Accession number :
ejs67960709
Full Text :
https://doi.org/10.1001/jamaneurol.2024.2882