Left Atrial Appendage Closure Compared With Oral Anticoagulants for Patients With Atrial Fibrillation: A Systematic Review and Network Meta-Analysis.

atrial fibrillation bleeding left atrial appendage closure oral anticoagulation stroke

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
09 Aug 2024
Historique:
medline: 9 8 2024
pubmed: 9 8 2024
entrez: 9 8 2024
Statut: aheadofprint

Résumé

Percutaneous left atrial appendage closure (LAAC) has been suggested as an alternative to long-term oral anticoagulation for nonvalvular atrial fibrillation, but comparative data remain scarce. We aimed to assess ischemic and bleeding outcomes of LAAC compared with vitamin K antagonists (VKAs) or direct oral anticoagulants (DOACs) for the prevention of cardioembolic events in patients with atrial fibrillation. Embase and MEDLINE were searched for randomized trials comparing LAAC, VKAs, and DOACs. The primary efficacy end point was any stroke or systemic embolism. Treatment effects were calculated from a network meta-analysis and ranked according to the surface under the cumulative ranking curve. Seven trials and 73 199 patients were included. The risk of the primary end point was not statistically different between LAAC versus VKAs (odds ratio [OR], 0.92 [95% CI, 0.62-1.50]) and LAAC versus DOACs (OR, 1.11 [95% CI, 0.71-1.73]). LAAC and DOACs resulted in similar risk of major or minor (OR, 0.93 [95% CI, 0.61-1.42]) and major bleeding (OR, 0.92 [95% CI, 0.58-1.46]); however, after exclusion of procedural bleeding, bleeding risk was significantly lower in those undergoing LAAC. Both LAAC and DOACs reduced the risk of all-cause death  compared with VKAs (LAAC versus VKAs: OR, 0.70 [95% CI, 0.53-0.91]; DOACs versus VKAs: OR, 0.90 [95% CI, 0.85-0.95], respectively). DOACs ranked as the best treatment for stroke or systemic embolism prevention (66.9%) and LAAC for reducing major bleeding (63.9%) and death (96.4%). As a nonpharmacological alternative to oral anticoagulation for atrial fibrillation, LAAC showed similar efficacy and safety compared with VKAs or DOACs. Prospective confirmation from larger studies is warranted.

Sections du résumé

BACKGROUND BACKGROUND
Percutaneous left atrial appendage closure (LAAC) has been suggested as an alternative to long-term oral anticoagulation for nonvalvular atrial fibrillation, but comparative data remain scarce. We aimed to assess ischemic and bleeding outcomes of LAAC compared with vitamin K antagonists (VKAs) or direct oral anticoagulants (DOACs) for the prevention of cardioembolic events in patients with atrial fibrillation.
METHODS AND RESULTS RESULTS
Embase and MEDLINE were searched for randomized trials comparing LAAC, VKAs, and DOACs. The primary efficacy end point was any stroke or systemic embolism. Treatment effects were calculated from a network meta-analysis and ranked according to the surface under the cumulative ranking curve. Seven trials and 73 199 patients were included. The risk of the primary end point was not statistically different between LAAC versus VKAs (odds ratio [OR], 0.92 [95% CI, 0.62-1.50]) and LAAC versus DOACs (OR, 1.11 [95% CI, 0.71-1.73]). LAAC and DOACs resulted in similar risk of major or minor (OR, 0.93 [95% CI, 0.61-1.42]) and major bleeding (OR, 0.92 [95% CI, 0.58-1.46]); however, after exclusion of procedural bleeding, bleeding risk was significantly lower in those undergoing LAAC. Both LAAC and DOACs reduced the risk of all-cause death  compared with VKAs (LAAC versus VKAs: OR, 0.70 [95% CI, 0.53-0.91]; DOACs versus VKAs: OR, 0.90 [95% CI, 0.85-0.95], respectively). DOACs ranked as the best treatment for stroke or systemic embolism prevention (66.9%) and LAAC for reducing major bleeding (63.9%) and death (96.4%).
CONCLUSIONS CONCLUSIONS
As a nonpharmacological alternative to oral anticoagulation for atrial fibrillation, LAAC showed similar efficacy and safety compared with VKAs or DOACs. Prospective confirmation from larger studies is warranted.

Identifiants

pubmed: 39119987
doi: 10.1161/JAHA.124.034815
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e034815

Auteurs

Angelo Oliva (A)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.
Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Cardio Center Humanitas Clinical and Research Hospital IRCCS Rozzano Italy.

Anna Maria Ioppolo (AM)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.

Mauro Chiarito (M)

Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Cardio Center Humanitas Clinical and Research Hospital IRCCS Rozzano Italy.

Alberto Cremonesi (A)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.
Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.

Alessia Azzano (A)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.

Eligio Miccichè (E)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.

Andrea Mangiameli (A)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.

Francesco Ariano (F)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.

Giuseppe Ferrante (G)

Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Cardio Center Humanitas Clinical and Research Hospital IRCCS Rozzano Italy.

Bernhard Reimers (B)

Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Cardio Center Humanitas Clinical and Research Hospital IRCCS Rozzano Italy.

Philippe Garot (P)

Institut Cardiovasculaire Paris Sud (ICPS), Hôpital Privé Jacques Cartier Ramsay-Santé Massy France.

Nicolas Amabile (N)

Institut Cardiovasculaire Paris Sud (ICPS), Hôpital Privé Jacques Cartier Ramsay-Santé Massy France.

Roxana Mehran (R)

The Zena and Michael A. Wiener Cardiovascular Institute Icahn School of Medicine at Mount Sinai New York NY USA.

Gianluigi Condorelli (G)

Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Cardio Center Humanitas Clinical and Research Hospital IRCCS Rozzano Italy.

Giulio Stefanini (G)

Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Cardio Center Humanitas Clinical and Research Hospital IRCCS Rozzano Italy.

Davide Cao (D)

Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.
Department of Biomedical Sciences Humanitas University Pieve Emanuele MI Italy.
Institut Cardiovasculaire Paris Sud (ICPS), Hôpital Privé Jacques Cartier Ramsay-Santé Massy France.

Classifications MeSH