Early Nonprocedural Bleeding After Left Atrial Appendage Occlusion.

anticoagulant atrial fibrillation bleeding left atrial appendage occlusion

Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
13 Jul 2024
Historique:
received: 19 02 2024
revised: 07 05 2024
accepted: 21 05 2024
medline: 18 7 2024
pubmed: 18 7 2024
entrez: 18 7 2024
Statut: aheadofprint

Résumé

Patients treated with left atrial appendage occlusion (LAAO) are at high bleeding risk. Intensive antithrombotic treatment is recommended after the procedure to prevent device-related thrombosis. This study sought to evaluate the incidence, consequences, and predictors of early nonprocedural bleeding after LAAO. This was a multicenter study including 1,649 patients undergoing LAAO in 9 centers. Early nonprocedural bleeding was defined as bleeding unrelated to the procedure occurring within 3 months after device implantation. The severity of bleeding was defined by the Valve Academic Research Consortium-2 classification. A sensitivity analysis was performed at 45 days. A total of 121 (7.3%) patients experienced early nonprocedural bleeding events, and 69 (57.0%) were classified as major bleeding (4.2% of patients). Independent predictors of early nonprocedural bleeding were dual antiplatelet therapy (DAPT) at discharge (adjusted HR [aHR]: 1.61; 95% CI: 1.12-2.33; P = 0.01), prior gastrointestinal bleeding (aHR: 2.15; 95% CI: 1.38-3.35; P < 0.001), and multiple locations of prior bleeding (aHR: 2.33; 95% CI: 1.34-4.05; P < 0.001). DAPT at discharge was predictive of both all and major nonprocedural bleeding at 3 months and 45 days. After a median follow-up of 2.3 years (Q1-Q3: 1.1-4.1 years), early nonprocedural bleeding was independently associated with an increased risk of all-cause death (aHR: 1.53; 95% CI: 1.15-2.06; P < 0.001). This heightened mortality risk was similar at 45 days. Early nonprocedural bleeding after LAAO occurred in ∼7% of patients within 3 months, with more than one-half being classified as major bleeding. Regardless of severity, early nonprocedural bleeding was associated with increased mortality. DAPT at discharge determined an increased risk of early nonprocedural bleeding after LAAO. These results emphasize the importance of bleeding risk for determining antithrombotic strategies after LAAO.

Sections du résumé

BACKGROUND BACKGROUND
Patients treated with left atrial appendage occlusion (LAAO) are at high bleeding risk. Intensive antithrombotic treatment is recommended after the procedure to prevent device-related thrombosis.
OBJECTIVES OBJECTIVE
This study sought to evaluate the incidence, consequences, and predictors of early nonprocedural bleeding after LAAO.
METHODS METHODS
This was a multicenter study including 1,649 patients undergoing LAAO in 9 centers. Early nonprocedural bleeding was defined as bleeding unrelated to the procedure occurring within 3 months after device implantation. The severity of bleeding was defined by the Valve Academic Research Consortium-2 classification. A sensitivity analysis was performed at 45 days.
RESULTS RESULTS
A total of 121 (7.3%) patients experienced early nonprocedural bleeding events, and 69 (57.0%) were classified as major bleeding (4.2% of patients). Independent predictors of early nonprocedural bleeding were dual antiplatelet therapy (DAPT) at discharge (adjusted HR [aHR]: 1.61; 95% CI: 1.12-2.33; P = 0.01), prior gastrointestinal bleeding (aHR: 2.15; 95% CI: 1.38-3.35; P < 0.001), and multiple locations of prior bleeding (aHR: 2.33; 95% CI: 1.34-4.05; P < 0.001). DAPT at discharge was predictive of both all and major nonprocedural bleeding at 3 months and 45 days. After a median follow-up of 2.3 years (Q1-Q3: 1.1-4.1 years), early nonprocedural bleeding was independently associated with an increased risk of all-cause death (aHR: 1.53; 95% CI: 1.15-2.06; P < 0.001). This heightened mortality risk was similar at 45 days.
CONCLUSIONS CONCLUSIONS
Early nonprocedural bleeding after LAAO occurred in ∼7% of patients within 3 months, with more than one-half being classified as major bleeding. Regardless of severity, early nonprocedural bleeding was associated with increased mortality. DAPT at discharge determined an increased risk of early nonprocedural bleeding after LAAO. These results emphasize the importance of bleeding risk for determining antithrombotic strategies after LAAO.

Identifiants

pubmed: 39023452
pii: S1936-8798(24)00814-8
doi: 10.1016/j.jcin.2024.05.032
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Cruz-González is proctor for Boston Scientific, Abbott, and Lifetech. Dr Nombela-Franco is proctor for Abbott. Dr Rodés-Cabau holds the research chair “fondation famille Jacques Larivière” for the development of structural heart interventions (Laval University), and has received institutional research grants from Boston Scientific. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Jules Mesnier (J)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Ignacio Cruz-González (I)

University Hospital of Salamanca, IBSAL, CIBER-CV, Salamanca, Spain.

Paul Guedeney (P)

Sorbonne Université, ACTION Study Group, INSERM UMRS 1166, Institut de Cardiologie (AP-HP), Paris, France.

Dabit Arzamendi (D)

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Xavier Freixa (X)

Institut Clínic Cardiovascular, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona, Spain.

Luis Nombela-Franco (L)

Cardiovascular Institute, Hospital Clínico San Carlos, Madrid, Spain.

Vicente Peral (V)

Servicio de Cardiología, Hospital Universitari Son Espases, Institut d'Investigació Sanitària Illes Balears, Palma, Balearic Islands, Spain.

Berenice Caneiro-Queija (B)

University Hospital Alvaro Cunqueiro, Vigo, Spain.

Antonio Mangieri (A)

Cardiocenter, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

Blanca Trejo-Velasco (B)

University Hospital of Salamanca, IBSAL, CIBER-CV, Salamanca, Spain.

Lluis Asmarats (L)

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Pedro Cepas-Guillén (P)

Institut Clínic Cardiovascular, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona, Spain.

Pablo Salinas (P)

Cardiovascular Institute, Hospital Clínico San Carlos, Madrid, Spain.

Joan Siquier-Padilla (J)

Servicio de Cardiología, Hospital Universitari Son Espases, Institut d'Investigació Sanitària Illes Balears, Palma, Balearic Islands, Spain.

Rodrigo Estevez-Loureiro (R)

University Hospital Alvaro Cunqueiro, Vigo, Spain.

Alessandra Laricchia (A)

GVM Care and Research, Maria Cecilia Hospital, Cotignola, Italy; ASST Fatebenefratelli Sacco, Milan, Italy.

Gilles O'Hara (G)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Gilles Montalescot (G)

Sorbonne Université, ACTION Study Group, INSERM UMRS 1166, Institut de Cardiologie (AP-HP), Paris, France.

Josep Rodés-Cabau (J)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada; Institut Clínic Cardiovascular, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona, Spain. Electronic address: josep.rodes@criucpq.ulaval.ca.

Classifications MeSH