Late Bleeding Events in Patients Undergoing Percutaneous Coronary Intervention in the Workup Pre-TAVR.


Journal

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

Informations de publication

Date de publication:
11 09 2023
Historique:
received: 23 04 2023
revised: 20 06 2023
accepted: 27 06 2023
medline: 15 9 2023
pubmed: 14 9 2023
entrez: 13 9 2023
Statut: ppublish

Résumé

In patients undergoing percutaneous coronary intervention (PCI) in the work-up pre-transcatheter aortic valve replacement (TAVR), the incidence and clinical impact of late bleeding events (LBEs) remain largely unknown. This study sought to determine the incidence, clinical characteristics, associated factors, and outcomes of LBEs in patients undergoing PCI in the work-up pre-TAVR. This was a multicenter study including 1,457 consecutive patients (mean age 81 ± 7 years; 41.5% women) who underwent TAVR and survived beyond 30 days. LBEs (>30 days post-TAVR) were defined according to the Valve Academic Research Consortium-2 criteria. LBEs occurred in 116 (7.9%) patients after a median follow-up of 23 (IQR: 12-40) months. Late bleeding was minor, major, and life-threatening or disabling in 21 (18.1%), 63 (54.3%), and 32 (27.6%) patients, respectively. Periprocedural (<30 days post-TAVR) major bleeding and the combination of antiplatelet and anticoagulation therapy at discharge were independent factors associated with LBEs (P ≤ 0.02 for all). LBEs conveyed an increased mortality risk at 4-year follow-up compared with no bleeding (43.9% vs 36.0; P = 0.034). Also, LBE was identified as an independent predictor of all-cause mortality after TAVR (HR: 1.39; 95% CI: 1.05-1.83; P = 0.020). In TAVR candidates with concomitant significant coronary artery disease requiring percutaneous treatment, LBEs after TAVR were frequent and associated with increased mortality. Combining antiplatelet and anticoagulation regimens and the occurrence of periprocedural bleeding determined an increased risk of LBEs. Preventive strategies should be pursued for preventing late bleeding after TAVR, and further studies are needed to provide more solid evidence on the most safe and effective antithrombotic regimen post-TAVR in this challenging group of patients.

Sections du résumé

BACKGROUND
In patients undergoing percutaneous coronary intervention (PCI) in the work-up pre-transcatheter aortic valve replacement (TAVR), the incidence and clinical impact of late bleeding events (LBEs) remain largely unknown.
OBJECTIVES
This study sought to determine the incidence, clinical characteristics, associated factors, and outcomes of LBEs in patients undergoing PCI in the work-up pre-TAVR.
METHODS
This was a multicenter study including 1,457 consecutive patients (mean age 81 ± 7 years; 41.5% women) who underwent TAVR and survived beyond 30 days. LBEs (>30 days post-TAVR) were defined according to the Valve Academic Research Consortium-2 criteria.
RESULTS
LBEs occurred in 116 (7.9%) patients after a median follow-up of 23 (IQR: 12-40) months. Late bleeding was minor, major, and life-threatening or disabling in 21 (18.1%), 63 (54.3%), and 32 (27.6%) patients, respectively. Periprocedural (<30 days post-TAVR) major bleeding and the combination of antiplatelet and anticoagulation therapy at discharge were independent factors associated with LBEs (P ≤ 0.02 for all). LBEs conveyed an increased mortality risk at 4-year follow-up compared with no bleeding (43.9% vs 36.0; P = 0.034). Also, LBE was identified as an independent predictor of all-cause mortality after TAVR (HR: 1.39; 95% CI: 1.05-1.83; P = 0.020).
CONCLUSIONS
In TAVR candidates with concomitant significant coronary artery disease requiring percutaneous treatment, LBEs after TAVR were frequent and associated with increased mortality. Combining antiplatelet and anticoagulation regimens and the occurrence of periprocedural bleeding determined an increased risk of LBEs. Preventive strategies should be pursued for preventing late bleeding after TAVR, and further studies are needed to provide more solid evidence on the most safe and effective antithrombotic regimen post-TAVR in this challenging group of patients.

Identifiants

pubmed: 37704301
pii: S1936-8798(23)01034-8
doi: 10.1016/j.jcin.2023.06.037
pii:
doi:

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2153-2164

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Rodés-Cabau holds the Research Chair “Fondation Famille Jacques Larivière” for the Development of Structural Heart Disease Interventions (Laval University); and has received institutional research grants and speaker/consultant fees from Edwards Lifesciences and Medtronic. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Marisa Avvedimento (M)

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

Francisco Campelo-Parada (F)

Cardiology Department, Hôpital Rangueil, CHU Toulouse, Toulouse, France.

Erika Munoz-Garcia (E)

Cardiology Department, Hospital Universitario Virgen de la Victoria, Málaga, CIBERCV, Spain.

Luis Nombela-Franco (L)

Cardiology Department, Instituto Cardiovascular, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico de San Carlos, Madrid, Spain.

Quentin Fischer (Q)

Cardiology Department, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Pierre Donaint (P)

Cardiology Department, Reims University Hospital, Reims, France.

Vicenç Serra (V)

Cardiology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Gabriela Veiga (G)

Cardiology Department, Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.

Enrique Gutiérrez (E)

Cardiology Department, Hospital Gregorio Marañon, Madrid, Spain.

Giovanni Esposito (G)

Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Victoria Vilalta (V)

Cardiology Department, Hospital Germans Trias i Pujol, Badalona, Spain.

Alberto Alperi (A)

Cardiology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.

Ander Regueiro (A)

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

Lluis Asmarats (L)

Cardiology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.

Henrique B Ribeiro (HB)

Cardiology Department, Heart Institute, University of São Paulo, São Paulo, Brazil.

Anthony Matta (A)

Cardiology Department, Hôpital Rangueil, CHU Toulouse, Toulouse, France.

Antonio Munoz-Garcia (A)

Cardiology Department, Hospital Universitario Virgen de la Victoria, Málaga, CIBERCV, Spain.

Gabriela Tirado-Conte (G)

Cardiology Department, Instituto Cardiovascular, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico de San Carlos, Madrid, Spain.

Marina Urena (M)

Cardiology Department, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Damien Metz (D)

Cardiology Department, Reims University Hospital, Reims, France.

Eduard Rodenas-Alesina (E)

Cardiology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Jose Maria de la Torre Hernandez (JM)

Cardiology Department, Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.

Eduard Fernandez-Nofrerias (E)

Cardiology Department, Hospital Germans Trias i Pujol, Badalona, Spain.

Isaac Pascual (I)

Cardiology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.

Pablo Vidal-Cales (P)

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

Dabit Arzamendi (D)

Cardiology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.

Diego Carter Campanha-Borges (DC)

Cardiology Department, Heart Institute, University of São Paulo, São Paulo, Brazil.

Kim Hoang Trinh (KH)

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

Mélanie Côté (M)

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

Laurent Faroux (L)

Cardiology Department, Reims University Hospital, Reims, France.

Josep Rodés-Cabau (J)

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

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Classifications MeSH