Your browser doesn't support javascript.
loading
Late Bleeding Events in Patients Undergoing Percutaneous Coronary Intervention in the Workup Pre-TAVR.
Avvedimento, Marisa; Campelo-Parada, Francisco; Munoz-Garcia, Erika; Nombela-Franco, Luis; Fischer, Quentin; Donaint, Pierre; Serra, Vicenç; Veiga, Gabriela; Gutiérrez, Enrique; Esposito, Giovanni; Vilalta, Victoria; Alperi, Alberto; Regueiro, Ander; Asmarats, Lluis; Ribeiro, Henrique B; Matta, Anthony; Munoz-Garcia, Antonio; Tirado-Conte, Gabriela; Urena, Marina; Metz, Damien; Rodenas-Alesina, Eduard; de la Torre Hernandez, Jose Maria; Fernandez-Nofrerias, Eduard; Pascual, Isaac; Vidal-Cales, Pablo; Arzamendi, Dabit; Campanha-Borges, Diego Carter; Trinh, Kim Hoang; Côté, Mélanie; Faroux, Laurent; Rodés-Cabau, Josep.
Afiliación
  • Avvedimento M; Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.
  • Campelo-Parada F; Cardiology Department, Hôpital Rangueil, CHU Toulouse, Toulouse, France.
  • Munoz-Garcia E; Cardiology Department, Hospital Universitario Virgen de la Victoria, Málaga, CIBERCV, Spain.
  • Nombela-Franco L; Cardiology Department, Instituto Cardiovascular, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico de San Carlos, Madrid, Spain.
  • Fischer Q; Cardiology Department, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Donaint P; Cardiology Department, Reims University Hospital, Reims, France.
  • Serra V; Cardiology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Veiga G; Cardiology Department, Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.
  • Gutiérrez E; Cardiology Department, Hospital Gregorio Marañon, Madrid, Spain.
  • Esposito G; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.
  • Vilalta V; Cardiology Department, Hospital Germans Trias i Pujol, Badalona, Spain.
  • Alperi A; Cardiology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Regueiro A; Cardiology Department, Institut Clínic Cardiovascular, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona, Spain.
  • Asmarats L; Cardiology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
  • Ribeiro HB; Cardiology Department, Heart Institute, University of São Paulo, São Paulo, Brazil.
  • Matta A; Cardiology Department, Hôpital Rangueil, CHU Toulouse, Toulouse, France.
  • Munoz-Garcia A; Cardiology Department, Hospital Universitario Virgen de la Victoria, Málaga, CIBERCV, Spain.
  • Tirado-Conte G; Cardiology Department, Instituto Cardiovascular, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico de San Carlos, Madrid, Spain.
  • Urena M; Cardiology Department, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Metz D; Cardiology Department, Reims University Hospital, Reims, France.
  • Rodenas-Alesina E; Cardiology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • de la Torre Hernandez JM; Cardiology Department, Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.
  • Fernandez-Nofrerias E; Cardiology Department, Hospital Germans Trias i Pujol, Badalona, Spain.
  • Pascual I; Cardiology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Vidal-Cales P; Cardiology Department, Institut Clínic Cardiovascular, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona, Spain.
  • Arzamendi D; Cardiology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
  • Campanha-Borges DC; Cardiology Department, Heart Institute, University of São Paulo, São Paulo, Brazil.
  • Trinh KH; Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.
  • Côté M; Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.
  • Faroux L; Cardiology Department, Reims University Hospital, Reims, France.
  • 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.
JACC Cardiovasc Interv ; 16(17): 2153-2164, 2023 09 11.
Article en En | MEDLINE | ID: mdl-37704301
ABSTRACT

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.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Intervención Coronaria Percutánea / Reemplazo de la Válvula Aórtica Transcatéter Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: JACC Cardiovasc Interv Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Intervención Coronaria Percutánea / Reemplazo de la Válvula Aórtica Transcatéter Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: JACC Cardiovasc Interv Asunto de la revista: ANGIOLOGIA / CARDIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Canadá