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Antithrombotic therapies in Canadian atrial fibrillation patients with concomitant coronary artery disease: Insights from the CONNECT AF + PCI-II program.
Chow, James K; Bagai, Akshay; Tan, Mary K; Har, Bryan J; Yip, Amelia M C; Paniagua, Mario; Elbarouni, Basem; Bainey, Kevin R; Paradis, Jean-Michel; Maranda, Robert; Cantor, Warren J; Eisenberg, Mark J; Dery, Jean-Pierre; Madan, Mina; Cieza, Tomas; Matteau, Alexis; Roth, Sherryn; Lavi, Shahar; Glanz, Anthony; Gao, Dongsheng; Tahiliani, Ravi; Welsh, Robert C; Kim, Hahn Hoe; Robinson, Simon D; Daneault, Benoit; Chong, Aun-Yeong; Le May, Michel R; Ahooja, Vineeta; Gregoire, Jean C; Nadeau, Pierre-Louis; Laksman, Zachary; Heilbron, Brett; Yung, Derek; Minhas, Kunal; Bourgeois, Ronald; Overgaard, Christopher B; Bonakdar, Hamid; Logsetty, Giridhar; Lavoie, Andrea J; De LaRochelliere, Robert; Mansour, Samer; Spindler, Caroline; Yan, Andrew T; Goodman, Shaun G.
Afiliación
  • Chow JK; University of Edinburgh, Edinburgh, UK.
  • Bagai A; University of Toronto, Toronto, Canada; St Michael's Hospital, Toronto, Canada.
  • Tan MK; Canadian Heart Research Centre, Toronto, Canada.
  • Har BJ; Libin Cardiovascular Institute, University of Calgary, Calgary, Canada.
  • Yip AMC; St. Mary's General Hospital, Kitchener-Waterloo, Canada.
  • Paniagua M; Hôpital Pierre de Sorel, Sorel-Tracy, Quebec, Canada.
  • Elbarouni B; St Boniface Hospital, University of Manitoba, Winnipeg, Canada.
  • Bainey KR; Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Canada.
  • Paradis JM; Institut universitaire de cardiologie et de pneumologie de Québec, Laval University, Quebec, Canada.
  • Maranda R; Ottawa Cardiovascular Centre, Ottawa, Canada.
  • Cantor WJ; University of Toronto, Toronto, Canada; Southlake Regional Health Centre, Newmarket, Canada.
  • Eisenberg MJ; Jewish General Hospital, McGill University, Montreal, Canada.
  • Dery JP; Institut universitaire de cardiologie et de pneumologie de Québec, Laval University, Quebec, Canada.
  • Madan M; University of Toronto, Toronto, Canada; Schulich Heart Centre, Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Cieza T; Institut universitaire de cardiologie et de pneumologie de Québec, Laval University, Quebec, Canada.
  • Matteau A; Centre hospitalier de l'université de Montréal (CHUM), Montreal, Canada.
  • Roth S; Schulich Heart Centre, Sunnybrook Health Sciences Centre, Toronto, Canada; Scarborough Health Network, Toronto, Canada.
  • Lavi S; Western University, London, Canada.
  • Glanz A; Windsor Regional Hospital, Windsor, Canada.
  • Gao D; Cape Breton Regional Hospital, Sydney, Canada.
  • Tahiliani R; Central East Regional Cardiac Care Program, Oshawa, Canada.
  • Welsh RC; Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Canada.
  • Kim HH; St. Mary's General Hospital, Kitchener-Waterloo, Canada.
  • Robinson SD; Royal Jubilee Hospital, University of British Columbia, Victoria, Canada.
  • Daneault B; Centre hospitalier Universitaire de Sherbrooke, Sherbrooke University, Sherbrooke, Canada.
  • Chong AY; University of Ottawa Heart Institute, Ottawa, Canada.
  • Le May MR; University of Ottawa Heart Institute, Ottawa, Canada.
  • Ahooja V; Heart Health Institute, Toronto, Canada.
  • Gregoire JC; Institut de Cardiologie de Montreal, Montreal, Canada.
  • Nadeau PL; Centre Hospitalier Universitaire de Québec, Quebec, Canada.
  • Laksman Z; University of British Columbia, Vancouver, Canada.
  • Heilbron B; University of British Columbia, Vancouver, Canada; St. Paul's Hospital, Vancouver, Canada.
  • Yung D; Scarborough Health Network, Toronto, Canada.
  • Minhas K; St Boniface Hospital, University of Manitoba, Winnipeg, Canada.
  • Bourgeois R; Moncton Hospital, Dalhousie University Faculty of Medicine, Moncton, Canada.
  • Overgaard CB; Southlake Regional Health Centre, Newmarket, Canada.
  • Bonakdar H; St Boniface Hospital, University of Manitoba, Winnipeg, Canada.
  • Logsetty G; St. Joseph's Health Centre, University of Toronto, Toronto, Canada.
  • Lavoie AJ; Regina General Hospital - Prairie Vascular Research Network, Regina, Canada.
  • De LaRochelliere R; Institut universitaire de cardiologie et de pneumologie de Québec, Laval University, Quebec, Canada.
  • Mansour S; Centre hospitalier de l'université de Montréal (CHUM), Montreal, Canada.
  • Spindler C; Canadian Heart Research Centre, Toronto, Canada.
  • Yan AT; University of Toronto, Toronto, Canada; St Michael's Hospital, Toronto, Canada. Electronic address: Andrew.yan@unityhealth.to.
  • Goodman SG; University of Toronto, Toronto, Canada; St Michael's Hospital, Toronto, Canada; Canadian Heart Research Centre, Toronto, Canada. Electronic address: goodmans@chrc.net.
J Cardiol ; 82(2): 153-161, 2023 08.
Article en En | MEDLINE | ID: mdl-36931433
ABSTRACT

BACKGROUND:

Selecting the appropriate antithrombotic regimen for patients with atrial fibrillation (AF) who have undergone percutaneous coronary intervention (PCI) or have had medically managed acute coronary syndrome (ACS) remains complex. This multi-centre observational study evaluated patterns of antithrombotic therapies utilized among Canadian patients with AF post-PCI or ACS. METHODS AND

RESULTS:

By retrospective chart audit, 611 non-valvular AF patients [median (interquartile range) age 76 (69-83) years, CHADS2 score 2 (1-3)] who underwent PCI or had medically managed ACS between August 2018 and December 2020 were identified by 68 cardiologists across eight provinces in Canada. Overall, triple antithrombotic therapy [TAT combined oral anticoagulation (OAC) and dual antiplatelet therapy (DAPT)] was the most common initial antithrombotic strategy, with use in 53.8 % of patients, followed by dual pathway therapy (32.7 % received OAC and a P2Y12 inhibitor, and 4.1 % received OAC and aspirin) and DAPT (9.3 %). Median duration of TAT was 30 (7, 30) days. Compared to the previous CONNECT AF + PCI-I program, there was an increased use of dual pathway therapy relative to TAT over time (P-value <.0001). DOACs (direct oral anticoagulants) represented 90.3 % of all OACs used overall, with apixaban being the most utilized (50.5 %). Proton pump inhibitors were used in 57.0 % of all patients, and 70.1 % of patients on ASA. Planned antithrombotic therapies at 1 year were 76.2 % OAC monotherapy, 8.3 % OAC + ASA, 7.9 % OAC + P2Y12 inhibitor, 4.3 % DAPT, 1.3 % ASA alone, and <1 % triple therapy.

CONCLUSION:

In accordance with recent Canadian Cardiovascular Society guideline recommendations, we observed an increased use of dual pathway therapy relative to TAT over time in both AF patients post-PCI (elective and emergent) and in those with medically managed ACS. Additionally, DOACs have become the prevailing form of anticoagulation across all antithrombotic regimens. Our findings suggest that Canadian physicians are integrating evidence-based approaches to optimally manage the bleeding and thrombotic risks of AF patients post-PCI and/or ACS.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fibrilación Atrial / Enfermedad de la Arteria Coronaria / Intervención Coronaria Percutánea Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans País/Región como asunto: America do norte Idioma: En Revista: J Cardiol Asunto de la revista: CARDIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fibrilación Atrial / Enfermedad de la Arteria Coronaria / Intervención Coronaria Percutánea Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans País/Región como asunto: America do norte Idioma: En Revista: J Cardiol Asunto de la revista: CARDIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido