Canadian Cardiovascular Society/Canadian Association of Interventional Cardiology 2023 Focused Update of the Guidelines for the Use of Antiplatelet Therapy
Antiplatelet therapy (APT) is the foundation of treatment and prevention of atherothrombotic events in patients with atherosclerotic cardiovascular disease. Selecting the optimal APT strategies to reduce major adverse cardiovascular events, while balancing bleeding risk, requires ongoing review of c...
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| Published in: | Canadian journal of cardiology Vol. 40; no. 2; pp. 160 - 181 |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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Elsevier Inc
01.02.2024
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| ISSN: | 0828-282X, 1916-7075, 1916-7075 |
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| Abstract | Antiplatelet therapy (APT) is the foundation of treatment and prevention of atherothrombotic events in patients with atherosclerotic cardiovascular disease. Selecting the optimal APT strategies to reduce major adverse cardiovascular events, while balancing bleeding risk, requires ongoing review of clinical trials. Appended, the focused update of the Canadian Cardiovascular Society/Canadian Association of Interventional Cardiology guidelines for the use of APT provides recommendations on the following topics: (1) use of acetylsalicylic acid in primary prevention of atherosclerotic cardiovascular disease; (2) dual APT (DAPT) duration after percutaneous coronary intervention (PCI) in patients at high bleeding risk; (3) potent DAPT (P2Y12 inhibitor) choice in patients who present with an acute coronary syndrome (ACS) and possible DAPT de-escalation strategies after PCI; (4) choice and duration of DAPT in ACS patients who are medically treated without revascularization; (5) pretreatment with DAPT (P2Y12 inhibitor) before elective or nonelective coronary angiography; (6) perioperative and longer-term APT management in patients who require coronary artery bypass grafting surgery; and (7) use of APT in patients with atrial fibrillation who require oral anticoagulation after PCI or medically managed ACS. These recommendations are all on the basis of systematic reviews and meta-analyses conducted as part of the development of these guidelines, provided in the Supplementary Material.
Le traitement antiplaquettaire est la base du traitement et de la prévention des manifestations athérothrombotiques chez les patients atteints d’une maladie cardiovasculaire athéroscléreuse. Le choix du traitement antiplaquettaire approprié pour réduire les événements cardiovasculaires indésirables majeurs, tout en tenant compte du risque de saignement, demande un suivi constant des essais cliniques. En annexe, la mise à jour ciblée des lignes directrices de la Société cardiovasculaire du Canada/Association canadienne de cardiologie d’intervention pour l’utilisation du traitement antiplaquettaire formule des recommandations sur les sujets suivants : 1) l’emploi de l’acide acétylsalicylique dans la prévention primaire des maladies cardiovasculaires athéroscléreuses; 2) la durée de la bithérapie antiplaquettaire après une intervention coronarienne percutanée (ICP) chez les patients qui présentent un risque élevé de saignement; 3) le choix d’une bithérapie antiplaquettaire puissante (inhibiteur de P2Y12) chez les patients qui présentent un syndrome coronarien aigu et les stratégies éventuelles de désescalade de la bithérapie antiplaquettaire après une ICP; 4) le choix et la durée de la bithérapie antiplaquettaire chez les patients atteints du syndrome coronarien aigu qui reçoivent un traitement médical sans revascularisation; 5) le prétraitement par une bithérapie antiplaquettaire (inhibiteur de P2Y12) avant une coronarographie non urgente ou urgente; 6) la prise en charge par un traitement antiplaquettaire périopératoire et à long terme chez les patients qui ont besoin d’un pontage aortocoronarien; et 7) l’utilisation du traitement antiplaquettaire chez les patients qui présentent une fibrillation auriculaire et qui ont besoin d’un traitement anticoagulant par voie orale après une ICP ou qui présentent un syndrome coronarien aigu traité médicalement. Toutes les recommandations reposent sur les analyses des publications et les méta-analyses menées dans le but de formuler ces lignes directrices, fournies dans le matériel supplémentaire. |
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| AbstractList | Antiplatelet therapy (APT) is the foundation of treatment and prevention of atherothrombotic events in patients with atherosclerotic cardiovascular disease. Selecting the optimal APT strategies to reduce major adverse cardiovascular events, while balancing bleeding risk, requires ongoing review of clinical trials. Appended, the focused update of the Canadian Cardiovascular Society/Canadian Association of Interventional Cardiology guidelines for the use of APT provides recommendations on the following topics: (1) use of acetylsalicylic acid in primary prevention of atherosclerotic cardiovascular disease; (2) dual APT (DAPT) duration after percutaneous coronary intervention (PCI) in patients at high bleeding risk; (3) potent DAPT (P2Y12 inhibitor) choice in patients who present with an acute coronary syndrome (ACS) and possible DAPT de-escalation strategies after PCI; (4) choice and duration of DAPT in ACS patients who are medically treated without revascularization; (5) pretreatment with DAPT (P2Y12 inhibitor) before elective or nonelective coronary angiography; (6) perioperative and longer-term APT management in patients who require coronary artery bypass grafting surgery; and (7) use of APT in patients with atrial fibrillation who require oral anticoagulation after PCI or medically managed ACS. These recommendations are all on the basis of systematic reviews and meta-analyses conducted as part of the development of these guidelines, provided in the Supplementary Material.
Le traitement antiplaquettaire est la base du traitement et de la prévention des manifestations athérothrombotiques chez les patients atteints d’une maladie cardiovasculaire athéroscléreuse. Le choix du traitement antiplaquettaire approprié pour réduire les événements cardiovasculaires indésirables majeurs, tout en tenant compte du risque de saignement, demande un suivi constant des essais cliniques. En annexe, la mise à jour ciblée des lignes directrices de la Société cardiovasculaire du Canada/Association canadienne de cardiologie d’intervention pour l’utilisation du traitement antiplaquettaire formule des recommandations sur les sujets suivants : 1) l’emploi de l’acide acétylsalicylique dans la prévention primaire des maladies cardiovasculaires athéroscléreuses; 2) la durée de la bithérapie antiplaquettaire après une intervention coronarienne percutanée (ICP) chez les patients qui présentent un risque élevé de saignement; 3) le choix d’une bithérapie antiplaquettaire puissante (inhibiteur de P2Y12) chez les patients qui présentent un syndrome coronarien aigu et les stratégies éventuelles de désescalade de la bithérapie antiplaquettaire après une ICP; 4) le choix et la durée de la bithérapie antiplaquettaire chez les patients atteints du syndrome coronarien aigu qui reçoivent un traitement médical sans revascularisation; 5) le prétraitement par une bithérapie antiplaquettaire (inhibiteur de P2Y12) avant une coronarographie non urgente ou urgente; 6) la prise en charge par un traitement antiplaquettaire périopératoire et à long terme chez les patients qui ont besoin d’un pontage aortocoronarien; et 7) l’utilisation du traitement antiplaquettaire chez les patients qui présentent une fibrillation auriculaire et qui ont besoin d’un traitement anticoagulant par voie orale après une ICP ou qui présentent un syndrome coronarien aigu traité médicalement. Toutes les recommandations reposent sur les analyses des publications et les méta-analyses menées dans le but de formuler ces lignes directrices, fournies dans le matériel supplémentaire. Antiplatelet therapy (APT) is the foundation of treatment and prevention of atherothrombotic events in patients with atherosclerotic cardiovascular disease. Selecting the optimal APT strategies to reduce major adverse cardiovascular events, while balancing bleeding risk, requires ongoing review of clinical trials. Appended, the focused update of the Canadian Cardiovascular Society/Canadian Association of Interventional Cardiology guidelines for the use of APT provides recommendations on the following topics: (1) use of acetylsalicylic acid in primary prevention of atherosclerotic cardiovascular disease; (2) dual APT (DAPT) duration after percutaneous coronary intervention (PCI) in patients at high bleeding risk; (3) potent DAPT (P2Y inhibitor) choice in patients who present with an acute coronary syndrome (ACS) and possible DAPT de-escalation strategies after PCI; (4) choice and duration of DAPT in ACS patients who are medically treated without revascularization; (5) pretreatment with DAPT (P2Y inhibitor) before elective or nonelective coronary angiography; (6) perioperative and longer-term APT management in patients who require coronary artery bypass grafting surgery; and (7) use of APT in patients with atrial fibrillation who require oral anticoagulation after PCI or medically managed ACS. These recommendations are all on the basis of systematic reviews and meta-analyses conducted as part of the development of these guidelines, provided in the Supplementary Material. Antiplatelet therapy (APT) is the foundation of treatment and prevention of atherothrombotic events in patients with atherosclerotic cardiovascular disease. Selecting the optimal APT strategies to reduce major adverse cardiovascular events, while balancing bleeding risk, requires ongoing review of clinical trials. Appended, the focused update of the Canadian Cardiovascular Society/Canadian Association of Interventional Cardiology guidelines for the use of APT provides recommendations on the following topics: (1) use of acetylsalicylic acid in primary prevention of atherosclerotic cardiovascular disease; (2) dual APT (DAPT) duration after percutaneous coronary intervention (PCI) in patients at high bleeding risk; (3) potent DAPT (P2Y12 inhibitor) choice in patients who present with an acute coronary syndrome (ACS) and possible DAPT de-escalation strategies after PCI; (4) choice and duration of DAPT in ACS patients who are medically treated without revascularization; (5) pretreatment with DAPT (P2Y12 inhibitor) before elective or nonelective coronary angiography; (6) perioperative and longer-term APT management in patients who require coronary artery bypass grafting surgery; and (7) use of APT in patients with atrial fibrillation who require oral anticoagulation after PCI or medically managed ACS. These recommendations are all on the basis of systematic reviews and meta-analyses conducted as part of the development of these guidelines, provided in the Supplementary Material.Antiplatelet therapy (APT) is the foundation of treatment and prevention of atherothrombotic events in patients with atherosclerotic cardiovascular disease. Selecting the optimal APT strategies to reduce major adverse cardiovascular events, while balancing bleeding risk, requires ongoing review of clinical trials. Appended, the focused update of the Canadian Cardiovascular Society/Canadian Association of Interventional Cardiology guidelines for the use of APT provides recommendations on the following topics: (1) use of acetylsalicylic acid in primary prevention of atherosclerotic cardiovascular disease; (2) dual APT (DAPT) duration after percutaneous coronary intervention (PCI) in patients at high bleeding risk; (3) potent DAPT (P2Y12 inhibitor) choice in patients who present with an acute coronary syndrome (ACS) and possible DAPT de-escalation strategies after PCI; (4) choice and duration of DAPT in ACS patients who are medically treated without revascularization; (5) pretreatment with DAPT (P2Y12 inhibitor) before elective or nonelective coronary angiography; (6) perioperative and longer-term APT management in patients who require coronary artery bypass grafting surgery; and (7) use of APT in patients with atrial fibrillation who require oral anticoagulation after PCI or medically managed ACS. These recommendations are all on the basis of systematic reviews and meta-analyses conducted as part of the development of these guidelines, provided in the Supplementary Material. |
| Author | Fremes, Stephen E. Liu, Shuangbo Lordkipanidzé, Marie Turgeon, Ricky D. Graham, Michelle M. Madan, Mina Mansour, Samer Bewick, David Mehta, Shamir R. Lawler, Patrick Mancini, John Cantor, Warren J. Bagai, Akshay So, Derek F. Welsh, Robert C. Lavoie, Andrea Ackman, Margaret L. Boivin-Proulx, Laurie-Anne Potter, Brian J. Yan, Andrew T. Bagur, Rodrigo Bucci, Claudia Bainey, Kevin R. Geller, Carol Marquis-Gravel, Guillaume Babadagli, Hazal E. Shavadia, Jay Wong, Graham C. Tanguay, Jean-François Belley-Côté, Emilie Elbarouni, Basem |
| Author_xml | – sequence: 1 givenname: Kevin R. orcidid: 0000-0002-5458-4617 surname: Bainey fullname: Bainey, Kevin R. email: kevin.bainey@albertahealthservices.ca organization: Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta, Canada – sequence: 2 givenname: Guillaume surname: Marquis-Gravel fullname: Marquis-Gravel, Guillaume organization: Institut de Cardiologie de Montréal, Université de Montréal, Montréal, Québec, Canada – sequence: 3 givenname: Emilie surname: Belley-Côté fullname: Belley-Côté, Emilie organization: Population Health Research Institute, McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada – sequence: 4 givenname: Ricky D. surname: Turgeon fullname: Turgeon, Ricky D. organization: University of British Columbia, St Paul’s Hospital PHARM-HF Clinic, Vancouver, British Columbia, Canada – sequence: 5 givenname: Margaret L. surname: Ackman fullname: Ackman, Margaret L. organization: Alberta Health Services, Edmonton, Alberta, Canada – sequence: 6 givenname: Hazal E. surname: Babadagli fullname: Babadagli, Hazal E. organization: Pharmacy Services, Alberta Health Services, Mazankowski Alberta Heart Institute, Edmonton, Alberta, Canada – sequence: 7 givenname: David surname: Bewick fullname: Bewick, David organization: Division of Cardiology, Department of Medicine, Dalhousie University, Saint John Regional Hospital, Saint John, New Brunswick, Canada – sequence: 8 givenname: Laurie-Anne surname: Boivin-Proulx fullname: Boivin-Proulx, Laurie-Anne organization: Institut de Cardiologie de Montréal, Université de Montréal, Montréal, Québec, Canada – sequence: 9 givenname: Warren J. surname: Cantor fullname: Cantor, Warren J. organization: Southlake Regional Health Centre, University of Toronto, Toronto, Ontario, Canada – sequence: 10 givenname: Stephen E. surname: Fremes fullname: Fremes, Stephen E. organization: University of Toronto, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada – sequence: 11 givenname: Michelle M. surname: Graham fullname: Graham, Michelle M. organization: Division of Cardiology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada – sequence: 12 givenname: Marie surname: Lordkipanidzé fullname: Lordkipanidzé, Marie organization: Faculté de pharmacie, Université de Montréal, Research Center, Montréal Heart Institute, Montréal, Québec, Canada – sequence: 13 givenname: Mina surname: Madan fullname: Madan, Mina organization: Schulich Heart Centre, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada – sequence: 14 givenname: Samer surname: Mansour fullname: Mansour, Samer organization: Centre Hospitalier de l’Université de Montréal, Montréal, Québec, Canada – sequence: 15 givenname: Shamir R. surname: Mehta fullname: Mehta, Shamir R. organization: Population Health Research Institute, McMaster University, Hamilton Health Sciences, Hamilton, Ontario, Canada – sequence: 16 givenname: Brian J. surname: Potter fullname: Potter, Brian J. organization: Centre Hospitalier de l’Université de Montréal, Montréal, Québec, Canada – sequence: 17 givenname: Jay surname: Shavadia fullname: Shavadia, Jay organization: College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada – sequence: 18 givenname: Derek F. surname: So fullname: So, Derek F. organization: University of Ottawa Heart Institute, Ottawa, Ontario, Canada – sequence: 19 givenname: Jean-François surname: Tanguay fullname: Tanguay, Jean-François organization: Institut de Cardiologie de Montréal, Université de Montréal, Montréal, Québec, Canada – sequence: 20 givenname: Robert C. surname: Welsh fullname: Welsh, Robert C. organization: Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta, Canada – sequence: 21 givenname: Andrew T. surname: Yan fullname: Yan, Andrew T. organization: Division of Cardiology, Unity Health Toronto, St Michael’s Hospital, Toronto, Ontario, Canada – sequence: 22 givenname: Akshay surname: Bagai fullname: Bagai, Akshay organization: Terrence Donnelly Heart Centre, St Michael’s Hospital, University of Toronto, Toronto, Ontario, Canada – sequence: 23 givenname: Rodrigo surname: Bagur fullname: Bagur, Rodrigo organization: London Health Sciences Centre, Western University, London, Ontario, Canada – sequence: 24 givenname: Claudia surname: Bucci fullname: Bucci, Claudia organization: Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada – sequence: 25 givenname: Basem surname: Elbarouni fullname: Elbarouni, Basem organization: Department of Medicine, St Boniface Hospital, University of Manitoba, Winnipeg, Manitoba, Canada – sequence: 26 givenname: Carol surname: Geller fullname: Geller, Carol organization: University of Ottawa, Centretown Community Health Centre, Ottawa, Ontario, Canada – sequence: 27 givenname: Andrea surname: Lavoie fullname: Lavoie, Andrea organization: Prairie Vascular Research Inc, Regina, Saskatchewan, Canada – sequence: 28 givenname: Patrick surname: Lawler fullname: Lawler, Patrick organization: Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, Ontario, Canada – sequence: 29 givenname: Shuangbo surname: Liu fullname: Liu, Shuangbo organization: Department of Medicine, St Boniface Hospital, University of Manitoba, Winnipeg, Manitoba, Canada – sequence: 30 givenname: John surname: Mancini fullname: Mancini, John organization: Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada – sequence: 31 givenname: Graham C. surname: Wong fullname: Wong, Graham C. organization: Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38104631$$D View this record in MEDLINE/PubMed |
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| Publisher_xml | – name: Elsevier Inc |
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