Efficacy and Safety of Clopidogrel, Prasugrel and Ticagrelor in ACS Patients Treated with PCI: A Propensity Score Analysis of the RENAMI and BleeMACS Registries
Introduction Real-life data comparing clopidogrel, prasugrel, and ticagrelor for unselected patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS) are lacking, as are data for the temporal distribution of ischemic and bleeding risks. Methods A total of 19,825...
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creator | Peyracchia, Mattia Saglietto, Andrea Biolè, Carloalberto Raposeiras-Roubin, Sergio Abu-Assi, Emad Kinnaird, Tim Ariza-Solé, Albert Liebetrau, Christoph Manzano-Fernández, Sergio Boccuzzi, Giacomo Henriques, Jose Paulo Simao Wilton, Stephen B. Velicki, Lazar Xanthopoulou, Ioanna Correia, Luis Rognoni, Andrea Fabrizio, Ugo Nuñez-Gil, Iván Montabone, Andrea Taha, Salma Fujii, Toshiharu Durante, Alessandro Gili, Sebastiano Magnani, Giulia Autelli, Michele Grosso, Alberto Kawaji, Tetsuma Blanco, Pedro Flores Garay, Alberto Quadri, Giorgio Queija, Berenice Caneiro Huczek, Zenon Paz, Rafael Cobas González-Juanatey, José Ramón Fernández, María Cespón Nie, Shao-Ping D’Amico, Maurizio Pousa, Isabel Muñoz Kawashiri, Masa-aki Gallo, Diego Morbiducci, Umberto Dominguez-Rodriguez, Alberto Lopez-Cuenca, Angel Cequier, Angel Alexopoulos, Dimitrios Iñiguez-Romo, Andrés Grossomarra, Walter Usmiani, Tullio Rinaldi, Mauro D’Ascenzo, Fabrizio |
description | Introduction
Real-life data comparing clopidogrel, prasugrel, and ticagrelor for unselected patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS) are lacking, as are data for the temporal distribution of ischemic and bleeding risks.
Methods
A total of 19,825 patients were enrolled from the RENAMI and BleeMACS registries. Both were multicenter, retrospective, observational registries including the data and outcomes of consecutive patients with ACS who underwent primary PCI and were discharged with dual antiplatelet therapy (DAPT). We evaluated the long-term outcome stratified by the different antiplatelet agents.
Results
A total of 14,105 patients (71.2%) were treated with clopidogrel, 2364 patients (11.9%) with prasugrel and 3356 patients (16.9%) with ticagrelor. After propensity score matching, at 1 year, prasugrel reduced the incidence of net adverse clinical events (NACE; a composite endpoint of all-cause death, myocardial infarction [MI] and Bleeding Academic Research Consortium [BARC] 3–5 bleeding) (4.2% vs.7.6%,
p
= 0.002) and of major adverse cardiovascular events (MACE; a composite endpoint of death and MI) compared with clopidogrel (2.6% vs. 5.2%,
p
= 0.007). Ticagrelor decreased rates of MACE compared with clopidogrel (2.7% vs. 6.2%,
p |
doi_str_mv | 10.1007/s40256-019-00373-1 |
format | Article |
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Real-life data comparing clopidogrel, prasugrel, and ticagrelor for unselected patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS) are lacking, as are data for the temporal distribution of ischemic and bleeding risks.
Methods
A total of 19,825 patients were enrolled from the RENAMI and BleeMACS registries. Both were multicenter, retrospective, observational registries including the data and outcomes of consecutive patients with ACS who underwent primary PCI and were discharged with dual antiplatelet therapy (DAPT). We evaluated the long-term outcome stratified by the different antiplatelet agents.
Results
A total of 14,105 patients (71.2%) were treated with clopidogrel, 2364 patients (11.9%) with prasugrel and 3356 patients (16.9%) with ticagrelor. After propensity score matching, at 1 year, prasugrel reduced the incidence of net adverse clinical events (NACE; a composite endpoint of all-cause death, myocardial infarction [MI] and Bleeding Academic Research Consortium [BARC] 3–5 bleeding) (4.2% vs.7.6%,
p
= 0.002) and of major adverse cardiovascular events (MACE; a composite endpoint of death and MI) compared with clopidogrel (2.6% vs. 5.2%,
p
= 0.007). Ticagrelor decreased rates of MACE compared with clopidogrel (2.7% vs. 6.2%,
p
< 0.001), but not of NACE (6.6% vs. 8.7%,
p
= 0.07). Ticagrelor presented similar performance in terms of MACE compared with prasugrel (2.8% vs. 2.4%,
p
= 0.56), with a trend towards a reduction in MI (0.2% vs. 0.4%,
p
= 0.56), but with higher risk of BARC 3–5 bleedings (3.8% vs. 1.7%,
p
= 0.04). In the daily risk analysis, clopidogrel presented a binomial distribution with a peak of ischemic risk at 3 months, which decreased towards bleedings; prasugrel had a constant equivalence between opposite risks; and ticagrelor constantly reduced recurrent MIs despite higher risk of BARC 3–5 events.
Conclusion
In real life, ticagrelor is more effective in reducing ischemic events during the first year after ACS, despite an increased risk of major bleedings, while prasugrel assures a better balance between ischemic and bleeding recurrent events.</description><identifier>ISSN: 1175-3277</identifier><identifier>EISSN: 1179-187X</identifier><identifier>DOI: 10.1007/s40256-019-00373-1</identifier><identifier>PMID: 31586336</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject><![CDATA[Acute Coronary Syndrome - epidemiology ; Acute Coronary Syndrome - surgery ; Acute coronary syndromes ; Angioplasty ; Cardiology ; Clopidogrel - administration & dosage ; Clopidogrel - adverse effects ; Clopidogrel - pharmacokinetics ; Consortia ; Europe - epidemiology ; Female ; Heart attacks ; Hemorrhage - chemically induced ; Hemorrhage - epidemiology ; Humans ; Male ; Medical imaging ; Medication Therapy Management - statistics & numerical data ; Medicine ; Medicine & Public Health ; Middle Aged ; Mortality ; Myocardial Infarction - epidemiology ; Myocardial Infarction - prevention & control ; Original Research Article ; Patients ; Percutaneous Coronary Intervention - adverse effects ; Percutaneous Coronary Intervention - methods ; Pharmacology/Toxicology ; Pharmacotherapy ; Platelet Aggregation Inhibitors - administration & dosage ; Platelet Aggregation Inhibitors - adverse effects ; Platelet Aggregation Inhibitors - pharmacokinetics ; Prasugrel Hydrochloride - administration & dosage ; Prasugrel Hydrochloride - adverse effects ; Prasugrel Hydrochloride - pharmacokinetics ; Registries - statistics & numerical data ; Risk Adjustment - methods ; Statistical analysis ; Studies ; Therapeutic Equivalency ; Ticagrelor - administration & dosage ; Ticagrelor - adverse effects ; Ticagrelor - pharmacokinetics ; Variables ; Variance analysis]]></subject><ispartof>American journal of cardiovascular drugs : drugs, devices, and other interventions, 2020-06, Vol.20 (3), p.259-269</ispartof><rights>Springer Nature Switzerland AG 2019</rights><rights>Copyright Springer Nature B.V. Jun 2020</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-c718e074eef732a7d0ce8594cc81c9ad0f6d9ed159606a17b56a8fdcec2ffe233</citedby><cites>FETCH-LOGICAL-c375t-c718e074eef732a7d0ce8594cc81c9ad0f6d9ed159606a17b56a8fdcec2ffe233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40256-019-00373-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40256-019-00373-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31586336$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peyracchia, Mattia</creatorcontrib><creatorcontrib>Saglietto, Andrea</creatorcontrib><creatorcontrib>Biolè, Carloalberto</creatorcontrib><creatorcontrib>Raposeiras-Roubin, Sergio</creatorcontrib><creatorcontrib>Abu-Assi, Emad</creatorcontrib><creatorcontrib>Kinnaird, Tim</creatorcontrib><creatorcontrib>Ariza-Solé, Albert</creatorcontrib><creatorcontrib>Liebetrau, Christoph</creatorcontrib><creatorcontrib>Manzano-Fernández, Sergio</creatorcontrib><creatorcontrib>Boccuzzi, Giacomo</creatorcontrib><creatorcontrib>Henriques, Jose Paulo Simao</creatorcontrib><creatorcontrib>Wilton, Stephen B.</creatorcontrib><creatorcontrib>Velicki, Lazar</creatorcontrib><creatorcontrib>Xanthopoulou, Ioanna</creatorcontrib><creatorcontrib>Correia, Luis</creatorcontrib><creatorcontrib>Rognoni, Andrea</creatorcontrib><creatorcontrib>Fabrizio, Ugo</creatorcontrib><creatorcontrib>Nuñez-Gil, Iván</creatorcontrib><creatorcontrib>Montabone, Andrea</creatorcontrib><creatorcontrib>Taha, Salma</creatorcontrib><creatorcontrib>Fujii, Toshiharu</creatorcontrib><creatorcontrib>Durante, Alessandro</creatorcontrib><creatorcontrib>Gili, Sebastiano</creatorcontrib><creatorcontrib>Magnani, Giulia</creatorcontrib><creatorcontrib>Autelli, Michele</creatorcontrib><creatorcontrib>Grosso, Alberto</creatorcontrib><creatorcontrib>Kawaji, Tetsuma</creatorcontrib><creatorcontrib>Blanco, Pedro Flores</creatorcontrib><creatorcontrib>Garay, Alberto</creatorcontrib><creatorcontrib>Quadri, Giorgio</creatorcontrib><creatorcontrib>Queija, Berenice Caneiro</creatorcontrib><creatorcontrib>Huczek, Zenon</creatorcontrib><creatorcontrib>Paz, Rafael Cobas</creatorcontrib><creatorcontrib>González-Juanatey, José Ramón</creatorcontrib><creatorcontrib>Fernández, María Cespón</creatorcontrib><creatorcontrib>Nie, Shao-Ping</creatorcontrib><creatorcontrib>D’Amico, Maurizio</creatorcontrib><creatorcontrib>Pousa, Isabel Muñoz</creatorcontrib><creatorcontrib>Kawashiri, Masa-aki</creatorcontrib><creatorcontrib>Gallo, Diego</creatorcontrib><creatorcontrib>Morbiducci, Umberto</creatorcontrib><creatorcontrib>Dominguez-Rodriguez, Alberto</creatorcontrib><creatorcontrib>Lopez-Cuenca, Angel</creatorcontrib><creatorcontrib>Cequier, Angel</creatorcontrib><creatorcontrib>Alexopoulos, Dimitrios</creatorcontrib><creatorcontrib>Iñiguez-Romo, Andrés</creatorcontrib><creatorcontrib>Grossomarra, Walter</creatorcontrib><creatorcontrib>Usmiani, Tullio</creatorcontrib><creatorcontrib>Rinaldi, Mauro</creatorcontrib><creatorcontrib>D’Ascenzo, Fabrizio</creatorcontrib><title>Efficacy and Safety of Clopidogrel, Prasugrel and Ticagrelor in ACS Patients Treated with PCI: A Propensity Score Analysis of the RENAMI and BleeMACS Registries</title><title>American journal of cardiovascular drugs : drugs, devices, and other interventions</title><addtitle>Am J Cardiovasc Drugs</addtitle><addtitle>Am J Cardiovasc Drugs</addtitle><description>Introduction
Real-life data comparing clopidogrel, prasugrel, and ticagrelor for unselected patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS) are lacking, as are data for the temporal distribution of ischemic and bleeding risks.
Methods
A total of 19,825 patients were enrolled from the RENAMI and BleeMACS registries. Both were multicenter, retrospective, observational registries including the data and outcomes of consecutive patients with ACS who underwent primary PCI and were discharged with dual antiplatelet therapy (DAPT). We evaluated the long-term outcome stratified by the different antiplatelet agents.
Results
A total of 14,105 patients (71.2%) were treated with clopidogrel, 2364 patients (11.9%) with prasugrel and 3356 patients (16.9%) with ticagrelor. After propensity score matching, at 1 year, prasugrel reduced the incidence of net adverse clinical events (NACE; a composite endpoint of all-cause death, myocardial infarction [MI] and Bleeding Academic Research Consortium [BARC] 3–5 bleeding) (4.2% vs.7.6%,
p
= 0.002) and of major adverse cardiovascular events (MACE; a composite endpoint of death and MI) compared with clopidogrel (2.6% vs. 5.2%,
p
= 0.007). Ticagrelor decreased rates of MACE compared with clopidogrel (2.7% vs. 6.2%,
p
< 0.001), but not of NACE (6.6% vs. 8.7%,
p
= 0.07). Ticagrelor presented similar performance in terms of MACE compared with prasugrel (2.8% vs. 2.4%,
p
= 0.56), with a trend towards a reduction in MI (0.2% vs. 0.4%,
p
= 0.56), but with higher risk of BARC 3–5 bleedings (3.8% vs. 1.7%,
p
= 0.04). In the daily risk analysis, clopidogrel presented a binomial distribution with a peak of ischemic risk at 3 months, which decreased towards bleedings; prasugrel had a constant equivalence between opposite risks; and ticagrelor constantly reduced recurrent MIs despite higher risk of BARC 3–5 events.
Conclusion
In real life, ticagrelor is more effective in reducing ischemic events during the first year after ACS, despite an increased risk of major bleedings, while prasugrel assures a better balance between ischemic and bleeding recurrent events.</description><subject>Acute Coronary Syndrome - epidemiology</subject><subject>Acute Coronary Syndrome - surgery</subject><subject>Acute coronary syndromes</subject><subject>Angioplasty</subject><subject>Cardiology</subject><subject>Clopidogrel - administration & dosage</subject><subject>Clopidogrel - adverse effects</subject><subject>Clopidogrel - pharmacokinetics</subject><subject>Consortia</subject><subject>Europe - epidemiology</subject><subject>Female</subject><subject>Heart attacks</subject><subject>Hemorrhage - chemically induced</subject><subject>Hemorrhage - epidemiology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medication Therapy Management - statistics & numerical data</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Myocardial Infarction - epidemiology</subject><subject>Myocardial Infarction - prevention & control</subject><subject>Original Research Article</subject><subject>Patients</subject><subject>Percutaneous Coronary Intervention - adverse effects</subject><subject>Percutaneous Coronary Intervention - methods</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacotherapy</subject><subject>Platelet Aggregation Inhibitors - administration & dosage</subject><subject>Platelet Aggregation Inhibitors - adverse effects</subject><subject>Platelet Aggregation Inhibitors - pharmacokinetics</subject><subject>Prasugrel Hydrochloride - administration & dosage</subject><subject>Prasugrel Hydrochloride - adverse effects</subject><subject>Prasugrel Hydrochloride - pharmacokinetics</subject><subject>Registries - statistics & numerical data</subject><subject>Risk Adjustment - methods</subject><subject>Statistical analysis</subject><subject>Studies</subject><subject>Therapeutic Equivalency</subject><subject>Ticagrelor - administration & dosage</subject><subject>Ticagrelor - adverse effects</subject><subject>Ticagrelor - pharmacokinetics</subject><subject>Variables</subject><subject>Variance analysis</subject><issn>1175-3277</issn><issn>1179-187X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kdFu0zAUhi0EYmPwAlwgS9wS8ImTOOEuRAUqbVCtReLO8uzjzlMWF9sV6tvwqDjtgDuufCx__3cs_YS8BPYWGBPvYsXKuikYdAVjXPACHpFzANEV0Irvj49zXfBSiDPyLMY7xkCUontKzjjUbcN5c05-Lax1WukDVZOha2UxHai3dBj9zhm_DTi-oaug4n4ej9Am8_PFB-om2g9rulLJ4ZQi3QRUCQ396dItXQ3L97TPYb_DKbrsXWsfkPaTGg_RxXlNukV6vfjSXy2P6g8j4tVsvMatiyk4jM_JE6vGiC8ezgvy7eNiM3wuLr9-Wg79ZaG5qFOhBbTIRIVoBS-VMExjW3eV1i3oThlmG9OhgbprWKNA3NSNaq3RqEtrseT8grw-eXfB_9hjTPLO70P-apRlBazlLVQiU-WJ0sHHGNDKXXD3KhwkMDmXIk-lyFyKPJYiIYdePaj3N_do_kb-tJABfgJifpq2GP7t_o_2NxXjl_8</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Peyracchia, Mattia</creator><creator>Saglietto, Andrea</creator><creator>Biolè, Carloalberto</creator><creator>Raposeiras-Roubin, Sergio</creator><creator>Abu-Assi, 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B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20200601</creationdate><title>Efficacy and Safety of Clopidogrel, Prasugrel and Ticagrelor in ACS Patients Treated with PCI: A Propensity Score Analysis of the RENAMI and BleeMACS Registries</title><author>Peyracchia, Mattia ; Saglietto, Andrea ; Biolè, Carloalberto ; Raposeiras-Roubin, Sergio ; Abu-Assi, Emad ; Kinnaird, Tim ; Ariza-Solé, Albert ; Liebetrau, Christoph ; Manzano-Fernández, Sergio ; Boccuzzi, Giacomo ; Henriques, Jose Paulo Simao ; Wilton, Stephen B. ; Velicki, Lazar ; Xanthopoulou, Ioanna ; Correia, Luis ; Rognoni, Andrea ; Fabrizio, Ugo ; Nuñez-Gil, Iván ; Montabone, Andrea ; Taha, Salma ; Fujii, Toshiharu ; Durante, Alessandro ; Gili, Sebastiano ; Magnani, Giulia ; Autelli, Michele ; Grosso, Alberto ; Kawaji, Tetsuma ; Blanco, Pedro Flores ; Garay, Alberto ; Quadri, Giorgio ; Queija, Berenice Caneiro ; Huczek, Zenon ; Paz, Rafael Cobas ; González-Juanatey, José Ramón ; Fernández, María Cespón ; Nie, Shao-Ping ; D’Amico, Maurizio ; Pousa, Isabel Muñoz ; Kawashiri, Masa-aki ; Gallo, Diego ; Morbiducci, Umberto ; Dominguez-Rodriguez, Alberto ; Lopez-Cuenca, Angel ; Cequier, Angel ; Alexopoulos, Dimitrios ; Iñiguez-Romo, Andrés ; Grossomarra, Walter ; Usmiani, Tullio ; Rinaldi, Mauro ; D’Ascenzo, Fabrizio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-c718e074eef732a7d0ce8594cc81c9ad0f6d9ed159606a17b56a8fdcec2ffe233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acute Coronary Syndrome - epidemiology</topic><topic>Acute Coronary Syndrome - surgery</topic><topic>Acute coronary syndromes</topic><topic>Angioplasty</topic><topic>Cardiology</topic><topic>Clopidogrel - administration & dosage</topic><topic>Clopidogrel - adverse effects</topic><topic>Clopidogrel - pharmacokinetics</topic><topic>Consortia</topic><topic>Europe - epidemiology</topic><topic>Female</topic><topic>Heart attacks</topic><topic>Hemorrhage - chemically induced</topic><topic>Hemorrhage - epidemiology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Medication Therapy Management - statistics & numerical data</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Myocardial Infarction - epidemiology</topic><topic>Myocardial Infarction - prevention & control</topic><topic>Original Research Article</topic><topic>Patients</topic><topic>Percutaneous Coronary Intervention - adverse effects</topic><topic>Percutaneous Coronary Intervention - methods</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacotherapy</topic><topic>Platelet Aggregation Inhibitors - administration & dosage</topic><topic>Platelet Aggregation Inhibitors - adverse effects</topic><topic>Platelet Aggregation Inhibitors - pharmacokinetics</topic><topic>Prasugrel Hydrochloride - administration & dosage</topic><topic>Prasugrel Hydrochloride - adverse effects</topic><topic>Prasugrel Hydrochloride - pharmacokinetics</topic><topic>Registries - statistics & numerical data</topic><topic>Risk Adjustment - methods</topic><topic>Statistical analysis</topic><topic>Studies</topic><topic>Therapeutic Equivalency</topic><topic>Ticagrelor - administration & dosage</topic><topic>Ticagrelor - adverse effects</topic><topic>Ticagrelor - pharmacokinetics</topic><topic>Variables</topic><topic>Variance analysis</topic><toplevel>online_resources</toplevel><creatorcontrib>Peyracchia, Mattia</creatorcontrib><creatorcontrib>Saglietto, Andrea</creatorcontrib><creatorcontrib>Biolè, Carloalberto</creatorcontrib><creatorcontrib>Raposeiras-Roubin, Sergio</creatorcontrib><creatorcontrib>Abu-Assi, Emad</creatorcontrib><creatorcontrib>Kinnaird, Tim</creatorcontrib><creatorcontrib>Ariza-Solé, Albert</creatorcontrib><creatorcontrib>Liebetrau, Christoph</creatorcontrib><creatorcontrib>Manzano-Fernández, Sergio</creatorcontrib><creatorcontrib>Boccuzzi, Giacomo</creatorcontrib><creatorcontrib>Henriques, Jose Paulo Simao</creatorcontrib><creatorcontrib>Wilton, Stephen B.</creatorcontrib><creatorcontrib>Velicki, Lazar</creatorcontrib><creatorcontrib>Xanthopoulou, Ioanna</creatorcontrib><creatorcontrib>Correia, Luis</creatorcontrib><creatorcontrib>Rognoni, Andrea</creatorcontrib><creatorcontrib>Fabrizio, Ugo</creatorcontrib><creatorcontrib>Nuñez-Gil, Iván</creatorcontrib><creatorcontrib>Montabone, Andrea</creatorcontrib><creatorcontrib>Taha, Salma</creatorcontrib><creatorcontrib>Fujii, Toshiharu</creatorcontrib><creatorcontrib>Durante, Alessandro</creatorcontrib><creatorcontrib>Gili, Sebastiano</creatorcontrib><creatorcontrib>Magnani, Giulia</creatorcontrib><creatorcontrib>Autelli, Michele</creatorcontrib><creatorcontrib>Grosso, Alberto</creatorcontrib><creatorcontrib>Kawaji, Tetsuma</creatorcontrib><creatorcontrib>Blanco, Pedro Flores</creatorcontrib><creatorcontrib>Garay, Alberto</creatorcontrib><creatorcontrib>Quadri, Giorgio</creatorcontrib><creatorcontrib>Queija, Berenice Caneiro</creatorcontrib><creatorcontrib>Huczek, Zenon</creatorcontrib><creatorcontrib>Paz, Rafael Cobas</creatorcontrib><creatorcontrib>González-Juanatey, José Ramón</creatorcontrib><creatorcontrib>Fernández, María Cespón</creatorcontrib><creatorcontrib>Nie, Shao-Ping</creatorcontrib><creatorcontrib>D’Amico, Maurizio</creatorcontrib><creatorcontrib>Pousa, Isabel Muñoz</creatorcontrib><creatorcontrib>Kawashiri, Masa-aki</creatorcontrib><creatorcontrib>Gallo, Diego</creatorcontrib><creatorcontrib>Morbiducci, Umberto</creatorcontrib><creatorcontrib>Dominguez-Rodriguez, Alberto</creatorcontrib><creatorcontrib>Lopez-Cuenca, Angel</creatorcontrib><creatorcontrib>Cequier, Angel</creatorcontrib><creatorcontrib>Alexopoulos, Dimitrios</creatorcontrib><creatorcontrib>Iñiguez-Romo, Andrés</creatorcontrib><creatorcontrib>Grossomarra, Walter</creatorcontrib><creatorcontrib>Usmiani, Tullio</creatorcontrib><creatorcontrib>Rinaldi, Mauro</creatorcontrib><creatorcontrib>D’Ascenzo, Fabrizio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>American journal of cardiovascular drugs : drugs, devices, and other interventions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peyracchia, Mattia</au><au>Saglietto, Andrea</au><au>Biolè, Carloalberto</au><au>Raposeiras-Roubin, Sergio</au><au>Abu-Assi, Emad</au><au>Kinnaird, Tim</au><au>Ariza-Solé, Albert</au><au>Liebetrau, Christoph</au><au>Manzano-Fernández, Sergio</au><au>Boccuzzi, Giacomo</au><au>Henriques, Jose Paulo Simao</au><au>Wilton, Stephen B.</au><au>Velicki, Lazar</au><au>Xanthopoulou, Ioanna</au><au>Correia, Luis</au><au>Rognoni, Andrea</au><au>Fabrizio, Ugo</au><au>Nuñez-Gil, Iván</au><au>Montabone, Andrea</au><au>Taha, Salma</au><au>Fujii, Toshiharu</au><au>Durante, Alessandro</au><au>Gili, Sebastiano</au><au>Magnani, Giulia</au><au>Autelli, Michele</au><au>Grosso, Alberto</au><au>Kawaji, Tetsuma</au><au>Blanco, Pedro Flores</au><au>Garay, Alberto</au><au>Quadri, Giorgio</au><au>Queija, Berenice Caneiro</au><au>Huczek, Zenon</au><au>Paz, Rafael Cobas</au><au>González-Juanatey, José Ramón</au><au>Fernández, María Cespón</au><au>Nie, Shao-Ping</au><au>D’Amico, Maurizio</au><au>Pousa, Isabel Muñoz</au><au>Kawashiri, Masa-aki</au><au>Gallo, Diego</au><au>Morbiducci, Umberto</au><au>Dominguez-Rodriguez, Alberto</au><au>Lopez-Cuenca, Angel</au><au>Cequier, Angel</au><au>Alexopoulos, Dimitrios</au><au>Iñiguez-Romo, Andrés</au><au>Grossomarra, Walter</au><au>Usmiani, Tullio</au><au>Rinaldi, Mauro</au><au>D’Ascenzo, Fabrizio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and Safety of Clopidogrel, Prasugrel and Ticagrelor in ACS Patients Treated with PCI: A Propensity Score Analysis of the RENAMI and BleeMACS Registries</atitle><jtitle>American journal of cardiovascular drugs : drugs, devices, and other interventions</jtitle><stitle>Am J Cardiovasc Drugs</stitle><addtitle>Am J Cardiovasc Drugs</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>20</volume><issue>3</issue><spage>259</spage><epage>269</epage><pages>259-269</pages><issn>1175-3277</issn><eissn>1179-187X</eissn><abstract>Introduction
Real-life data comparing clopidogrel, prasugrel, and ticagrelor for unselected patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS) are lacking, as are data for the temporal distribution of ischemic and bleeding risks.
Methods
A total of 19,825 patients were enrolled from the RENAMI and BleeMACS registries. Both were multicenter, retrospective, observational registries including the data and outcomes of consecutive patients with ACS who underwent primary PCI and were discharged with dual antiplatelet therapy (DAPT). We evaluated the long-term outcome stratified by the different antiplatelet agents.
Results
A total of 14,105 patients (71.2%) were treated with clopidogrel, 2364 patients (11.9%) with prasugrel and 3356 patients (16.9%) with ticagrelor. After propensity score matching, at 1 year, prasugrel reduced the incidence of net adverse clinical events (NACE; a composite endpoint of all-cause death, myocardial infarction [MI] and Bleeding Academic Research Consortium [BARC] 3–5 bleeding) (4.2% vs.7.6%,
p
= 0.002) and of major adverse cardiovascular events (MACE; a composite endpoint of death and MI) compared with clopidogrel (2.6% vs. 5.2%,
p
= 0.007). Ticagrelor decreased rates of MACE compared with clopidogrel (2.7% vs. 6.2%,
p
< 0.001), but not of NACE (6.6% vs. 8.7%,
p
= 0.07). Ticagrelor presented similar performance in terms of MACE compared with prasugrel (2.8% vs. 2.4%,
p
= 0.56), with a trend towards a reduction in MI (0.2% vs. 0.4%,
p
= 0.56), but with higher risk of BARC 3–5 bleedings (3.8% vs. 1.7%,
p
= 0.04). In the daily risk analysis, clopidogrel presented a binomial distribution with a peak of ischemic risk at 3 months, which decreased towards bleedings; prasugrel had a constant equivalence between opposite risks; and ticagrelor constantly reduced recurrent MIs despite higher risk of BARC 3–5 events.
Conclusion
In real life, ticagrelor is more effective in reducing ischemic events during the first year after ACS, despite an increased risk of major bleedings, while prasugrel assures a better balance between ischemic and bleeding recurrent events.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>31586336</pmid><doi>10.1007/s40256-019-00373-1</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1175-3277 |
ispartof | American journal of cardiovascular drugs : drugs, devices, and other interventions, 2020-06, Vol.20 (3), p.259-269 |
issn | 1175-3277 1179-187X |
language | eng |
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source | MEDLINE; SpringerLink Journals |
subjects | Acute Coronary Syndrome - epidemiology Acute Coronary Syndrome - surgery Acute coronary syndromes Angioplasty Cardiology Clopidogrel - administration & dosage Clopidogrel - adverse effects Clopidogrel - pharmacokinetics Consortia Europe - epidemiology Female Heart attacks Hemorrhage - chemically induced Hemorrhage - epidemiology Humans Male Medical imaging Medication Therapy Management - statistics & numerical data Medicine Medicine & Public Health Middle Aged Mortality Myocardial Infarction - epidemiology Myocardial Infarction - prevention & control Original Research Article Patients Percutaneous Coronary Intervention - adverse effects Percutaneous Coronary Intervention - methods Pharmacology/Toxicology Pharmacotherapy Platelet Aggregation Inhibitors - administration & dosage Platelet Aggregation Inhibitors - adverse effects Platelet Aggregation Inhibitors - pharmacokinetics Prasugrel Hydrochloride - administration & dosage Prasugrel Hydrochloride - adverse effects Prasugrel Hydrochloride - pharmacokinetics Registries - statistics & numerical data Risk Adjustment - methods Statistical analysis Studies Therapeutic Equivalency Ticagrelor - administration & dosage Ticagrelor - adverse effects Ticagrelor - pharmacokinetics Variables Variance analysis |
title | Efficacy and Safety of Clopidogrel, Prasugrel and Ticagrelor in ACS Patients Treated with PCI: A Propensity Score Analysis of the RENAMI and BleeMACS Registries |
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