Ischaemic cardiac outcomes in patients with atrial fibrillation treated with vitamin K antagonism or factor Xa inhibition: results from the ROCKET AF trial
We investigated the prevalence of prior myocardial infarction (MI) and incidence of ischaemic cardiovascular (CV) events among atrial fibrillation (AF) patients. In ROCKET AF, 14 264 patients with nonvalvular AF were randomized to rivaroxaban or warfarin. The key efficacy outcome for these analyses...
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Veröffentlicht in: | European heart journal 2014-01, Vol.35 (4), p.233-241 |
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creator | Mahaffey, Kenneth W Stevens, Susanna R White, Harvey D Nessel, Christopher C Goodman, Shaun G Piccini, Jonathan P Patel, Manesh R Becker, Richard C Halperin, Jonathan L Hacke, Werner Singer, Daniel E Hankey, Graeme J Califf, Robert M Fox, Keith A A Breithardt, Günter |
description | We investigated the prevalence of prior myocardial infarction (MI) and incidence of ischaemic cardiovascular (CV) events among atrial fibrillation (AF) patients.
In ROCKET AF, 14 264 patients with nonvalvular AF were randomized to rivaroxaban or warfarin. The key efficacy outcome for these analyses was CV death, MI, and unstable angina (UA). This pre-specified analysis was performed on patients while on treatment. Rates are per 100 patient-years. Overall, 2468 (17%) patients had prior MI at enrollment. Compared with patients without prior MI, these patients were more likely to be male (75 vs. 57%), on aspirin at baseline (47 vs. 34%), have prior congestive heart failure (78 vs. 59%), diabetes (47 vs. 39%), hypertension (94 vs. 90%), higher mean CHADS2 score (3.64 vs. 3.43), and fewer prior strokes or transient ischaemic attacks (46 vs. 54%). CV death, MI, or UA rates tended to be lower in patients assigned rivaroxaban compared with warfarin [2.70 vs. 3.15; hazard ratio (HR) 0.86, 95% confidence interval (CI) 0.73-1.00; P = 0.0509]. CV death, MI, or UA rates were higher in those with prior MI compared with no prior MI (6.68 vs. 2.19; HR 3.04, 95% CI 2.59-3.56) with consistent results for CV death, MI, or UA for rivaroxaban compared with warfarin in prior MI compared with no prior MI (P interaction = 0.10).
Prior MI was common and associated with substantial risk for subsequent cardiac events. Patients with prior MI assigned rivaroxaban compared with warfarin had a non-significant 14% reduction of ischaemic cardiac events. |
doi_str_mv | 10.1093/eurheartj/eht428 |
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In ROCKET AF, 14 264 patients with nonvalvular AF were randomized to rivaroxaban or warfarin. The key efficacy outcome for these analyses was CV death, MI, and unstable angina (UA). This pre-specified analysis was performed on patients while on treatment. Rates are per 100 patient-years. Overall, 2468 (17%) patients had prior MI at enrollment. Compared with patients without prior MI, these patients were more likely to be male (75 vs. 57%), on aspirin at baseline (47 vs. 34%), have prior congestive heart failure (78 vs. 59%), diabetes (47 vs. 39%), hypertension (94 vs. 90%), higher mean CHADS2 score (3.64 vs. 3.43), and fewer prior strokes or transient ischaemic attacks (46 vs. 54%). CV death, MI, or UA rates tended to be lower in patients assigned rivaroxaban compared with warfarin [2.70 vs. 3.15; hazard ratio (HR) 0.86, 95% confidence interval (CI) 0.73-1.00; P = 0.0509]. CV death, MI, or UA rates were higher in those with prior MI compared with no prior MI (6.68 vs. 2.19; HR 3.04, 95% CI 2.59-3.56) with consistent results for CV death, MI, or UA for rivaroxaban compared with warfarin in prior MI compared with no prior MI (P interaction = 0.10).
Prior MI was common and associated with substantial risk for subsequent cardiac events. Patients with prior MI assigned rivaroxaban compared with warfarin had a non-significant 14% reduction of ischaemic cardiac events.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/eurheartj/eht428</identifier><identifier>PMID: 24132190</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject><![CDATA[Aged ; Anticoagulants - administration & dosage ; Aspirin - therapeutic use ; Atrial Fibrillation - complications ; Atrial Fibrillation - drug therapy ; Clinical Research ; Double-Blind Method ; Embolism - prevention & control ; Female ; Humans ; Kaplan-Meier Estimate ; Male ; Morpholines - administration & dosage ; Myocardial Infarction - complications ; Myocardial Infarction - drug therapy ; Platelet Aggregation Inhibitors - therapeutic use ; Pyridines - therapeutic use ; Rivaroxaban ; Stroke - prevention & control ; Thiophenes - administration & dosage ; Ticlopidine - analogs & derivatives ; Ticlopidine - therapeutic use ; Treatment Outcome ; Warfarin - administration & dosage]]></subject><ispartof>European heart journal, 2014-01, Vol.35 (4), p.233-241</ispartof><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2013. For permissions please email: journals.permissions@oup.com 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-c86ef183d0bd2e83b0667f4d0c1de3fc03b4c1a049c638ac3032a05ca21a2e733</citedby><cites>FETCH-LOGICAL-c396t-c86ef183d0bd2e83b0667f4d0c1de3fc03b4c1a049c638ac3032a05ca21a2e733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24132190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mahaffey, Kenneth W</creatorcontrib><creatorcontrib>Stevens, Susanna R</creatorcontrib><creatorcontrib>White, Harvey D</creatorcontrib><creatorcontrib>Nessel, Christopher C</creatorcontrib><creatorcontrib>Goodman, Shaun G</creatorcontrib><creatorcontrib>Piccini, Jonathan P</creatorcontrib><creatorcontrib>Patel, Manesh R</creatorcontrib><creatorcontrib>Becker, Richard C</creatorcontrib><creatorcontrib>Halperin, Jonathan L</creatorcontrib><creatorcontrib>Hacke, Werner</creatorcontrib><creatorcontrib>Singer, Daniel E</creatorcontrib><creatorcontrib>Hankey, Graeme J</creatorcontrib><creatorcontrib>Califf, Robert M</creatorcontrib><creatorcontrib>Fox, Keith A A</creatorcontrib><creatorcontrib>Breithardt, Günter</creatorcontrib><creatorcontrib>ROCKET AF Investigators</creatorcontrib><creatorcontrib>for the ROCKET AF Investigators</creatorcontrib><title>Ischaemic cardiac outcomes in patients with atrial fibrillation treated with vitamin K antagonism or factor Xa inhibition: results from the ROCKET AF trial</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>We investigated the prevalence of prior myocardial infarction (MI) and incidence of ischaemic cardiovascular (CV) events among atrial fibrillation (AF) patients.
In ROCKET AF, 14 264 patients with nonvalvular AF were randomized to rivaroxaban or warfarin. The key efficacy outcome for these analyses was CV death, MI, and unstable angina (UA). This pre-specified analysis was performed on patients while on treatment. Rates are per 100 patient-years. Overall, 2468 (17%) patients had prior MI at enrollment. Compared with patients without prior MI, these patients were more likely to be male (75 vs. 57%), on aspirin at baseline (47 vs. 34%), have prior congestive heart failure (78 vs. 59%), diabetes (47 vs. 39%), hypertension (94 vs. 90%), higher mean CHADS2 score (3.64 vs. 3.43), and fewer prior strokes or transient ischaemic attacks (46 vs. 54%). CV death, MI, or UA rates tended to be lower in patients assigned rivaroxaban compared with warfarin [2.70 vs. 3.15; hazard ratio (HR) 0.86, 95% confidence interval (CI) 0.73-1.00; P = 0.0509]. CV death, MI, or UA rates were higher in those with prior MI compared with no prior MI (6.68 vs. 2.19; HR 3.04, 95% CI 2.59-3.56) with consistent results for CV death, MI, or UA for rivaroxaban compared with warfarin in prior MI compared with no prior MI (P interaction = 0.10).
Prior MI was common and associated with substantial risk for subsequent cardiac events. Patients with prior MI assigned rivaroxaban compared with warfarin had a non-significant 14% reduction of ischaemic cardiac events.</description><subject>Aged</subject><subject>Anticoagulants - administration & dosage</subject><subject>Aspirin - therapeutic use</subject><subject>Atrial Fibrillation - complications</subject><subject>Atrial Fibrillation - drug therapy</subject><subject>Clinical Research</subject><subject>Double-Blind Method</subject><subject>Embolism - prevention & control</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Morpholines - administration & dosage</subject><subject>Myocardial Infarction - complications</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Pyridines - therapeutic use</subject><subject>Rivaroxaban</subject><subject>Stroke - prevention & control</subject><subject>Thiophenes - administration & dosage</subject><subject>Ticlopidine - analogs & derivatives</subject><subject>Ticlopidine - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Warfarin - administration & dosage</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1v1DAQhi0Eokvhzgn5yCXUH1mvwwGpWrVQtVIlVKTerMlk0rhK4sV2ivgt_FlctqzgNId532c-XsbeSvFBikaf0BIHgpjvT2jItbLP2EqulaoaU6-fs5WQzboyxt4esVcp3QshrJHmJTtStdRKNmLFfl0kHIAmjxwhdh6QhyVjmChxP_MdZE9zTvyHzwOHHD2MvPdt9ONYWmHmORJk6vaCB59hKrZLDnOGuzD7NPEQeQ-YS7mFwhx86x-dH3mktIyF3ccw8TwQ_3q9vTy74afn_M-g1-xFD2OiN0_1mH07P7vZfqmurj9fbE-vKtSNyRVaQ720uhNtp8jqVhiz6etOoOxI9yh0W6MEUTdotAXUQisQawQlQdFG62P2ac_dLe1EHZaDI4xuF_0E8acL4N3_ndkP7i48OG0bY40qgPdPgBi-L5Sym3xCKi-aKSzJybpRZiOtqItU7KUYQ0qR-sMYKdxjpu6QqdtnWizv_l3vYPgbov4NqXWlVQ</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Mahaffey, Kenneth W</creator><creator>Stevens, Susanna R</creator><creator>White, Harvey D</creator><creator>Nessel, Christopher C</creator><creator>Goodman, Shaun G</creator><creator>Piccini, Jonathan P</creator><creator>Patel, Manesh R</creator><creator>Becker, Richard C</creator><creator>Halperin, Jonathan L</creator><creator>Hacke, Werner</creator><creator>Singer, Daniel E</creator><creator>Hankey, Graeme J</creator><creator>Califf, Robert M</creator><creator>Fox, Keith A A</creator><creator>Breithardt, Günter</creator><general>Oxford University Press</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Ischaemic cardiac outcomes in patients with atrial fibrillation treated with vitamin K antagonism or factor Xa inhibition: results from the ROCKET AF trial</title><author>Mahaffey, Kenneth W ; Stevens, Susanna R ; White, Harvey D ; Nessel, Christopher C ; Goodman, Shaun G ; Piccini, Jonathan P ; Patel, Manesh R ; Becker, Richard C ; Halperin, Jonathan L ; Hacke, Werner ; Singer, Daniel E ; Hankey, Graeme J ; Califf, Robert M ; Fox, Keith A A ; Breithardt, Günter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-c86ef183d0bd2e83b0667f4d0c1de3fc03b4c1a049c638ac3032a05ca21a2e733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Anticoagulants - administration & dosage</topic><topic>Aspirin - therapeutic use</topic><topic>Atrial Fibrillation - complications</topic><topic>Atrial Fibrillation - drug therapy</topic><topic>Clinical Research</topic><topic>Double-Blind Method</topic><topic>Embolism - prevention & control</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Morpholines - administration & dosage</topic><topic>Myocardial Infarction - complications</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Platelet Aggregation Inhibitors - therapeutic use</topic><topic>Pyridines - therapeutic use</topic><topic>Rivaroxaban</topic><topic>Stroke - prevention & control</topic><topic>Thiophenes - administration & dosage</topic><topic>Ticlopidine - analogs & derivatives</topic><topic>Ticlopidine - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Warfarin - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahaffey, Kenneth W</creatorcontrib><creatorcontrib>Stevens, Susanna R</creatorcontrib><creatorcontrib>White, Harvey D</creatorcontrib><creatorcontrib>Nessel, Christopher C</creatorcontrib><creatorcontrib>Goodman, Shaun G</creatorcontrib><creatorcontrib>Piccini, Jonathan P</creatorcontrib><creatorcontrib>Patel, Manesh R</creatorcontrib><creatorcontrib>Becker, Richard C</creatorcontrib><creatorcontrib>Halperin, Jonathan L</creatorcontrib><creatorcontrib>Hacke, Werner</creatorcontrib><creatorcontrib>Singer, Daniel E</creatorcontrib><creatorcontrib>Hankey, Graeme J</creatorcontrib><creatorcontrib>Califf, Robert M</creatorcontrib><creatorcontrib>Fox, Keith A A</creatorcontrib><creatorcontrib>Breithardt, Günter</creatorcontrib><creatorcontrib>ROCKET AF Investigators</creatorcontrib><creatorcontrib>for the ROCKET AF Investigators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahaffey, Kenneth W</au><au>Stevens, Susanna R</au><au>White, Harvey D</au><au>Nessel, Christopher C</au><au>Goodman, Shaun G</au><au>Piccini, Jonathan P</au><au>Patel, Manesh R</au><au>Becker, Richard C</au><au>Halperin, Jonathan L</au><au>Hacke, Werner</au><au>Singer, Daniel E</au><au>Hankey, Graeme J</au><au>Califf, Robert M</au><au>Fox, Keith A A</au><au>Breithardt, Günter</au><aucorp>ROCKET AF Investigators</aucorp><aucorp>for the ROCKET AF Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ischaemic cardiac outcomes in patients with atrial fibrillation treated with vitamin K antagonism or factor Xa inhibition: results from the ROCKET AF trial</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>35</volume><issue>4</issue><spage>233</spage><epage>241</epage><pages>233-241</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>We investigated the prevalence of prior myocardial infarction (MI) and incidence of ischaemic cardiovascular (CV) events among atrial fibrillation (AF) patients.
In ROCKET AF, 14 264 patients with nonvalvular AF were randomized to rivaroxaban or warfarin. The key efficacy outcome for these analyses was CV death, MI, and unstable angina (UA). This pre-specified analysis was performed on patients while on treatment. Rates are per 100 patient-years. Overall, 2468 (17%) patients had prior MI at enrollment. Compared with patients without prior MI, these patients were more likely to be male (75 vs. 57%), on aspirin at baseline (47 vs. 34%), have prior congestive heart failure (78 vs. 59%), diabetes (47 vs. 39%), hypertension (94 vs. 90%), higher mean CHADS2 score (3.64 vs. 3.43), and fewer prior strokes or transient ischaemic attacks (46 vs. 54%). CV death, MI, or UA rates tended to be lower in patients assigned rivaroxaban compared with warfarin [2.70 vs. 3.15; hazard ratio (HR) 0.86, 95% confidence interval (CI) 0.73-1.00; P = 0.0509]. CV death, MI, or UA rates were higher in those with prior MI compared with no prior MI (6.68 vs. 2.19; HR 3.04, 95% CI 2.59-3.56) with consistent results for CV death, MI, or UA for rivaroxaban compared with warfarin in prior MI compared with no prior MI (P interaction = 0.10).
Prior MI was common and associated with substantial risk for subsequent cardiac events. Patients with prior MI assigned rivaroxaban compared with warfarin had a non-significant 14% reduction of ischaemic cardiac events.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>24132190</pmid><doi>10.1093/eurheartj/eht428</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Aged Anticoagulants - administration & dosage Aspirin - therapeutic use Atrial Fibrillation - complications Atrial Fibrillation - drug therapy Clinical Research Double-Blind Method Embolism - prevention & control Female Humans Kaplan-Meier Estimate Male Morpholines - administration & dosage Myocardial Infarction - complications Myocardial Infarction - drug therapy Platelet Aggregation Inhibitors - therapeutic use Pyridines - therapeutic use Rivaroxaban Stroke - prevention & control Thiophenes - administration & dosage Ticlopidine - analogs & derivatives Ticlopidine - therapeutic use Treatment Outcome Warfarin - administration & dosage |
title | Ischaemic cardiac outcomes in patients with atrial fibrillation treated with vitamin K antagonism or factor Xa inhibition: results from the ROCKET AF trial |
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