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Evaluation of survival and ischaemic and thromboembolic event rates in patients with non-valvar atrial fibrillation in the general population when treated and untreated with warfarin
Objective: To compare survival and adverse outcome of patients with non-valvar atrial fibrillation (NVAF) treated with or without warfarin. Design: Record linkage method to identify patients with a previous hospital diagnosis of atrial fibrillation and to link these patients to international normali...
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Published in: | Heart (British Cardiac Society) 2006-02, Vol.92 (2), p.196-200 |
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description | Objective: To compare survival and adverse outcome of patients with non-valvar atrial fibrillation (NVAF) treated with or without warfarin. Design: Record linkage method to identify patients with a previous hospital diagnosis of atrial fibrillation and to link these patients to international normalised ratio (INR) test results and mortality data. Setting: Cardiff and the Vale of Glamorgan, Wales. Main outcome measures: Mortality, specifically from ischaemic and thromboembolic events. Results: 6108 patients were identified with NVAF, of whom 36.4% received warfarin. Mean survival in the warfarin and non-warfarin groups was 52.0 months and 38.2 months, respectively (p < 0.001), and 14.4 months (p < 0.001) after adjustment for confounding factors. Warfarin treated patients in the upper quartile of INR control had significantly longer survival (57.5 months) than did those in the lowest quartile of control (38.1 months, p < 0.001). The risk of stroke in the warfarin group when treated was lower than that in the non-warfarin group (relative rate (RR) 0.74, p < 0.001). The risk of death from ischaemic stroke was lower in the warfarin group (RR 0.43, p < 0.001). The risk of all ischaemic and embolic events in the warfarin group was lower when they were taking warfarin (RR 0.74, p < 0.001). The risk of bleeding in the warfarin group when treated was greater (RR 1.78, p = 0.001). Conclusions: Patients with NVAF within the recommended target INR range of 2.0–3.0 survive longer and have reduced morbidity. Probably too few people are anticoagulated with warfarin in NVAF. |
doi_str_mv | 10.1136/hrt.2004.058339 |
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Design: Record linkage method to identify patients with a previous hospital diagnosis of atrial fibrillation and to link these patients to international normalised ratio (INR) test results and mortality data. Setting: Cardiff and the Vale of Glamorgan, Wales. Main outcome measures: Mortality, specifically from ischaemic and thromboembolic events. Results: 6108 patients were identified with NVAF, of whom 36.4% received warfarin. Mean survival in the warfarin and non-warfarin groups was 52.0 months and 38.2 months, respectively (p < 0.001), and 14.4 months (p < 0.001) after adjustment for confounding factors. Warfarin treated patients in the upper quartile of INR control had significantly longer survival (57.5 months) than did those in the lowest quartile of control (38.1 months, p < 0.001). The risk of stroke in the warfarin group when treated was lower than that in the non-warfarin group (relative rate (RR) 0.74, p < 0.001). The risk of death from ischaemic stroke was lower in the warfarin group (RR 0.43, p < 0.001). The risk of all ischaemic and embolic events in the warfarin group was lower when they were taking warfarin (RR 0.74, p < 0.001). The risk of bleeding in the warfarin group when treated was greater (RR 1.78, p = 0.001). Conclusions: Patients with NVAF within the recommended target INR range of 2.0–3.0 survive longer and have reduced morbidity. Probably too few people are anticoagulated with warfarin in NVAF.]]></description><identifier>ISSN: 1355-6037</identifier><identifier>EISSN: 1468-201X</identifier><identifier>DOI: 10.1136/hrt.2004.058339</identifier><identifier>PMID: 15883133</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Cardiovascular Society</publisher><subject>10th revision ; Aged ; Aged, 80 and over ; Anticoagulants - therapeutic use ; anticoagulation ; atrial fibrillation ; Atrial Fibrillation - drug therapy ; Atrial Fibrillation - mortality ; Biological and medical sciences ; Blood and lymphatic vessels ; Brain Ischemia - mortality ; Brain Ischemia - prevention & control ; Cardiac dysrhythmias ; Cardiology. Vascular system ; Cardiovascular Medicine ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Epidemiology ; Female ; Health risk assessment ; Heart ; Heart attacks ; Hospitals ; Humans ; ICD-10 ; INR ; International classification of diseases ; international normalised ratio ; International Normalized Ratio ; Male ; Medical sciences ; Morbidity ; Mortality ; non-valvar atrial fibrillation ; NVAF ; Population ; Reading ; relative rate ; Stroke ; Survival Analysis ; Thromboembolism ; Thromboembolism - mortality ; Thromboembolism - prevention & control ; warfarin ; Warfarin - therapeutic use</subject><ispartof>Heart (British Cardiac Society), 2006-02, Vol.92 (2), p.196-200</ispartof><rights>Copyright 2006 by Heart</rights><rights>2006 INIST-CNRS</rights><rights>Copyright: 2006 Copyright 2006 by Heart</rights><rights>Copyright © 2006 BMJ Publishing Group and British Cardiovascular Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b522t-976a9ab542d41bc718ed2ed89dc2b2c2fa8feaeacb9a632a06b72043fb59b0e63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1860757/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1860757/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17434349$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15883133$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Currie, C J</creatorcontrib><creatorcontrib>Jones, M</creatorcontrib><creatorcontrib>Goodfellow, J</creatorcontrib><creatorcontrib>McEwan, P</creatorcontrib><creatorcontrib>Morgan, C L</creatorcontrib><creatorcontrib>Emmas, C</creatorcontrib><creatorcontrib>Peters, J R</creatorcontrib><title>Evaluation of survival and ischaemic and thromboembolic event rates in patients with non-valvar atrial fibrillation in the general population when treated and untreated with warfarin</title><title>Heart (British Cardiac Society)</title><addtitle>Heart</addtitle><description><![CDATA[Objective: To compare survival and adverse outcome of patients with non-valvar atrial fibrillation (NVAF) treated with or without warfarin. Design: Record linkage method to identify patients with a previous hospital diagnosis of atrial fibrillation and to link these patients to international normalised ratio (INR) test results and mortality data. Setting: Cardiff and the Vale of Glamorgan, Wales. Main outcome measures: Mortality, specifically from ischaemic and thromboembolic events. Results: 6108 patients were identified with NVAF, of whom 36.4% received warfarin. Mean survival in the warfarin and non-warfarin groups was 52.0 months and 38.2 months, respectively (p < 0.001), and 14.4 months (p < 0.001) after adjustment for confounding factors. Warfarin treated patients in the upper quartile of INR control had significantly longer survival (57.5 months) than did those in the lowest quartile of control (38.1 months, p < 0.001). The risk of stroke in the warfarin group when treated was lower than that in the non-warfarin group (relative rate (RR) 0.74, p < 0.001). The risk of death from ischaemic stroke was lower in the warfarin group (RR 0.43, p < 0.001). The risk of all ischaemic and embolic events in the warfarin group was lower when they were taking warfarin (RR 0.74, p < 0.001). The risk of bleeding in the warfarin group when treated was greater (RR 1.78, p = 0.001). Conclusions: Patients with NVAF within the recommended target INR range of 2.0–3.0 survive longer and have reduced morbidity. Probably too few people are anticoagulated with warfarin in NVAF.]]></description><subject>10th revision</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anticoagulants - therapeutic use</subject><subject>anticoagulation</subject><subject>atrial fibrillation</subject><subject>Atrial Fibrillation - drug therapy</subject><subject>Atrial Fibrillation - mortality</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Brain Ischemia - mortality</subject><subject>Brain Ischemia - prevention & control</subject><subject>Cardiac dysrhythmias</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular Medicine</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Heart</subject><subject>Heart attacks</subject><subject>Hospitals</subject><subject>Humans</subject><subject>ICD-10</subject><subject>INR</subject><subject>International classification of diseases</subject><subject>international normalised ratio</subject><subject>International Normalized Ratio</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>non-valvar atrial fibrillation</subject><subject>NVAF</subject><subject>Population</subject><subject>Reading</subject><subject>relative rate</subject><subject>Stroke</subject><subject>Survival Analysis</subject><subject>Thromboembolism</subject><subject>Thromboembolism - mortality</subject><subject>Thromboembolism - prevention & control</subject><subject>warfarin</subject><subject>Warfarin - therapeutic use</subject><issn>1355-6037</issn><issn>1468-201X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkl-L1DAUxYso7rr67JsERB-EzuZPm6Qvggy7s8KiCCr7FpI23WZsk9mkndUv5ufzznTcVV-klDb3_HJybzhZ9pzgBSGMn3ZxXFCMiwUuJWPVg-yYFFzmFJOrh_DPyjLnmImj7ElKawxgJfnj7IiUUjLC2HH282yr-0mPLngUWpSmuHVQQdo3yKW603Zw9X41djEMJlh4eyjZrfUjinq0CTmPNmABhYRu3dghH3wOLlsdkR6jA7_Wmej6fj4I-LGz6Np6G0HbhM10UG47C1q0YNvsT53879Xe-FbHVkfnn2aPWt0n--zwPcm-nJ99Xl7klx9X75fvLnNTUjrmleC60qYsaFMQUwsibUNtI6umpobWtNWytdrq2lSaM6oxN4LigrWmrAy2nJ1kb2ffzWQG29QwInSsNtENOv5QQTv1t-Jdp67DVhHJsSgFGLw-GMRwM9k0qgGu1cJNeBumpATmUpRVBeDLf8B1mKKH4RQREnPBJMVAnc5UHUNK0bZ3rRCsdolQkAi1S4SaEwE7Xvw5wT1_iAAArw6ATrXu26h97dI9JwoGz84onzmXRvv9Ttfxm4LmRKk-fF2qq2K1-nQhuDoH_s3Mm2H93y5_ATJP4hw</recordid><startdate>20060201</startdate><enddate>20060201</enddate><creator>Currie, C J</creator><creator>Jones, M</creator><creator>Goodfellow, J</creator><creator>McEwan, P</creator><creator>Morgan, C L</creator><creator>Emmas, C</creator><creator>Peters, J R</creator><general>BMJ Publishing Group Ltd and British Cardiovascular Society</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20060201</creationdate><title>Evaluation of survival and ischaemic and thromboembolic event rates in patients with non-valvar atrial fibrillation in the general population when treated and untreated with warfarin</title><author>Currie, C J ; Jones, M ; Goodfellow, J ; McEwan, P ; Morgan, C L ; Emmas, C ; Peters, J R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b522t-976a9ab542d41bc718ed2ed89dc2b2c2fa8feaeacb9a632a06b72043fb59b0e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>10th revision</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anticoagulants - therapeutic use</topic><topic>anticoagulation</topic><topic>atrial fibrillation</topic><topic>Atrial Fibrillation - drug therapy</topic><topic>Atrial Fibrillation - mortality</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Brain Ischemia - mortality</topic><topic>Brain Ischemia - prevention & control</topic><topic>Cardiac dysrhythmias</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular Medicine</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Health risk assessment</topic><topic>Heart</topic><topic>Heart attacks</topic><topic>Hospitals</topic><topic>Humans</topic><topic>ICD-10</topic><topic>INR</topic><topic>International classification of diseases</topic><topic>international normalised ratio</topic><topic>International Normalized Ratio</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>non-valvar atrial fibrillation</topic><topic>NVAF</topic><topic>Population</topic><topic>Reading</topic><topic>relative rate</topic><topic>Stroke</topic><topic>Survival Analysis</topic><topic>Thromboembolism</topic><topic>Thromboembolism - mortality</topic><topic>Thromboembolism - prevention & control</topic><topic>warfarin</topic><topic>Warfarin - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Currie, C J</creatorcontrib><creatorcontrib>Jones, M</creatorcontrib><creatorcontrib>Goodfellow, J</creatorcontrib><creatorcontrib>McEwan, P</creatorcontrib><creatorcontrib>Morgan, C L</creatorcontrib><creatorcontrib>Emmas, C</creatorcontrib><creatorcontrib>Peters, J R</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science 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><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Heart (British Cardiac Society)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Currie, C J</au><au>Jones, M</au><au>Goodfellow, J</au><au>McEwan, P</au><au>Morgan, C L</au><au>Emmas, C</au><au>Peters, J R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of survival and ischaemic and thromboembolic event rates in patients with non-valvar atrial fibrillation in the general population when treated and untreated with warfarin</atitle><jtitle>Heart (British Cardiac Society)</jtitle><addtitle>Heart</addtitle><date>2006-02-01</date><risdate>2006</risdate><volume>92</volume><issue>2</issue><spage>196</spage><epage>200</epage><pages>196-200</pages><issn>1355-6037</issn><eissn>1468-201X</eissn><abstract><![CDATA[Objective: To compare survival and adverse outcome of patients with non-valvar atrial fibrillation (NVAF) treated with or without warfarin. Design: Record linkage method to identify patients with a previous hospital diagnosis of atrial fibrillation and to link these patients to international normalised ratio (INR) test results and mortality data. Setting: Cardiff and the Vale of Glamorgan, Wales. Main outcome measures: Mortality, specifically from ischaemic and thromboembolic events. Results: 6108 patients were identified with NVAF, of whom 36.4% received warfarin. Mean survival in the warfarin and non-warfarin groups was 52.0 months and 38.2 months, respectively (p < 0.001), and 14.4 months (p < 0.001) after adjustment for confounding factors. Warfarin treated patients in the upper quartile of INR control had significantly longer survival (57.5 months) than did those in the lowest quartile of control (38.1 months, p < 0.001). The risk of stroke in the warfarin group when treated was lower than that in the non-warfarin group (relative rate (RR) 0.74, p < 0.001). The risk of death from ischaemic stroke was lower in the warfarin group (RR 0.43, p < 0.001). The risk of all ischaemic and embolic events in the warfarin group was lower when they were taking warfarin (RR 0.74, p < 0.001). The risk of bleeding in the warfarin group when treated was greater (RR 1.78, p = 0.001). Conclusions: Patients with NVAF within the recommended target INR range of 2.0–3.0 survive longer and have reduced morbidity. Probably too few people are anticoagulated with warfarin in NVAF.]]></abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><pmid>15883133</pmid><doi>10.1136/hrt.2004.058339</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 10th revision Aged Aged, 80 and over Anticoagulants - therapeutic use anticoagulation atrial fibrillation Atrial Fibrillation - drug therapy Atrial Fibrillation - mortality Biological and medical sciences Blood and lymphatic vessels Brain Ischemia - mortality Brain Ischemia - prevention & control Cardiac dysrhythmias Cardiology. Vascular system Cardiovascular Medicine Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Epidemiology Female Health risk assessment Heart Heart attacks Hospitals Humans ICD-10 INR International classification of diseases international normalised ratio International Normalized Ratio Male Medical sciences Morbidity Mortality non-valvar atrial fibrillation NVAF Population Reading relative rate Stroke Survival Analysis Thromboembolism Thromboembolism - mortality Thromboembolism - prevention & control warfarin Warfarin - therapeutic use |
title | Evaluation of survival and ischaemic and thromboembolic event rates in patients with non-valvar atrial fibrillation in the general population when treated and untreated with warfarin |
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