Evaluation of SAMe-TT2R2 risk score for predicting the quality of anticoagulation control in a real-world cohort of patients with non-valvular atrial fibrillation on vitamin-K antagonists
Clinicians need to get better at identifying patients who would have poor quality of anticoagulation control with vitamin-K antagonists (VKAs). We assessed the predictive ability of SAMe-TT2R2 score, recently conceived for the prior purpose, and examined its relationship with major bleeding, thrombo...
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creator | Abumuaileq, Rami Riziq-Yousef Abu-Assi, Emad Raposeiras-Roubin, Sergio López-López, Andrea Redondo-Diéguez, Alfredo Álvarez-Iglesias, Diego Rodríguez-Mañero, Moisés Peña-Gil, Carlos González-Juanatey, Jose Ramón |
description | Clinicians need to get better at identifying patients who would have poor quality of anticoagulation control with vitamin-K antagonists (VKAs). We assessed the predictive ability of SAMe-TT2R2 score, recently conceived for the prior purpose, and examined its relationship with major bleeding, thromboembolic (TE) complications, and death.
Retrospectively, 911 consecutive patients with non-valvular atrial fibrillation (NVAF) started on VKAs within 8 months were studied. The percentage of international normalized ratios in therapeutic range (PINRR) at different levels was used as a metric of anticoagulation quality. We also tested the SAMe-TT2R2 predictability for major bleeding, TE complications, and death throughout 10 ± 3 months. The PINRR decreased from 62% at zero point to 53% at ≥4 points of SAMe-TT2R2. 82.1% of patients who achieved PINRR ≥ 70% had 0 or 1 point of SAMe-TT2R2. SAMe-TT2R2 performed significantly better at PINRR 70% than at 65 and 60% (c-statistic = 0.60 vs. c-statistic = 0.56). The calibration of SAMe-TT2R2 was excellent (Hosmer-Lemeshow test P-values ≥ 0.6). SAMe-TT2R2 showed significant association with the composite outcome of major bleeding, TE complications, and death [n = 98; hazard ratio (HR) = 1.32; 95% confidence interval (CI) 1.08-1.60]; the c-statistic was 0.57 (95% CI: 0.51-0.62) and P = 0.03. As individual outcomes, SAMe-TT2R2 was significantly associated with death (n = 60; HR = 1.3; 95% CI: 1.03-1.69), but not with either major bleeding (n = 30; HR = 1.2; 95% CI: 0.85-1.76) or TE complications (n = 15; HR = 1.01; 95% CI: 0.58-1.77).
Among NVAF patients, SAMe-TT2R2 could represent a useful clinical tool to identify patients who would have poor quality of anticoagulation control with VKAs. SAMe-TT2R2 successfully predicts the composite outcome of major bleeding, TE complications, and death. |
doi_str_mv | 10.1093/europace/euu353 |
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Retrospectively, 911 consecutive patients with non-valvular atrial fibrillation (NVAF) started on VKAs within 8 months were studied. The percentage of international normalized ratios in therapeutic range (PINRR) at different levels was used as a metric of anticoagulation quality. We also tested the SAMe-TT2R2 predictability for major bleeding, TE complications, and death throughout 10 ± 3 months. The PINRR decreased from 62% at zero point to 53% at ≥4 points of SAMe-TT2R2. 82.1% of patients who achieved PINRR ≥ 70% had 0 or 1 point of SAMe-TT2R2. SAMe-TT2R2 performed significantly better at PINRR 70% than at 65 and 60% (c-statistic = 0.60 vs. c-statistic = 0.56). The calibration of SAMe-TT2R2 was excellent (Hosmer-Lemeshow test P-values ≥ 0.6). SAMe-TT2R2 showed significant association with the composite outcome of major bleeding, TE complications, and death [n = 98; hazard ratio (HR) = 1.32; 95% confidence interval (CI) 1.08-1.60]; the c-statistic was 0.57 (95% CI: 0.51-0.62) and P = 0.03. As individual outcomes, SAMe-TT2R2 was significantly associated with death (n = 60; HR = 1.3; 95% CI: 1.03-1.69), but not with either major bleeding (n = 30; HR = 1.2; 95% CI: 0.85-1.76) or TE complications (n = 15; HR = 1.01; 95% CI: 0.58-1.77).
Among NVAF patients, SAMe-TT2R2 could represent a useful clinical tool to identify patients who would have poor quality of anticoagulation control with VKAs. SAMe-TT2R2 successfully predicts the composite outcome of major bleeding, TE complications, and death.</description><identifier>ISSN: 1099-5129</identifier><identifier>EISSN: 1532-2092</identifier><identifier>DOI: 10.1093/europace/euu353</identifier><identifier>PMID: 25662984</identifier><language>eng</language><publisher>England</publisher><subject>Aged ; Aged, 80 and over ; Anticoagulants - adverse effects ; Anticoagulants - therapeutic use ; Atrial Fibrillation - blood ; Atrial Fibrillation - diagnosis ; Atrial Fibrillation - drug therapy ; Atrial Fibrillation - mortality ; Blood Coagulation - drug effects ; Decision Support Techniques ; Drug Monitoring - methods ; Female ; Hemorrhage - chemically induced ; Humans ; International Normalized Ratio ; Male ; Middle Aged ; Patient Selection ; Predictive Value of Tests ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Stroke - blood ; Stroke - diagnosis ; Stroke - mortality ; Stroke - prevention & control ; Thromboembolism - blood ; Thromboembolism - diagnosis ; Thromboembolism - mortality ; Thromboembolism - prevention & control ; Treatment Outcome ; Vitamin K - antagonists & inhibitors</subject><ispartof>Europace (London, England), 2015-05, Vol.17 (5), p.711-717</ispartof><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c297t-48310f9fc9b1275a167157772f098b1de18290c7a3e52f18e5dd44dcebf738823</citedby><cites>FETCH-LOGICAL-c297t-48310f9fc9b1275a167157772f098b1de18290c7a3e52f18e5dd44dcebf738823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25662984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abumuaileq, Rami Riziq-Yousef</creatorcontrib><creatorcontrib>Abu-Assi, Emad</creatorcontrib><creatorcontrib>Raposeiras-Roubin, Sergio</creatorcontrib><creatorcontrib>López-López, Andrea</creatorcontrib><creatorcontrib>Redondo-Diéguez, Alfredo</creatorcontrib><creatorcontrib>Álvarez-Iglesias, Diego</creatorcontrib><creatorcontrib>Rodríguez-Mañero, Moisés</creatorcontrib><creatorcontrib>Peña-Gil, Carlos</creatorcontrib><creatorcontrib>González-Juanatey, Jose Ramón</creatorcontrib><title>Evaluation of SAMe-TT2R2 risk score for predicting the quality of anticoagulation control in a real-world cohort of patients with non-valvular atrial fibrillation on vitamin-K antagonists</title><title>Europace (London, England)</title><addtitle>Europace</addtitle><description>Clinicians need to get better at identifying patients who would have poor quality of anticoagulation control with vitamin-K antagonists (VKAs). We assessed the predictive ability of SAMe-TT2R2 score, recently conceived for the prior purpose, and examined its relationship with major bleeding, thromboembolic (TE) complications, and death.
Retrospectively, 911 consecutive patients with non-valvular atrial fibrillation (NVAF) started on VKAs within 8 months were studied. The percentage of international normalized ratios in therapeutic range (PINRR) at different levels was used as a metric of anticoagulation quality. We also tested the SAMe-TT2R2 predictability for major bleeding, TE complications, and death throughout 10 ± 3 months. The PINRR decreased from 62% at zero point to 53% at ≥4 points of SAMe-TT2R2. 82.1% of patients who achieved PINRR ≥ 70% had 0 or 1 point of SAMe-TT2R2. SAMe-TT2R2 performed significantly better at PINRR 70% than at 65 and 60% (c-statistic = 0.60 vs. c-statistic = 0.56). The calibration of SAMe-TT2R2 was excellent (Hosmer-Lemeshow test P-values ≥ 0.6). SAMe-TT2R2 showed significant association with the composite outcome of major bleeding, TE complications, and death [n = 98; hazard ratio (HR) = 1.32; 95% confidence interval (CI) 1.08-1.60]; the c-statistic was 0.57 (95% CI: 0.51-0.62) and P = 0.03. As individual outcomes, SAMe-TT2R2 was significantly associated with death (n = 60; HR = 1.3; 95% CI: 1.03-1.69), but not with either major bleeding (n = 30; HR = 1.2; 95% CI: 0.85-1.76) or TE complications (n = 15; HR = 1.01; 95% CI: 0.58-1.77).
Among NVAF patients, SAMe-TT2R2 could represent a useful clinical tool to identify patients who would have poor quality of anticoagulation control with VKAs. SAMe-TT2R2 successfully predicts the composite outcome of major bleeding, TE complications, and death.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anticoagulants - adverse effects</subject><subject>Anticoagulants - therapeutic use</subject><subject>Atrial Fibrillation - blood</subject><subject>Atrial Fibrillation - diagnosis</subject><subject>Atrial Fibrillation - drug therapy</subject><subject>Atrial Fibrillation - mortality</subject><subject>Blood Coagulation - drug effects</subject><subject>Decision Support Techniques</subject><subject>Drug Monitoring - methods</subject><subject>Female</subject><subject>Hemorrhage - chemically induced</subject><subject>Humans</subject><subject>International Normalized Ratio</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patient Selection</subject><subject>Predictive Value of Tests</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Stroke - blood</subject><subject>Stroke - diagnosis</subject><subject>Stroke - mortality</subject><subject>Stroke - prevention & control</subject><subject>Thromboembolism - blood</subject><subject>Thromboembolism - diagnosis</subject><subject>Thromboembolism - mortality</subject><subject>Thromboembolism - prevention & control</subject><subject>Treatment Outcome</subject><subject>Vitamin K - antagonists & inhibitors</subject><issn>1099-5129</issn><issn>1532-2092</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kVuLFDEQhRtR3Is--yZ59CW7uXQmyeOyrBdcEXR8btLpykw0k_Qm6Vn2t_nnzDCzQkEVxTlfFZyue0fJFSWaX8OS02wstGHhgr_ozqngDDOi2cs2E62xoEyfdRel_CaESKbF6-6MidWKadWfd3_v9iYspvoUUXLo5803wOs1-8FQ9uUPKjZlQC5lNGeYvK0-blDdAnpYTPD16eAxsXqbzGYJR4xNseYUkI_IoAwm4MeUw9T225TrwTE3IcRa0KOvWxRTxO2JffNnZGr2JiDnx-zDCdhq76vZ-Yi_Hq6ZTYq-1PKme-VMKPD21C-7Xx_v1ref8f33T19ub-6xZVpW3CtOidPO6pEyKQxdSSqklMwRrUY6AVVMEysNB8EcVSCmqe8nC6OTXCnGL7sPR-6c08MCpQ47Xyy09yKkpQwNKJXqG7tJr49Sm1MpGdwwZ78z-WmgZDgkNjwnNhwTa473J_gy7mD6r3-OiP8DDS2ZDw</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Abumuaileq, Rami Riziq-Yousef</creator><creator>Abu-Assi, Emad</creator><creator>Raposeiras-Roubin, Sergio</creator><creator>López-López, Andrea</creator><creator>Redondo-Diéguez, Alfredo</creator><creator>Álvarez-Iglesias, Diego</creator><creator>Rodríguez-Mañero, Moisés</creator><creator>Peña-Gil, Carlos</creator><creator>González-Juanatey, Jose Ramón</creator><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></search><sort><creationdate>20150501</creationdate><title>Evaluation of SAMe-TT2R2 risk score for predicting the quality of anticoagulation control in a real-world cohort of patients with non-valvular atrial fibrillation on vitamin-K antagonists</title><author>Abumuaileq, Rami Riziq-Yousef ; Abu-Assi, Emad ; Raposeiras-Roubin, Sergio ; López-López, Andrea ; Redondo-Diéguez, Alfredo ; Álvarez-Iglesias, Diego ; Rodríguez-Mañero, Moisés ; Peña-Gil, Carlos ; González-Juanatey, Jose Ramón</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c297t-48310f9fc9b1275a167157772f098b1de18290c7a3e52f18e5dd44dcebf738823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anticoagulants - adverse effects</topic><topic>Anticoagulants - therapeutic use</topic><topic>Atrial Fibrillation - blood</topic><topic>Atrial Fibrillation - diagnosis</topic><topic>Atrial Fibrillation - drug therapy</topic><topic>Atrial Fibrillation - mortality</topic><topic>Blood Coagulation - drug effects</topic><topic>Decision Support Techniques</topic><topic>Drug Monitoring - methods</topic><topic>Female</topic><topic>Hemorrhage - chemically induced</topic><topic>Humans</topic><topic>International Normalized Ratio</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Patient Selection</topic><topic>Predictive Value of Tests</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Stroke - blood</topic><topic>Stroke - diagnosis</topic><topic>Stroke - mortality</topic><topic>Stroke - prevention & control</topic><topic>Thromboembolism - blood</topic><topic>Thromboembolism - diagnosis</topic><topic>Thromboembolism - mortality</topic><topic>Thromboembolism - prevention & control</topic><topic>Treatment Outcome</topic><topic>Vitamin K - antagonists & inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abumuaileq, Rami Riziq-Yousef</creatorcontrib><creatorcontrib>Abu-Assi, Emad</creatorcontrib><creatorcontrib>Raposeiras-Roubin, Sergio</creatorcontrib><creatorcontrib>López-López, Andrea</creatorcontrib><creatorcontrib>Redondo-Diéguez, Alfredo</creatorcontrib><creatorcontrib>Álvarez-Iglesias, Diego</creatorcontrib><creatorcontrib>Rodríguez-Mañero, Moisés</creatorcontrib><creatorcontrib>Peña-Gil, Carlos</creatorcontrib><creatorcontrib>González-Juanatey, Jose Ramón</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><jtitle>Europace (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abumuaileq, Rami Riziq-Yousef</au><au>Abu-Assi, Emad</au><au>Raposeiras-Roubin, Sergio</au><au>López-López, Andrea</au><au>Redondo-Diéguez, Alfredo</au><au>Álvarez-Iglesias, Diego</au><au>Rodríguez-Mañero, Moisés</au><au>Peña-Gil, Carlos</au><au>González-Juanatey, Jose Ramón</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of SAMe-TT2R2 risk score for predicting the quality of anticoagulation control in a real-world cohort of patients with non-valvular atrial fibrillation on vitamin-K antagonists</atitle><jtitle>Europace (London, England)</jtitle><addtitle>Europace</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>17</volume><issue>5</issue><spage>711</spage><epage>717</epage><pages>711-717</pages><issn>1099-5129</issn><eissn>1532-2092</eissn><abstract>Clinicians need to get better at identifying patients who would have poor quality of anticoagulation control with vitamin-K antagonists (VKAs). We assessed the predictive ability of SAMe-TT2R2 score, recently conceived for the prior purpose, and examined its relationship with major bleeding, thromboembolic (TE) complications, and death.
Retrospectively, 911 consecutive patients with non-valvular atrial fibrillation (NVAF) started on VKAs within 8 months were studied. The percentage of international normalized ratios in therapeutic range (PINRR) at different levels was used as a metric of anticoagulation quality. We also tested the SAMe-TT2R2 predictability for major bleeding, TE complications, and death throughout 10 ± 3 months. The PINRR decreased from 62% at zero point to 53% at ≥4 points of SAMe-TT2R2. 82.1% of patients who achieved PINRR ≥ 70% had 0 or 1 point of SAMe-TT2R2. SAMe-TT2R2 performed significantly better at PINRR 70% than at 65 and 60% (c-statistic = 0.60 vs. c-statistic = 0.56). The calibration of SAMe-TT2R2 was excellent (Hosmer-Lemeshow test P-values ≥ 0.6). SAMe-TT2R2 showed significant association with the composite outcome of major bleeding, TE complications, and death [n = 98; hazard ratio (HR) = 1.32; 95% confidence interval (CI) 1.08-1.60]; the c-statistic was 0.57 (95% CI: 0.51-0.62) and P = 0.03. As individual outcomes, SAMe-TT2R2 was significantly associated with death (n = 60; HR = 1.3; 95% CI: 1.03-1.69), but not with either major bleeding (n = 30; HR = 1.2; 95% CI: 0.85-1.76) or TE complications (n = 15; HR = 1.01; 95% CI: 0.58-1.77).
Among NVAF patients, SAMe-TT2R2 could represent a useful clinical tool to identify patients who would have poor quality of anticoagulation control with VKAs. SAMe-TT2R2 successfully predicts the composite outcome of major bleeding, TE complications, and death.</abstract><cop>England</cop><pmid>25662984</pmid><doi>10.1093/europace/euu353</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Anticoagulants - adverse effects Anticoagulants - therapeutic use Atrial Fibrillation - blood Atrial Fibrillation - diagnosis Atrial Fibrillation - drug therapy Atrial Fibrillation - mortality Blood Coagulation - drug effects Decision Support Techniques Drug Monitoring - methods Female Hemorrhage - chemically induced Humans International Normalized Ratio Male Middle Aged Patient Selection Predictive Value of Tests Retrospective Studies Risk Assessment Risk Factors Stroke - blood Stroke - diagnosis Stroke - mortality Stroke - prevention & control Thromboembolism - blood Thromboembolism - diagnosis Thromboembolism - mortality Thromboembolism - prevention & control Treatment Outcome Vitamin K - antagonists & inhibitors |
title | Evaluation of SAMe-TT2R2 risk score for predicting the quality of anticoagulation control in a real-world cohort of patients with non-valvular atrial fibrillation on vitamin-K antagonists |
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