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SAMe-TT(2)R(2) Score in the Outpatient Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse Events
BACKGROUND: The SAMe-TT(2)R(2) score was developed to predict which patients on oral anticoagulation with vitamin K antagonists (VKAs) will reach an adequate time in therapeutic range (TTR) (> 65%-70%). Studies have reported a relationship between this score and the occurrence of adverse events....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia - SBC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421467/ https://www.ncbi.nlm.nih.gov/pubmed/28538758 http://dx.doi.org/10.5935/abc.20170052 |
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author | Pivatto Júnior, Fernando Scheffel, Rafael Selbach Ries, Lucas Wolkind, Ricardo Roitman Marobin, Roberta Barkan, Sabrina Sigal Amon, Luís Carlos Biolo, Andréia |
author_facet | Pivatto Júnior, Fernando Scheffel, Rafael Selbach Ries, Lucas Wolkind, Ricardo Roitman Marobin, Roberta Barkan, Sabrina Sigal Amon, Luís Carlos Biolo, Andréia |
author_sort | Pivatto Júnior, Fernando |
collection | PubMed |
description | BACKGROUND: The SAMe-TT(2)R(2) score was developed to predict which patients on oral anticoagulation with vitamin K antagonists (VKAs) will reach an adequate time in therapeutic range (TTR) (> 65%-70%). Studies have reported a relationship between this score and the occurrence of adverse events. OBJECTIVE: To describe the TTR according to the score, in addition to relating the score obtained with the occurrence of adverse events in patients with nonvalvular atrial fibrillation (AF) on oral anticoagulation with VKAs. METHODS: Retrospective cohort study including patients with nonvalvular AF attending an outpatient anticoagulation clinic of a tertiary hospital. Visits to the outpatient clinic and emergency, as well as hospital admissions to the institution, during 2014 were evaluated. The TTR was calculated through the Rosendaal´s method. RESULTS: We analyzed 263 patients (median TTR, 62.5%). The low-risk group (score 0-1) had a better median TTR as compared with the high-risk group (score ≥ 2): 69.2% vs. 56.3%, p = 0.002. Similarly, the percentage of patients with TTR ≥ 60%, 65% or 70% was higher in the low-risk group (p < 0.001, p = 0.001 and p = 0.003, respectively). The high-risk group had a higher percentage of adverse events (11.2% vs. 7.2%), although not significant (p = 0.369). CONCLUSIONS: The SAMe-TT(2)R(2) score proved to be effective to predict patients with a better TTR, but was not associated with adverse events. |
format | Online Article Text |
id | pubmed-5421467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Sociedade Brasileira de Cardiologia - SBC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54214672017-05-11 SAMe-TT(2)R(2) Score in the Outpatient Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse Events Pivatto Júnior, Fernando Scheffel, Rafael Selbach Ries, Lucas Wolkind, Ricardo Roitman Marobin, Roberta Barkan, Sabrina Sigal Amon, Luís Carlos Biolo, Andréia Arq Bras Cardiol Original Articles BACKGROUND: The SAMe-TT(2)R(2) score was developed to predict which patients on oral anticoagulation with vitamin K antagonists (VKAs) will reach an adequate time in therapeutic range (TTR) (> 65%-70%). Studies have reported a relationship between this score and the occurrence of adverse events. OBJECTIVE: To describe the TTR according to the score, in addition to relating the score obtained with the occurrence of adverse events in patients with nonvalvular atrial fibrillation (AF) on oral anticoagulation with VKAs. METHODS: Retrospective cohort study including patients with nonvalvular AF attending an outpatient anticoagulation clinic of a tertiary hospital. Visits to the outpatient clinic and emergency, as well as hospital admissions to the institution, during 2014 were evaluated. The TTR was calculated through the Rosendaal´s method. RESULTS: We analyzed 263 patients (median TTR, 62.5%). The low-risk group (score 0-1) had a better median TTR as compared with the high-risk group (score ≥ 2): 69.2% vs. 56.3%, p = 0.002. Similarly, the percentage of patients with TTR ≥ 60%, 65% or 70% was higher in the low-risk group (p < 0.001, p = 0.001 and p = 0.003, respectively). The high-risk group had a higher percentage of adverse events (11.2% vs. 7.2%), although not significant (p = 0.369). CONCLUSIONS: The SAMe-TT(2)R(2) score proved to be effective to predict patients with a better TTR, but was not associated with adverse events. Sociedade Brasileira de Cardiologia - SBC 2017-04 /pmc/articles/PMC5421467/ /pubmed/28538758 http://dx.doi.org/10.5935/abc.20170052 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Pivatto Júnior, Fernando Scheffel, Rafael Selbach Ries, Lucas Wolkind, Ricardo Roitman Marobin, Roberta Barkan, Sabrina Sigal Amon, Luís Carlos Biolo, Andréia SAMe-TT(2)R(2) Score in the Outpatient Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse Events |
title | SAMe-TT(2)R(2) Score in the Outpatient
Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse
Events |
title_full | SAMe-TT(2)R(2) Score in the Outpatient
Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse
Events |
title_fullStr | SAMe-TT(2)R(2) Score in the Outpatient
Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse
Events |
title_full_unstemmed | SAMe-TT(2)R(2) Score in the Outpatient
Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse
Events |
title_short | SAMe-TT(2)R(2) Score in the Outpatient
Anticoagulation Clinic to Predict Time in Therapeutic Range and Adverse
Events |
title_sort | same-tt(2)r(2) score in the outpatient
anticoagulation clinic to predict time in therapeutic range and adverse
events |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421467/ https://www.ncbi.nlm.nih.gov/pubmed/28538758 http://dx.doi.org/10.5935/abc.20170052 |
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