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Comparison between CHA(2)DS(2)-VASc and the new R(2)CHADS(2) and ATRIA scores at predicting thromboembolic event in non-anticoagulated and anticoagulated patients with non-valvular atrial fibrillation
BACKGROUND: Accurate risk stratification is considered the first and most important step in the management of patients with non-valvular atrial fibrillation (NVAF). We compared the performance of the widely used CHA(2)DS(2)-VASc and the recently developed R(2)CHADS(2) and ATRIA scores, for predictin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653932/ https://www.ncbi.nlm.nih.gov/pubmed/26584938 http://dx.doi.org/10.1186/s12872-015-0149-3 |
Sumario: | BACKGROUND: Accurate risk stratification is considered the first and most important step in the management of patients with non-valvular atrial fibrillation (NVAF). We compared the performance of the widely used CHA(2)DS(2)-VASc and the recently developed R(2)CHADS(2) and ATRIA scores, for predicting thromboembolic (TE) event in either non-anticoagulated or anticoagulated patients with NVAF. METHODS: The non-anticoagulated cohort was comprised of 154 patients, whereas 911 patients formed the cohort of patients on vitamin-K-antagonist. The scores were computed using the criteria mentioned in their developmental cohorts. Measures of performance for the risk scores were evaluated at predicting TE event. RESULTS: In the non-anticoagulated cohort, 9 TE events occurred during 11 ± 2.7 months. CHA(2)DS(2)-VASc showed significant association with TE occurrence: hazard ratio (HR) = 1.58 (95 % confidence interval [95 % IC] 1.01–2.46), but R(2)CHADS(2) and ATRIA did not (HR = 1.23 (95 % CI 0.86–1.77) and 1.20 (95 % CI 0.93–1.56), respectively. In the anticoagulated cohort, after 10 ± 3 months of follow up, 18 TE events were developed. In that cohort, the three scores showed similar association with TE risk: HR = 1.49 (95 % CI 1.13–1.97), 1.41 (95 % CI 1.13–1.77) and 1.37 (95 % CI 1.12–1.66) for CHA(2)DS(2)-VASc, R(2)CHADS(2) and ATRIA, respectively. In both cohorts, no TE event occurred in patients classified in the low risk category according to CHA(2)DS(2)-VASc or R(2)CHADS(2). CONCLUSIONS: In this study of NVAF patients, CHA(2)DS(2)-VASc has better association with TE events than the new R(2)CHADS(2) and ATRIA risk scores in the non-anticoagulated cohort. CHA(2)DS(2)-VASc and R(2)CHADS(2) can identify patients at truly low risk regardless of the anticoagulation status. |
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