2015
DOI: 10.1016/j.jval.2015.09.097
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Apixaban In Patients With Atrial Fibrillation: Patient Characteristics Of The Latin America Cohort From A Multinational Clinical Trial

Abstract: A809 1.3% was observed (p< 0.001). For VAS-identified adherent patients, CVR decreased significantly by 4.4% from baseline to 90 days (p< 0.001). However, a significant decrease of 4.3% (p< 0.001) was also observed for VAS-identified non-adherent patients. ConClusions: Patients identified as adherent using the first item of the BAAS showed significantly improved 10-year cardiovascular risk scores after 90 days of treatment with valsartan, compared to patients who were identified as non-adherent. The VAS scale … Show more

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“…These constituted more than Dose reduction edoxaban in NVAF and VTE: 30 mg od where one of CrCl 15-49 mL/min, body weight ≤60kg, concomitant use of cyclosporin, dronedarone, erythromycin or ketoconazole ACS = acute coronary syndrome; bd = twice per day; CrCl = creatinine clearance; LMWH = low molecular weight heparin; NICE = National Institute for Health and Care Excellence; NOAC = non-vitamin K oral anticoagulant; NVAF = non-valvular atrial fibrillation; od = once daily; P-gp = P glycoprotein; T max = time to peak level post ingestion; ULN = upper limit of normal; VTE = venous thromboembolism 25% of the study population in the ARISTOTLE (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation) trial; the efficacy and safety benefits of apixaban were preserved in these patients despite the greater risk of thromboembolic disease and bleeding associated with both apixaban and warfarin. 9 Similar findings were obtained with dabigatran 10 and with rivaroxaban although bleeding was higher in the rivaroxaban arm. 11 In conclusion, NOACs are a reasonable choice of anticoagulant in patients with AF with some forms of valvular disease taking into account the individual drug properties.…”
Section: Patients With Valvular Heart Diseasesupporting
confidence: 65%
“…These constituted more than Dose reduction edoxaban in NVAF and VTE: 30 mg od where one of CrCl 15-49 mL/min, body weight ≤60kg, concomitant use of cyclosporin, dronedarone, erythromycin or ketoconazole ACS = acute coronary syndrome; bd = twice per day; CrCl = creatinine clearance; LMWH = low molecular weight heparin; NICE = National Institute for Health and Care Excellence; NOAC = non-vitamin K oral anticoagulant; NVAF = non-valvular atrial fibrillation; od = once daily; P-gp = P glycoprotein; T max = time to peak level post ingestion; ULN = upper limit of normal; VTE = venous thromboembolism 25% of the study population in the ARISTOTLE (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation) trial; the efficacy and safety benefits of apixaban were preserved in these patients despite the greater risk of thromboembolic disease and bleeding associated with both apixaban and warfarin. 9 Similar findings were obtained with dabigatran 10 and with rivaroxaban although bleeding was higher in the rivaroxaban arm. 11 In conclusion, NOACs are a reasonable choice of anticoagulant in patients with AF with some forms of valvular disease taking into account the individual drug properties.…”
Section: Patients With Valvular Heart Diseasesupporting
confidence: 65%
“…Further subgroup analysis of the Latin American cohort suggests that results in terms of safety and efficacy are consistent with those seen in total study population, with minimal geographic variability within the region. 52 …”
Section: Methodsmentioning
confidence: 99%