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Use of rivaroxaban attenuates renal function impairment in patients with atrial fibrillation: insights of the EMIR study

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AbstractBackgroundIn atrial fibrillation (AF) patients on vitamin K antagonists, a progressive deterioration of renal function is common but there is limited evidence with long‐term use of rivaroxaban. Herein, we investigated the change in renal function in AF patients after 2 years of rivaroxaban treatment.MethodsThe EMIR registry is an observational and multicentre study including AF patients treated with rivaroxaban for at least 6 months prior to inclusion. Changes in analytical parameters were recorded during 2 years of follow‐up. Renal function was estimated using the Cockroft‐Gault equation.Results1433 patients (638, 44.5% women, mean age of 74.2 ± 9.7 years) were included. Creatinine clearance (CrCl) was available at baseline and at 2 years in 1085 patients. At inclusion, 33.2% of patients had impaired renal function (CrCl <60 ml/min). At 2 years, we were not able to find changes in the proportion of patients with impaired renal function, which increased to 34.6% (p = 0.290). However, the baseline mean CrCl was 76.0 ± 30.5 ml/min and slightly improved at 2 years (77.0 ± 31.8 ml/min; p = 0.014). Overall, the proportion of patients with CrCl <60 ml/min at baseline that had CrCl ≥60 ml/min at 2 years was significantly higher compared to that of patients with CrCl ≥60 ml/min at baseline and CrCl <60 ml/min after (22.2% vs. 13.1%; p < 0.001)ConclusionsIn AF patients on long‐term rivaroxaban therapy, a decrease in renal function was not observed. We even observed a slight improvement in the patients with renal impairment. These results reinforce the idea that rivaroxaban may be a safe option even in patients with renal impairment.
Title: Use of rivaroxaban attenuates renal function impairment in patients with atrial fibrillation: insights of the EMIR study
Description:
AbstractBackgroundIn atrial fibrillation (AF) patients on vitamin K antagonists, a progressive deterioration of renal function is common but there is limited evidence with long‐term use of rivaroxaban.
Herein, we investigated the change in renal function in AF patients after 2 years of rivaroxaban treatment.
MethodsThe EMIR registry is an observational and multicentre study including AF patients treated with rivaroxaban for at least 6 months prior to inclusion.
Changes in analytical parameters were recorded during 2 years of follow‐up.
Renal function was estimated using the Cockroft‐Gault equation.
Results1433 patients (638, 44.
5% women, mean age of 74.
2 ± 9.
7 years) were included.
Creatinine clearance (CrCl) was available at baseline and at 2 years in 1085 patients.
At inclusion, 33.
2% of patients had impaired renal function (CrCl <60 ml/min).
At 2 years, we were not able to find changes in the proportion of patients with impaired renal function, which increased to 34.
6% (p = 0.
290).
However, the baseline mean CrCl was 76.
0 ± 30.
5 ml/min and slightly improved at 2 years (77.
0 ± 31.
8 ml/min; p = 0.
014).
Overall, the proportion of patients with CrCl <60 ml/min at baseline that had CrCl ≥60 ml/min at 2 years was significantly higher compared to that of patients with CrCl ≥60 ml/min at baseline and CrCl <60 ml/min after (22.
2% vs.
13.
1%; p < 0.
001)ConclusionsIn AF patients on long‐term rivaroxaban therapy, a decrease in renal function was not observed.
We even observed a slight improvement in the patients with renal impairment.
These results reinforce the idea that rivaroxaban may be a safe option even in patients with renal impairment.

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