AI Article Synopsis

  • A study was conducted to determine the risk of acute kidney injury (AKI) in elderly atrial fibrillation patients prescribed either direct oral anticoagulants (dabigatran, rivaroxaban, or apixaban) or warfarin.
  • The study involved 20,683 outpatients in Ontario, Canada, where researchers used statistical methods to compare AKI risks linked to each anticoagulant.
  • Results indicated that all direct oral anticoagulants showed a significantly lower risk of AKI compared to warfarin, with findings consistent across different levels of kidney function.

Article Abstract

Background And Objectives: Anticoagulation with either a vitamin K antagonist or a direct oral anticoagulant may be associated with AKI. Our objective was to assess the risk of AKI among elderly individuals with atrial fibrillation newly prescribed a direct oral anticoagulant (dabigatran, rivaroxaban, or apixaban) versus warfarin.

Design, Setting, Participants, & Measurements: Our population-based cohort study included 20,683 outpatients in Ontario, Canada, ≥66 years with atrial fibrillation who were prescribed warfarin, dabigatran, rivaroxaban, or apixaban between 2009 and 2017. Inverse probability of treatment weighting on the basis of derived propensity scores for the treatment with each direct oral anticoagulant was used to balance baseline characteristics among patients receiving each of the three direct oral anticoagulants compared with warfarin. Cox proportional hazards regression was performed in the weighted population to compare the association between the prescribed anticoagulant and the outcomes of interest. The exposure was an outpatient prescription of warfarin or one of the direct oral anticoagulants. The primary outcome was a hospital encounter with AKI, defined using Kidney Disease Improving Global Outcomes thresholds. Prespecified subgroup analyses were conducted by eGFR category and by the percentage of international normalized ratio measurements in range, a validated marker of anticoagulation control.

Results: Each direct oral anticoagulant was associated with a significantly lower risk of AKI compared with warfarin (weighted hazard ratio, 0.65; 95% confidence interval, 0.53 to 0.80 for dabigatran; weighted hazard ratio, 0.85; 95% confidence interval, 0.73 to 0.98 for rivaroxaban; and weighted hazard ratio, 0.81; 95% confidence interval, 0.72 to 0.93 for apixaban). In the subgroup analysis, the lower risk of AKI associated with each direct oral anticoagulant was consistent across each eGFR strata. The risk of AKI was significantly lower among users of each of the direct oral anticoagulants compared with warfarin users who had a percentage of international normalized ratio measurements ≤56%.

Conclusions: Direct oral anticoagulants were associated with a lower risk of AKI compared with warfarin.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8499008PMC
http://dx.doi.org/10.2215/CJN.05920421DOI Listing

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