Key result
Acute kidney injury during vitamin K antagonist therapy was associated with significantly higher median INR compared to a reference time point with stable kidney function (3.17 vs 2.24; P<0.0001).
Why the study?
Case reports suggest acute kidney injury may cause derailment of VKA therapy, but its effect on anticoagulation has not been systematically described.
Does acute kidney injury increase the risk of overanticoagulation in patients treated with vitamin K antagonists?
Observational (n=100)
No
Does acute kidney injury increase the risk of overanticoagulation in patients treated with vitamin K antagonists?
Acute kidney injury in patients on vitamin K antagonists is associated with a significant increase in INR and risk of overanticoagulation, necessitating close monitoring.
BACKGROUND: Vitamin K antagonists (VKAs) are still in use for oral anticoagulation, but not all indications allow their replacement by direct oral anticoagulants. Although formal dose reduction is not required in patients with impaired kidney function, case reports indicate that acute kidney injury (AKI) might be associated with derailment of VKA therapy. METHODS: The study retrospectively collected patients from a tertiary nephrology care centre who experienced AKI while being treated with VKA. In these individuals, the international normalized ratio (INR) as a measure of anticoagulant effect during renal failure was compared with a reference time point with stable kidney function. RESULTS: A total of 100 patients with AKI and ongoing VKA therapy met the inclusion criteria. The majority (76%) of patients had AKI with CKD. Volume depletion (n = 43), septic renal failure (n = 22), decompensated heart failure (n = 18) and toxic renal damage (n = 11) were the most important causes of AKI. The average INR values at the time of AKI were higher than at the reference time point [median 3.17 (range 1.10-13.0) versus 2.24 (1.07-5.17); P < 0.0001]. Fifty-four patients had INR values above the recommended therapeutic range for their indication at the time point of AKI. Bleeding complications occurred in 24 patients during AKI and the VKA dose had to be reduced in 55. Women, patients with low body mass index and patients with diabetes were predisposed to overanticoagulation during AKI. CONCLUSIONS: The effect of AKI on anticoagulation by VKA has not been systematically described. This risk should be considered in patients at high risk for AKI.
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Süfling et al. (2021) conducted an observational in Acute kidney injury during vitamin K antagonist therapy (n=100). Acute kidney injury vs. Stable kidney function (reference time point) was evaluated on International normalized ratio (INR) (p=<0.0001). Acute kidney injury during vitamin K antagonist therapy was associated with significantly higher median INR compared to a reference time point with stable kidney function (3.17 vs 2.24; P<0.0001).
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