Key result
Kidney transplant recipients on warfarin face ~2.1-fold higher risk of major hemorrhage.
Why the study?
This study assessed whether warfarin dose requirement, anticoagulation control, and risk of hemorrhage differ in kidney transplant recipients compared with patients without kidney transplants.
Does kidney transplant status affect warfarin dose requirement, anticoagulation control, and risk of hemorrhage in adults starting warfarin?
Cohort (n=1,695)
Yes
Does kidney transplant status affect warfarin dose requirement, anticoagulation control, and risk of hemorrhage in adults starting warfarin?
Kidney transplant recipients initiating warfarin require approximately 20% lower doses than non-recipients to achieve similar anticoagulation control.
Answers are grounded in this paper and cite their sources.
Suggests conservative initial warfarin dosing may be prudent in kidney transplant recipients; leaves open whether.
Study Design To assess whether warfarin dose requirement, anticoagulation control, and risk of hemorrhage differ in kidney transplant recipients (KTRs) compared with patients without kidney transplants (non‐KTRs). Design Analysis of data from the Warfarin Pharmacogenetics Cohort, a prospective cohort of first‐time warfarin users followed at two anticoagulation clinics. Setting Two outpatient anticoagulation clinics at two large, academic, tertiary care hospitals. Patients Adults aged 20 years or older starting warfarin for anticoagulation with a therapeutic international normalized ratio (INR) goal of 2–3 who were KTRs (n=65) or non‐KTRs (n=1630). Measurements and Main Results Warfarin dose requirement, anticoagulation control, and risk of hemorrhage were assessed in each group. KTRs required an approximately 20% lower warfarin dose (4.7 vs 5.6 mg/day, p=0.0005) compared with non‐KTRs. Genetic variants had similar effects on dose in both groups. Mean percentage of time in therapeutic range (PTTR) was similar among KTRs and non‐KTRs. Although the proportion of patients achieving good anticoagulation control (PTTR ≥ 60%) was low in both groups, it was similar among KTRs and non‐KTRs. KTRs had a higher risk of major hemorrhage (hazard ratio 2.1, p=0.0081), but this difference was not statistically significant after controlling for kidney function, clinical, and genetic factors. Conclusion KTRs initiating warfarin require lower doses and closer monitoring to optimize anticoagulation therapy. Additional studies are needed to confirm these findings.
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Yanik et al. (2017) conducted a cohort in First-time warfarin users requiring anticoagulation (n=1,695). Kidney transplant recipient status vs. Patients without kidney transplants (non-KTRs) was evaluated on Warfarin dose requirement, anticoagulation control, and risk of major hemorrhage (HR 2.1, p=0.0081). Kidney transplant recipients required a ~20% lower warfarin dose than non-recipients (4.7 vs 5.6 mg/day, p=0.0005) and had a higher unadjusted risk of major hemorrhage (HR 2.1, p=0.0081).
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