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Influence of Kidney Transplant Status on Warfarin Dose, Anticoagulation Control, and Risk of Hemorrhage.
Yanik, Megan V; Irvin, Marguerite R; Beasley, T Mark; Jacobson, Pamala A; Julian, Bruce A; Limdi, Nita A.
Affiliation
  • Yanik MV; Division of Nephrology, Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
  • Irvin MR; Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama.
  • Beasley TM; Biostatistics, Section on Statistical Genetics, University of Alabama at Birmingham, Birmingham, Alabama.
  • Jacobson PA; Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota.
  • Julian BA; Division of Nephrology, Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
  • Limdi NA; Neurology, University of Alabama at Birmingham, Birmingham, Alabama.
Pharmacotherapy ; 37(11): 1366-1373, 2017 Nov.
Article in En | MEDLINE | ID: mdl-28949423
ABSTRACT
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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Warfarin / Kidney Transplantation / Hemorrhage / Anticoagulants Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Pharmacotherapy Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Warfarin / Kidney Transplantation / Hemorrhage / Anticoagulants Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Pharmacotherapy Year: 2017 Document type: Article