What is the role for population pharmacokinetics in hemophilia?

Author:

Iorio Alfonso12,McEneny-King Alanna3,Keepanasseril Arun1,Foster Gary14,Edginton Andrea3

Affiliation:

1. Department of Clinical Epidemiology and Biostatistic, McMaster University, 1280 Main St West, Hamilton, ON L8S 4K1, Canada

2. Department of Medicine, Hamilton-Niagara Regional Hemophilia Treatment Centre, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4K1, Canada

3. School of Pharmacy, University of Waterloo, 200 University Avenue West, Waterloo, ON N2L 3G1, Canada

4. Biostatistics Unit, St. Joseph’s Healthcare, 50 Charlton Avenue East, Hamilton, ON L8N 4A6, Canada

Abstract

Prevention of bleeding in hemophilia requires that plasma levels of the deficient factor exceed the desired minimum target level. Large interindividual variability suggests that knowledge of individual pharmacokinetic (PK) would help to achieve this goal, simultaneously minimizing infusion frequency and the amount of concentrate used. Population PK (PopPK) allows for the incorporation of determinants of interpatient variability and eliminates the need for extensive postinfusion plasma sampling. Barriers to implementation of PopPK are the need for concentrate specific models, Bayesian calculation power, specific expertise for validation and appraisal of forecasted estimates. The Web Accessible Population Pharmacokinetic Service – Hemophilia ( www.wapps-hemo.org ), developed by an international research network of hemophilia centers will test if PK-guided dose individualization can improve patient important outcomes in hemophilia.

Publisher

Future Science Ltd

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