Revisiting Warfarin Dosing Using Machine Learning Techniques

Author:

Sharabiani Ashkan1,Bress Adam2,Douzali Elnaz1,Darabi Houshang3

Affiliation:

1. Department of Mechanical and Industrial Engineering, University of Illinois at Chicago, Room 4209, SEL West Building, 950 South Halsted Street, Chicago, IL 60607, USA

2. Department of Pharmacotherapy, University of Utah, 30 South 2000 East, Room 4929, Salt Lake City, UT 84112, USA

3. Department of Mechanical and Industrial Engineering, University of Illinois at Chicago, Room 2055, ERF Building, 842 W Taylor Street, Chicago, IL 60607, USA

Abstract

Determining the appropriate dosage of warfarin is an important yet challenging task. Several prediction models have been proposed to estimate a therapeutic dose for patients. The models are either clinical models which contain clinical and demographic variables or pharmacogenetic models which additionally contain the genetic variables. In this paper, a new methodology for warfarin dosing is proposed. The patients are initially classified into two classes. The first class contains patients who require doses of >30 mg/wk and the second class contains patients who require doses of ≤30 mg/wk. This phase is performed using relevance vector machines. In the second phase, the optimal dose for each patient is predicted by two clinical regression models that are customized for each class of patients. The prediction accuracy of the model was 11.6 in terms of root mean squared error (RMSE) and 8.4 in terms of mean absolute error (MAE). This was 15% and 5% lower than IWPC and Gage models (which are the most widely used models in practice), respectively, in terms of RMSE. In addition, the proposed model was compared with fixed-dose approach of 35 mg/wk, and the model proposed by Sharabiani et al. and its outperformance were proved in terms of both MAE and RMSE.

Funder

University of Illinois at Chicago

Publisher

Hindawi Limited

Subject

Applied Mathematics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Modeling and Simulation,General Medicine

Reference36 articles.

1. American Heart Association/American College of Cardiology Foundation guide to warfarin therapy11The American Heart Association makes every effort to avoid any actual or potential conflicts of interest that may arise as a result of an outside relationship or a personal, professional, or business interest of a member of the writing panel. Specifically, all members of the writing group are required to complete and submit a Disclosure Questionnaire showing all such relationships that might be perceived as real or potential conflicts of interest.This statement has been co-published in the April 1, 2003, issue of Circulation.This statement was approved by the American Heart Association Science Advisory and Coordinating Committee in October 2002 and by the American College of Cardiology Board of Trustees in February 2003. A single reprint is available by calling 800-242-8721 (US only) or writing the American Heart Association, Public Information, 7272 Greenville Ave, Dallas, TX 75231-4596. Ask for reprint No. 71-0254. To purchase additional reprints: up to 999 copies, call 800-611-6083 (US only) or fax 413-665-2671; 1000 or more copies, call 410-528-4426, fax 410-528-4264, or e-mail klbradle@lww.com. To make photocopies for personal or educational use, call the Copyright Clearance Center, 978-750-8400.

2. Major Hemorrhage and Tolerability of Warfarin in the First Year of Therapy Among Elderly Patients With Atrial Fibrillation

3. Effect of Intensity of Oral Anticoagulation on Stroke Severity and Mortality in Atrial Fibrillation

4. Use of Pharmacogenetic and Clinical Factors to Predict the Therapeutic Dose of Warfarin

5. Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data

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