Modeling good research practices--overview: a report of the ISPOR-SMDM Modeling Good Research Practices Task Force--1
J Jaime Caro, Andrew H Briggs, Uwe Siebert, Karen M Kuntz, ISPOR-SMDM Modeling Good Research Practices Task Force, J Jaime Caro, Andrew H Briggs, Uwe Siebert, Karen M Kuntz, ISPOR-SMDM Modeling Good Research Practices Task Force
Abstract
Models--mathematical frameworks that facilitate estimation of the consequences of health care decisions--have become essential tools for health technology assessment. Evolution of the methods since the first ISPOR Modeling Task Force reported in 2003 has led to a new Task Force, jointly convened with the Society for Medical Decision Making, and this series of seven articles presents the updated recommendations for best practices in conceptualizing models; implementing state-transition approaches, discrete event simulations, or dynamic transmission models; and dealing with uncertainty and validating and reporting models transparently. This overview article introduces the work of the Task Force, provides all the recommendations, and discusses some quandaries that require further elucidation. The audience for these articles includes those who build models, stakeholders who utilize their results, and, indeed, anyone concerned with the use of models to support decision making.
Copyright © 2012 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.
Source: PubMed