A fuzzy logic-based computational recognition-primed decision model

被引:43
作者
Ji, Yanqing
Massanari, R. Michael
Ager, Joel
Yen, John
Miller, Richard E.
Ying, Hao
机构
[1] Wayne State Univ, Dept Elect & Comp Engn, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Internal Med, Detroit, MI 48202 USA
[3] Wayne State Univ, Ctr Healthcare Effecyiveness Res, Detroit, MI 48202 USA
[4] Wayne State Univ, Dept Family Med & Publ Hlth Sci, Detroit, MI USA
[5] Wayne State Univ, Div Biostat & Epidemiol, Detroit, MI USA
[6] Penn State Univ, Coll Informat Sci & Technol, University Pk, PA 16802 USA
[7] Vet Affairs Med Ctr, Detroit, MI USA
关键词
medical decision-making; Naturalistic decision-making; Recognition-primed decision model; Computational recognition-primed decision model; Experience-based reasoning; Adverse drug reactions; fuzzy logic; Similarity measure;
D O I
10.1016/j.ins.2007.02.026
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
The recognition-primed decision (RPD) model is a primary naturalistic decision-making approach which seeks to explicitly recognize how human decision makers handle complex tasks and environment based on their experience. Motivated by the need for quantitative computer modeling and simulation of human decision processes in various application domains, including medicine, we have developed a general-purpose computational fuzzy RPD model that utilizes fuzzy sets, fuzzy rules, and fuzzy reasoning to represent, interpret, and compute imprecise and subjective information in every aspect of the model. Experiences acquired by solicitation with experts are stored in experience knowledge bases. New local and global similarity measures have been developed to identify the experience that is most applicable to the current situation in a specific decision-making context. Furthermore, an action evaluation strategy has been developed to select the workable course of action. The proposed fuzzy RPD model has been preliminarily validated by using it to calculate the extent of causality between a drug (Cisapride, withdrawn by the FDA from the market in 2000) and some of its adverse effects for 100 hypothetical patients. The simulated patients were created based on the profiles of over 1000 actual patients treated with the drug at our medical center before its withdrawal. The model validity was demonstrated by comparing the decisions made by the proposed model and those by two independent internists. The levels of agreement were established by the weighted Kappa statistic and the results suggested good to excellent agreement. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:4338 / 4353
页数:16
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