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Estimation and prediction system for multi‐state disease process: application to analysis of organized screening regime
Author(s) -
Chang ChiMing,
Lin WenChou,
Kuo HsuSung,
Yen MingFang,
Chen Tony HsiuHsi
Publication year - 2007
Publication title -
journal of evaluation in clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.737
H-Index - 73
eISSN - 1365-2753
pISSN - 1356-1294
DOI - 10.1111/j.1365-2753.2006.00765.x
Subject(s) - computer science , estimation , process (computing) , software , estimation theory , outcome (game theory) , hazard , data mining , machine learning , statistics , algorithm , mathematics , engineering , chemistry , systems engineering , mathematical economics , organic chemistry , programming language , operating system
Rationale, aims and objectives The disease progression of cancer and non‐malignant chronic disease often involve a multi‐state transition. However, estimation of parameters and prediction regarding the multi‐state disease process are complex. This study aimed to develop an estimation and prediction system with a computer‐assisted software using SAS/SCL as a platform to predict the risk of any outcome arising from the underlying multi‐state process with or without the incorporation of individual characteristics. Method The computer‐aided system is first constructed following the theoretical framework of stochastic process. The functions provided in this software include model specification, formulation of likelihood function, parameter estimation, model validation and model prediction. An example of breast cancer screening for a high‐risk group in Taiwan was used to demonstrate the usefulness of this software. Results The natural history of breast cancer of a three‐state disease process has been demonstrated. Two suspected risk factors, late age at first full‐term pregnancy and obesity, were considered by the form of the proportional hazard model. Formulation of intensity matrix, likelihood function, assignment of initial values, and parameter constraint and estimation were successfully demonstrated in model specification. Model validation suggested a good fit of the constructed model. The application of model prediction enables one to project the effectiveness of organized screening by different inter‐screening intervals from a policy level or from an individual basis. Conclusions A computer‐aided estimation and prediction system for multi‐state disease process was developed and demonstrated. This system can be applied to data with the property of multi‐state transitions in association with events or disease.