Uwe Aickelin

Work place: Department of Computer Science, University of Nottingham, UK

E-mail: uwe.aickelin@nottingham.ac.uk

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Research Interests: Computational Science and Engineering, Artificial Intelligence, Data Structures and Algorithms, Algorithmic Complexity Theory

Biography

Uwe Aickelin is EPSRC Advanced Research Fellow and Professor of Computer Science at the University of Nottingham, where he leads one of its four research groups: Intelligent Modelling & Analysis (IMA). His long-term research vision is to create an integrated framework of problem understanding, modelling and analysis techniques, based on an inter-disciplinary perspective of their closely-coupled nature. A summary of his current research interests is Modelling, Artificial Intelligence and Complexity Science for Data Analysis.

Author Articles
Feature Selection in Detection of Adverse Drug Reactions from the Health Improvement Network (THIN) Database

By Yihui Liu Uwe Aickelin

DOI: https://doi.org/10.5815/ijitcs.2015.03.10, Pub. Date: 8 Feb. 2015

Adverse drug reaction (ADR) is widely concerned for public health issue. ADRs are one of most common causes to withdraw some drugs from market. Prescription event monitoring (PEM) is an important approach to detect the adverse drug reactions. The main problem to deal with this method is how to automatically extract the medical events or side effects from high-throughput medical events, which are collected from day to day clinical practice. In this study we propose a novel concept of feature matrix to detect the ADRs. Feature matrix, which is extracted from big medical data from The Health Improvement Network (THIN) database, is created to characterize the medical events for the patients who take drugs. Feature matrix builds the foundation for the irregular and big medical data. Then feature selection methods are performed on feature matrix to detect the significant features. Finally the ADRs can be located based on the significant features. The experiments are carried out on three drugs: Atorvastatin, Alendronate, and Metoclopramide. Major side effects for each drug are detected and better performance is achieved compared to other computerized methods. The detected ADRs are based on computerized methods, further investigation is needed.

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