DocumentCode :
1479493
Title :
A Potential Causal Association Mining Algorithm for Screening Adverse Drug Reactions in Postmarketing Surveillance
Author :
Ji, Yanqing ; Ying, Hao ; Dews, Peter ; Mansour, Ayman ; Tran, John ; Miller, Richard E. ; Massanari, R. Michael
Author_Institution :
Dept. of Electr. & Comput. Eng., Gonzaga Univ., Spokane, WA, USA
Volume :
15
Issue :
3
fYear :
2011
fDate :
5/1/2011 12:00:00 AM
Firstpage :
428
Lastpage :
437
Abstract :
Early detection of unknown adverse drug reactions (ADRs) in postmarketing surveillance saves lives and prevents harmful consequences. We propose a novel data mining approach to signaling potential ADRs from electronic health databases. More specifically, we introduce potential causal association rules (PCARs) to represent the potential causal relationship between a drug and ICD-9 (CDC. (2010). International Classification of Diseases, Ninth Revision (ICD-9). [Online]. Available: http://www.cdc.gov/nchs/icd/icd9.html) coded signs or symptoms representing potential ADRs. Due to the infrequent nature of ADRs, the existing frequency-based data mining methods cannot effectively discover PCARs. We introduce a new interestingness measure, potential causal leverage, to quantify the degree of association of a PCAR. This measure is based on the computational, experience-based fuzzy recognition-primed decision (RPD) model that we developed previously (Y. Ji, R. M. Massanari, J. Ager, J. Yen, R. E. Miller, and H. Ying, “A fuzzy logic-based computational recognition-primed decision model,” Inf. Sci., vol. 177, pp. 4338-4353, 2007) on the basis of the well-known, psychology-originated qualitative RPD model (G. A. Klein, “A recognition-primed decision making model of rapid decision making,” in Decision Making in Action: Models and Methods, 1993, pp. 138-147). The potential causal leverage assesses the strength of the association of a drug-symptom pair given a collection of patient cases. To test our data mining approach, we retrieved electronic medical data for 16 206 patients treated by one or more than eight drugs of our interest at the Veterans Affairs Medical Center in Detroit between 2007 and 2009. We selected enalapril as the target drug for this ADR signal generation study. We used our algorithm to preliminarily evaluate the associations between enalapril and all the ICD-9 codes associated with it. The experimental results indicate that our - pproach has a potential to better signal potential ADRs than risk ratio and leverage, two traditional frequency-based measures. Among the top 50 signal pairs (i.e., enalapril versus symptoms) ranked by the potential causal-leverage measure, the physicians on the project determined that eight of them probably represent true causal associations.
Keywords :
biochemistry; causality; data mining; drugs; medical information systems; surveillance; ICD-9; International Classification of Diseases; Veterans Affairs Medical Center Detroit; adverse drug reaction screening; data mining approach; drug-symptom pair; electronic health databases; electronic medical data; enalapril; experience-based fuzzy recognition-primed decision; harmful consequences; interestingness measure; postmarketing surveillance; potential causal association mining algorithm; potential causal association rules; psychology-originated qualitative RPD model; unknown adverse drug reactions; Association rules; Computational modeling; Databases; Drugs; Electric potential; Frequency measurement; Adverse drug reactions (ADRs); data mining; fuzzy logic; postmarketing surveillance; potential causal association rules (PCARs); recognition-primed decision model (RPD); Algorithms; Data Mining; Databases, Factual; Drug Toxicity; Electronic Health Records; Enalapril; Fuzzy Logic; Humans; Pattern Recognition, Automated; Product Surveillance, Postmarketing; Signal Processing, Computer-Assisted;
fLanguage :
English
Journal_Title :
Information Technology in Biomedicine, IEEE Transactions on
Publisher :
ieee
ISSN :
1089-7771
Type :
jour
DOI :
10.1109/TITB.2011.2131669
Filename :
5738341
Link To Document :
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