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Drug Adverse Event Detection in Health Plan Data Using the Gamma Poisson Shrinker and Comparison to the Tree-based Scan Statistic

Authors :
David Smith
Robert Reynolds
Marsha A. Raebel
Douglas Roblin
Margaret J. Gunter
Lisa Herrinton
Pamala A. Pawloski
Denise Boudreau
Susan E. Andrade
K. Arnold Chan
Taliser R. Avery
Robert L. Davis
Martin Kulldorff
Andrew Bate
Fang Zhang
Inna Dashevsky
Kenneth R. Petronis
Jeffrey S. Brown
Source :
Pharmaceutics, Vol 5, Iss 1, Pp 179-200 (2013)
Publication Year :
2013
Publisher :
MDPI AG, 2013.

Abstract

Background: Drug adverse event (AE) signal detection using the Gamma Poisson Shrinker (GPS) is commonly applied in spontaneous reporting. AE signal detection using large observational health plan databases can expand medication safety surveillance. Methods: Using data from nine health plans, we conducted a pilot study to evaluate the implementation and findings of the GPS approach for two antifungal drugs, terbinafine and itraconazole, and two diabetes drugs, pioglitazone and rosiglitazone. We evaluated 1676 diagnosis codes grouped into 183 different clinical concepts and four levels of granularity. Several signaling thresholds were assessed. GPS results were compared to findings from a companion study using the identical analytic dataset but an alternative statistical method—the tree-based scan statistic (TreeScan). Results: We identified 71 statistical signals across two signaling thresholds and two methods, including closely-related signals of overlapping diagnosis definitions. Initial review found that most signals represented known adverse drug reactions or confounding. About 31% of signals met the highest signaling threshold. Conclusions: The GPS method was successfully applied to observational health plan data in a distributed data environment as a drug safety data mining method. There was substantial concordance between the GPS and TreeScan approaches. Key method implementation decisions relate to defining exposures and outcomes and informed choice of signaling thresholds.

Details

Language :
English
ISSN :
19994923
Volume :
5
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Pharmaceutics
Publication Type :
Academic Journal
Accession number :
edsdoj.8eb7d379bd084f9c9bcdc9bae0c49e43
Document Type :
article
Full Text :
https://doi.org/10.3390/pharmaceutics5010179