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A Bayesian hierarchical model for characterizing the diffusion of new antipsychotic drugs

Authors :
Julie M. Donohue
Chenyang Gu
Haiden A. Huskamp
Sharon-Lise T. Normand
Source :
Biometrics
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

New prescription medications are a primary driver of spending growth in the United States. For patients with severe mental illnesses, second generation antipsychotic (SGA) medications feature prominently. However, many SGAs are costly, particularly before generic entry, and some may increase the risk of diabetes. Because physicians play a prominent role in new prescription adoption, understanding their prescribing behaviors is policy-relevant. Several features of prescription data, such as different antipsychotic choice sets over time, variable physician prescription volumes, and correlation among drug choices within physicians, complicate inferences. We propose a multivariate Bayesian hierarchical model with piecewise random effects to characterize the diffusion of new antipsychotic drugs. This model captures the complex prescriber-specific relationships among the different diffusion processes and takes advantage of the Bayesian paradigm to quantify uncertainty for all parameters straightforwardly. To evaluate the prescribing patterns for each physician, we propose various indices to identify early new SGA adopters. A sample of nearly 17,000 U.S. physicians whose antipsychotic drug prescribing information was collected between January 1, 1997 and December 31, 2007 illustrates the methods. Determinants of high prescription rates and adoption speeds of new SGAs included physician sex, age, hospital affiliation, physician specialty, and office location. Large within- and between-provider variations in prescribing patterns of new SGAs were identified. Early adopters for one drug were not early adopters for another drug.

Details

ISSN :
15410420 and 0006341X
Volume :
77
Database :
OpenAIRE
Journal :
Biometrics
Accession number :
edsair.doi.dedup.....171fc089f5548d3d614d5a65f8f49838
Full Text :
https://doi.org/10.1111/biom.13324