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Submission Type

Empirical Research

Keywords

data-mining, population health, data analysis method, research networks, pharmacovigilance, signal detection

Abstract

Objective: To perform sample size calculations when using tree-based scan statistics in longitudinal observational databases.

Methods: Tree-based scan statistics enable data-mining on epidemiologic datasets where thousands of disease outcomes are organized into hierarchical tree structures with automatic adjustment for multiple testing. We show how to evaluate the statistical power of the unconditional and conditional Poisson versions. The null hypothesis is that there is no increase in the risk for any of the outcomes. The alternative is that one or more outcomes have an excess risk. We varied the excess risk, total sample size, frequency of the underlying event rate, and the level of across-the-board healthcare utilization. We also quantified the reduction in statistical power resulting from specifying a risk window that was too long or too short.

Results: For 500,000 exposed people, we had at least 98% power to detect an excess risk of 1 event per 10,000 exposed for all outcomes. In the presence of potential temporal confounding due to across-the-board elevations of healthcare utilization in the risk window, the conditional tree-based scan statistic controlled type I error well, while the unconditional version did not.

Discussion: Data-mining analyses using tree-based scan statistics expand the pharmacovigilance toolbox, ensuring adequate monitoring of thousands of outcomes of interest while controlling for multiple hypothesis testing. These power evaluations enable investigators to design and optimize implementation of retrospective data-mining analyses.

Creative Commons License

Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License.

DOI

10.13063/2327-9214.1264

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