Abstract

ObjectiveEpidemiological research plays an important role in public health, facilitated by the meta‐analytic aggregation of epidemiological trials into a single, more powerful estimate. This form of aggregation is complicated when estimating the prevalence of a superordinate category of disorders (e.g., “any anxiety disorder,” “any cardiac disorder”) because epidemiological studies rarely include all of the disorders selected to define the superordinate category. In this paper, we suggest that estimating the prevalence of a superordinate category based on studies with differing operationalization of that category (in the form of different disorders measured) is both common and ill‐advised. Our objective is to provide a better approach.MethodsWe propose a multivariate method using individual disorder prevalences to produce a fully Bayesian estimate of the probability of having one or more of those disorders. We validate this approach using a recent case study and parameter recovery simulations.ResultsOur approach produced less biased and more reliable estimates than other common approaches, which were at times highly biased.ConclusionAlthough our approach entails additional effort (e.g., contacting authors for individual participant data), the improved accuracy of the prevalence estimates obtained is significant and therefore recommended.

Highlights

  • Epidemiology contributes to public health by characterizing the distribution of disorders as a means of informing public policy and optimally allocating resources (Oleckno, 2008)

  • We focus on an example from mental health, but our methods apply to any superordinate category

  • We report all parameters in terms of their median value as well as their highest density interval (HDI; Kruschke, 2014)

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Summary

| INTRODUCTION

Epidemiology contributes to public health by characterizing the distribution of disorders as a means of informing public policy and optimally allocating resources (Oleckno, 2008). Superordinate categories play an important role by easing the interpretation and categorization of related symptoms and simplifying the identification of at‐risk populations without becoming lost in the minutiae of individual disorders. We avoid aggregating prevalence estimates that vary in their operationalization, and instead model the prevalence estimates pertaining to the individual disorders and their interrelations. These parameters can be used to FAWCETT ET AL. We describe and validate our model using a case study and parameter recovery simulations

| METHODS
| RESULTS
Method
| DISCUSSION
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