| Literature DB >> 33413716 |
Jordan Edwards1,2, A Demetri Pananos1, Amardeep Thind1,3,4, Saverio Stranges1,4,5, Maria Chiu6,7, Kelly K Anderson1,2,6,8.
Abstract
AIMS: There is currently no universally accepted measure for population-based surveillance of mood and anxiety disorders. As such, the use of multiple linked measures could provide a more accurate estimate of population prevalence. Our primary objective was to apply Bayesian methods to two commonly employed population measures of mood and anxiety disorders to make inferences regarding the population prevalence and measurement properties of a combined measure.Entities:
Keywords: Bayesian analysis; Common mental disorders; diagnosis and classification; epidemiology; prevalence; research design and methods
Mesh:
Year: 2021 PMID: 33413716 PMCID: PMC8057492 DOI: 10.1017/S2045796020001080
Source DB: PubMed Journal: Epidemiol Psychiatr Sci ISSN: 2045-7960 Impact factor: 6.892
Concordance between survey structured interview and administrative data diagnosed mood and anxiety disorders in Ontario, Canada (Edwards et al., 2019a)
| (+) Admin-derived diagnosed | (−) Admin-derived diagnosis | ||
|---|---|---|---|
| (+) Survey-derived diagnosis | 164 (3.9%) | 415 (9.9%) | 579 (13.9%) |
| (–) Survey-derived diagnosis | 268 (6.4%) | 3310 (79.6%) | 3578 (86.1%) |
| 432 (10.4%) | 3725 (89.6%) | 4157 (100.0%) |
Fig. 1.Marginal posterior density for the prevalence of mood or anxiety disorders in Ontario, Canada, using data from both survey and administrative data combined. Note: π represents posterior prevalence using both administrative and survey data, δ1 represents sensitivity for administrative data, and γ1 represents specificity for administrative data, δ2 represents sensitivity for survey data, and γ2 represents specificity for survey data.
Marginal prior and posterior medians and 95% CI of the posterior equally tailed 95% CI for the prevalence (π) and sensitivities (δ1, δ2) and specificities (γ1, γ2) for each measure of mood and anxiety disorder and the combination of the two measures
| Prior information | Admin-derived diagnosis | Survey-derived diagnosis | Both measures | |||||
|---|---|---|---|---|---|---|---|---|
| Mean | 95% CI | Mean | 95% CI | Mean | 95% CI | Mean | 95% CI | |
| 7.4 | 5.4–9.6 | 13.9 | 1.2–25.0 | 8.6 | 6.8–10.6 | |||
| Admin-derived | ||||||||
| 62.9 | 59.9–66.8 | 62.9 | 58.8–66.8 | 62.6 | 58.6–66.6 | |||
| 93.8 | 92.8–94.7 | 93.8 | 93.0–94.6 | 94.2 | 93.4–95.0 | |||
| Survey-derived | ||||||||
| 55.3 | 41.9–68.6 | 55.2 | 51.3–59.1 | 63.5 | 54.6–73.4 | |||
| 93.7 | 89.9–97.4 | 93.0 | 86.5–99.4 | 91.0 | 89.8–92.1 | |||
Note: π represents posterior prevalence, δ1 represents sensitivity for administrative data, and γ1 represents specificity for administrative data, δ2 represents sensitivity for survey data, and γ2 represents specificity for survey data.
Estimated from (se) (Higgins, 2008).
Fig. 2.Results from the sensitivity analysis testing the impact of variation in psychometric properties on the posterior prevalence. Note: π represents posterior prevalence using both administrative and survey data, δ1 represents sensitivity for administrative data, and γ1 represents specificity for administrative data, δ2 represents sensitivity for survey data, and γ2 represents specificity for survey data. We find that changes in the prior expectation for the sensitivities of both survey and administrative data, as well as the specificity of the administrative data, do not appreciably change the expected prevalence. We do find that changes to the specificity of the survey data have a considerable influence on the expected prevalence. The coloured intervals represent the credible intervals of the expected prevalence with three different values of the specificity for the survey data. Red represents a prior expectation for the specificity of 88%, green 93% and blue 98%.
Fig. 3.Posterior predictive checks to assess model reliability. Note: Our model estimates for the expected count in each cell are shown as a black dot. Associated 95% credible intervals are indicated. The vertical lines indicate the observed counts in each cell. We note that since our expectations are close to the observations, our model is capable of reproducing our data.