Table 2.
Random effects | ||||
Groups name | Variance | Standard deviation | ||
Clinical site (intercept) | 0.1371 | 0.3703 | ||
Number of observations, 2880; groups: site, 25 | ||||
Fixed effects | ||||
Estimate | Standard error | Z value | Pr (>|z|) | |
(Intercept) | − 2.734 | 0.16884 | − 16.192 | < 2e–16*** |
Pre-test probability | 3.04813 | 0.19998 | 15.243 | < 2e–16*** |
Method (original D+F or updated D+F 2011) | 0.43833* | 0.09312 | 4.707 | 2.51e–06*** |
Correlation of fixed effects | ||||
(Intercept) | Pre-test probability | |||
Pre-test probability | − 0.818 | |||
Method (original D+F or updated D+F 2011) | − 0.566 | 0.392 |
We performed a logistic regression analysis with the outcome (prevalence; CAD or no CAD) as dependent and the respective pre-test probability and the method of computation as predictors using the stacked data set (method original D+F versus updated D+F 2011). In order to take care of the variability between sites, we applied a random intercept for site. There is a significant effect of the method with a coefficient equal to 0.44, corresponding to an odds ratio of 1.55 (95% CI 1.29, 1.86). Significance codes: 0 = ‘***’, 0.001 = ‘**’, 0.01 = ‘*’, 0.05 = ‘.’ 0.1 = ‘ ’ 1; *Statistical significance