In toxicology, the validation of the concurrent control by historical control data (HCD) has become requirements. This validation is usually done by historical control limits (HCL) which in practice are often graphically displayed in a Sheward control chart like manner. In many applications, HCL are applied to dichotomous data, e.g. the number of rats with a tumor vs. the number of rats without a tumor (carcinogenicity studies) or the number of cells with a micronucleus out of a total number of cells. Dichotomous HCD may be overdispersed and can be heavily right- (or left-) skewed, which is usually not taken into account in the practical applications of HCL. To overcome this problem, four different prediction intervals (two frequentist, two Bayesian), that can be applied to such data, are proposed. Comprehensive Monte-Carlo simulations assessing the coverage probabilities of seven different methods for HCL calculation reveal, that frequentist bootstrap calibrated prediction intervals control the type-1-error best. Heuristics traditionally used in control charts (e.g. the limits in Sheward np-charts or the mean plus minus 2 SD) as well a the historical range fail to control a pre-specified coverage probability. The application of HCL is demonstrated based on a real life data set containing historical controls from long-term carcinogenicity studies run on behalf of the U.S. National Toxicology Program. The proposed frequentist prediction intervals are publicly available from the R package predint, whereas R code for the computation of the Bayesian prediction intervals is provided via GitHub.
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