“…The remaining 5169 patients are all added to the validation cohort Sensitivity and specificity, discriminatory power and 95% confidence interval, number of tests avoided, negative predictive value, positive predictive value | Not mentioned | Isma'eel et al [ 42 ] | The derivation cohort was randomly chosen 30 out of the 59 patients who tested positive were added randomly to the derivation cohort, and 30 out of the remaining 427 patients who tested negative were also added randomly to the derivation cohort. The remaining 426 patients (29 positive, 397 negative) were all added to the testing cohort; during the training phase, the 60 patients that are used for training were split 80% for pure training and 20% for validation | Negative and positive predictive values, descriminatory power, percentage of avoided tests, sensitivity and specificity | Not mentioned |
Jovanovic et al [ 43 ] | The sample was randomly divided into 3 parts: training, testing, and validation sample | Area under the receiver operating curve, sensitivity, specificity, and positive and negative predictive values | Not mentioned |
Kang et al [ 27 ] | Four-fold cross validation, 75/25 split (training/validation) | Area under the receiver operating curve, accuracy, precision, recall | Not mentioned |
Karhade et al [ 28 ] | tenfold cross validation | Discrimination (c-statistic or area under the receiver operating curve), calibration (calibration slope, calibration intercept), and overall performance (Brier score) | Multiple imputation with the missForest methodology was undertaken for variables with less than 30% missing data |
Kebede et al [ 29 ] | 10% cross validation, 90/10 split (training/testing) | Area under the receiver operating curve; classification accuracy-true positive, false positive, precision, recall | If information is incomplete, un-readable or their manual record is lost, patients were excluded from the study |
Khanji et al [ 47 ] | Ten-fold cross validation | Akaike Information Criterion, area under the receiver operating curve | Excluded patients with missing data at the end of the study (± 6 months) |
Kim et al [ 30 ] | |
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