Exact(4)
Outcomes for patients who had delirium at day one of the study will be calculated separately.
Third, the proportion of invited patients that participate in the study will be calculated.
Scores on the included outcomes measures and parameters in the study will be calculated according to published scoring algorithms.
The percentages of diagnosed diabetes at 12 and 24 months after the inclusion in the study will be calculated and the level of association with exposure to the educational intervention, considering the potential confounders, will be assessed.
Similar(56)
Kappa statistic and intra-class correlation coefficient among dental examiners for the studies will be calculated.
Homeostatic model assessment (HOMA) [ 57], a measure of insulin resistance and the primary measure of glycemic function in this study, will be calculated based on an established formula, each time fasting glucose and insulin are measured.
The aetiological fraction for matched case control studies will be calculated to estimate the fraction of cases with digestive disorders due to a specific pathogen.
The inter-rater reliability for inclusion of economic studies will be calculated and reported using κ statistics.
Primary endpoint of the study will be OS, calculated from the date of randomization to the date of death of the patient, from any cause.
For patients who receive fewer than the intended number of cycles of chemotherapy, the study duration will be calculated by the basis of the projected interval.
The number of patients diagnosed with delirium at least once in the seven days following initiation of the study intervention will be calculated for both the haloperidol and placebo group, and subsequently this number is divided by the total amount of patients assigned to the matching group, reflecting in-hospital delirium incidence ratio within seven days of initiation of the study intervention.
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