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Additionally, among the original 260 T2DM participants recruited for the study, 19 were excluded, mainly because of missing clinical data.
One article had to be excluded or pooled with another because of possible double publication of the same cohort (Grecchi (b) [15]), one article because of missing follow-up times (Hvaring [16]), one because of missing clinical data (Kjaer [17]), and two articles because of missing numerical data (Dellavia [18, 19]).
†Two TB patients excluded because of missing clinical data, 4 from multivariate analysis (n = 78).
Among them, 68 patients were excluded because of missing clinical information and/or biochemical indices.
Sixteen patients were excluded because of missing clinical data or serum samples; 263 were included in the study.
Of these 212 cases, eight were excluded due to lack/poor quality DNA and another three because of missing clinical data.
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When investigators cannot impute missing clinical values (because they are not missing at random), one of the less biased methods is to analyze the subgroup of patients with complete data for all characteristics, the method we adopted[ 13].
Thirdly, a significant proportion of residents were excluded because of missing or inadequate clinical and biomarker data.
Third, a significant proportion of residents were excluded because of missing or inadequate clinical and biomarker data.
Five of these (20%) met our criteria for clinical benefit following treatment with capecitabine, and in one case clinical benefit could not be evaluated because of missing data.
Of these, 509 were excluded because of missing information on death, leaving 6891 patients from 12 clinical centres throughout Germany for analysis (see supplementary figure 1).
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