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. 2018 Apr 20;58(1):53–61. doi: 10.1007/s40262-018-0658-1

Table 1.

Demographics of all patients, and those included in the pharmacokinetic analysis after removing data with missing dose history or sample timing information

Variable All patients (n = 128) PK patients (n = 117)
No. of TDM samples 580 338
No. of samples/patients, median (range) 5 (1–14) 3 (1–11)
Speciality, BMT/Haem/Imm/othera 94/7/19/8 87/6/17/7
Age, years (range) 5.9 (0.5–18.9) 5.7 (0.5–18.5)
Weight, kg (range) 17.92 (6.05–71) 17.8 (6.05–74.8)
Sex, male/female 47/81 43/74
Dose, mg (range) 200 (32–700) 200 (32–630)
Dose, mg/kg (range) 12.99 (2.58–48.95) 13.11 (2.67–48.95)
Dose, mg/m2, (range) 326 (84–921) 326 (84–921)
Concentration, mg/L (range) 0.96 (0.07–4.99) 0.8 (0.07–4.99)
Sample time after dose, h(range) 6.96 (0.02–24.78) 6.52 (0.02–24.78)
Dose frequency, doses/day (range) 3 (1–4) 3 (1–4)
% samples when patient had diarrhoea 18 20
% samples when patient also taking PPI 61 68
% samples when patient also taking H2 receptor antagonist 28 32

BMT bone marrow transplant, Haem haematology, Imm immumology, H2 histamine H2-receptor antagonist, PK pharmacokinetic, PPI proton pump inhibitor, TDM therapeutic drug monitoring

a‘Other’ includes patients undergoing solid organ transplantation, those from gastroenterology, and surgical patients