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Table 3 Pharmacokinetic parameters of isoniazid and rifampicin at standard and revised dosage

From: Pharmacokinetics of isoniazid, rifampicin, pyrazinamide and ethambutol in Indian children

Parameter

Isoniazid

Rifampicin

 

Standard dose, n = 64

Revised dose, n = 63

p value

Standard dose, n = 64

Revised dose, n = 63

p value

Dose, mg/kg, mean (SD)

5.6 (0.5)

11.4 (0.8)

<0.0001

11.2 (1.0)

15.2 (1.1)

<0.0001

2-hour concentration, μg/mL

0.4 (0.2, 0.8)

2.0 (1.2, 3.7)

<0.0001

8.8 (5.4, 11.9)

9.9 (5.4, 19.9)

0.06

C max , μg/mL

0.7 (0.3, 1.2)

3.4 (1.8, 5.0)

<0.0001

10.4 (7.2, 13.9)

12.0 (6.1, 24.3)

0.08

T max , hour

1 (1, 2)

1 (1, 2)

0.6

1.5 (1, 2)

2 (2, 3)

0.004

AUC 0–4 , μg/mL*hr

1.5 (0.8, 2.6)

7.0 (4.4, 11.9)

<0.0001

28.0 (19.3, 35.5)

30.5 (17.1, 58.9)

0.2

Low 2-hr concentration*, n (%)

59 (95.2)

43 (68.3)

<0.001

27 (43.5)

26 (41.3)

0.79

  1. Values are expressed as median (IQR) unless specified.
  2. *Low 2-hr concentrations: plasma concentration of isoniazid <3 μg/mL, rifampicin <8 μg/mL at 2 hour post drug time point.
  3. Cmax: maximum concentration, Tmax: Time needed to reach the maximum concentration, AUC: area under curve.