Table 1.
Characteristic | Value |
---|---|
Evaluable children, n(%) | 18 (100) |
Median age, months (IQR) | 23.4 (12.1–27.8) |
Age range | |
3–<12 months, n (%) | 4 (22) |
12–<24 months, n (%) | 6(33) |
24–<36 months, n (%) | 8 (44) |
Gender | |
Male, n (%) | 10(56) |
Female, n (%) | 8 (44) |
Median body weight, kg (IQR) | 11.3 (10.3–13.0) |
Ethnic origin | |
White, n (%) | 3 (17) |
Black, n (%) | 14(78) |
Mixed, n (%) | 1 (6) |
CDC stage | |
N, n (%) | 7 (39) |
A, n (%) | 3(17) |
B, n (%) | 1 (6) |
C, n (%) | 7 (39) |
Median cumulative ART exposure, months (IQR) | 11.3 (7.4–21.6) |
Antiretroviral therapy combinationa | |
3TC+ABC+NVP (±AZT or ±d4T), n (%) | 10 (56) |
3TC+ABC+LPV/r (±AZT), n (%) | 7 (39) |
FTC+ABC+LPV/r, n (%) | 1 (6) |
All children were taking all antiretroviral therapy (ART) drugs twice daily, with two exceptions: one child, who was on lamivudine (3TC) and abacavir (ABC), was taking nevirapine (NVP) once daily; and one child on abacavir (ABC) and lopinavir/ritonavir (LPV/r) was taking emtricitabine (FTC) once daily. The child evaluated for ABC only was 24–<36 months of age, female, 15.0 kg, White, CDC stage C and taking FTC, ABC plus LPV/r. AZT, zidovudine; d4T, stavudine; IQR, interquartile range.