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. 2008 Jan;13(1):6–16. doi: 10.1111/j.1365-3156.2007.01973.x

Table 1.

Baseline characteristics

Abacavir Nevirapine
Total participants 300 (100%) 300 (100%)
Randomization in main DART trial
 Laboratory and clinical monitoring 150 (50%) 149 (50%)
 Clinical monitoring only 150 (50%) 151 (50%)
Centre
 Entebbe, Uganda 149 (50%) 151 (50%)
 JCRC, Uganda 151 (50%) 149 (50%)
Sex
 Male 83 (28%) 87 (29%)
 Female 217 (72%) 213 (71%)
Age (years)
 ≤30 43 (14%) 68 (23%)
 >30–35 69 (23%) 55 (18%)
 >35–40 75 (25%) 90 (30%)
 >40–45 64 (21%) 41 (14%)
 >45–50 31 (10%) 32 (11%)
 >50 18 (6%) 14 (5%)
 Median (IQR) 37.6 (31.9–42.3) 36.3 (30.7–41.4)
WHO disease stage
 2 83 (28%) 76 (25%)
 3 173 (58%) 157 (52%)
 4 44 (15%) 67 (22%)
CD4 (cells/mm3)
 0–49 76 (25%) 88 (29%)
 50–99 75 (25%) 62 (21%)
 100–149 75 (25%) 84 (28%)
 150–199 74 (25%) 66 (22%)
 Median (IQR) [range] 99 (49–149) [1–199] 100 (40–145) [1–199]
Body mass index (BMI): median (IQR) 20.9 (18.9–23.5) 21.3 (19.3–23.8)
Haemoglobin (g/dl): mean (SD) 11.5 (1.8) 11.6 (1.7)
Neutrophils (×109/l): mean (SD) 1.5 (0.7) 1.6 (0.9)
Glomerular filtration rate (ml/min/1.73 m2)*: mean (SD) 85 (27) 85 (20)
ALT (IU): mean (SD) 27 (19) 27 (16)
AST (IU): mean (SD) 37 (25) 37 (20)
Women prescribed ARVs to prevent MTCT before entering DART (% of women) 4 (2%) 11 (5%)
Cotrimoxazole prophylaxis 120 (40%) 125 (42%)

The median CD4 at baseline is 99 rather than 99.5 cells/mm3 (as designed), because one participant was randomized in the wrong CD4 stratum in error.

ARV, antiretroviral; WHO, world health organisation.

*

Calculated according to the Cockcroft–Gault formula and adjusted for body surface area.

Including prophylaxis prescribed on the day of randomization.