Table 2.
Characteristic1 | |
---|---|
Log10 viral load (copies/mL): | |
Mean (SD) | 3.1 (1.3) |
Median | 2.6 |
Viral load: n (%) | |
Undetectable (<400 copies/mL) | 130 (34.2) |
Detectable (≥ 400 copies/mL) | 250 (65.8) |
Missing | 5 |
CD4 count percent: n (%) | |
<15% | 19 (5.0) |
15 to 25% | 89 (23.4) |
>25% | 272 (71.6) |
Missing | 5 |
CD4 count (cells/mm3): n (%) | |
<200 | 5 (1.3) |
200–499 | 40 (10.4) |
≥500 | 340 (88.3) |
CDC Classification: n (%) | |
N | 28 (7.3) |
A | 105 (27.3) |
B | 116 (30.2) |
C | 135 (35.2) |
Missing | 1 |
WHO immunological staging: n (%) | |
None or not significant | 233 (61.3) |
Mild | 43 (11.3) |
Advanced | 33 (8.7) |
Severe | 71 (18.7) |
Missing | 5 |
Any ART prior to eligibility: n (%) | |
Yes | 344 (89.4) |
No | 41 (10.6) |
Duration of exposure to ART prior to eligibility (years): | |
Mean (SD) | 4.6 (2.8) |
Median | 4.5 |
Current ART regimen type: n (%) | |
No ART | 68 (17.7) |
PI-containing regimen | 214 (55.6) |
Non-PI-containing regimen | 103 (26.8) |
Self-reported ART adherence among those receiving ART2
: n (%) |
|
100% adherence | 279 (89.4) |
<100% adherence | 33 (10.6) |
Missing | 73 |
Where not available at time of eligibility, the most recent result prior to eligibility was selected. Missing data were not included in percentage calculations.
Percent adherence was determined in terms of numbers of ART doses missed relative to doses expected to be taken during the 3 day period prior to the study visit.