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. 2014 Oct 22;17(1):19065. doi: 10.7448/IAS.17.1.19065

Table 1.

Patient characteristics at ART initiation and treatment outcomes for patients initiating a nevirapine- or efavirenz-based regimen between April 2004 and August 2011 in Johannesburg, South Africa

Variable Exposure Nevirapine Efavirenz
Total N 878 (100%) 11,962 (100%)
Year of ART initiationa 2004/2005 227 (25.9%) 2513 (21.0%)
2006/2007 266 (30.3%) 3247 (27.1%)
2008/2009 242 (27.6%) 3485 (29.1%)
2010/2011 143 (16.3%) 2717 (22.7%)
Sex Male 312 (35.5%) 4566 (38.2%)
Female 566 (64.5%) 7396 (61.8%)
Age (years) Median (IQR) 33.0 (28.4–39.1) 37.2 (31.9–43.9)
<30 283 (32.2%) 2033 (17.0%)
30–34 243 (27.7%) 2672 (22.3%)
35–39 169 (19.3%) 2644 (22.1%)
40–44 103 (11.7%) 1963 (16.4%)
≥45 80 (9.1%) 2650 (22.2%)
CD4 count (cells/mm3) Median (IQR) 100.5 (42–160) 98 (36–169)
<50 242 (27.6%) 3741 (31.3%)
50–99 192 (21.9%) 2305 (19.3%)
100–199 394 (44.9%) 4181 (35.0%)
≥200 50 (5.7%) 1735 (14.5%)
WHO Stage Stage I 419 (47.7%) 4519 (37.8%)
Stage II 127 (14.5%) 1932 (16.2%)
Stage III 247 (28.1%) 3585 (30.0%)
Stage IV 85 (9.7%) 1926 (16.1%)
BMI (kg/m2) Median (IQR) 22.0 (19.7–25.1) 21.7 (19.2–24.9)
Missing 75 (8.5%) 1169 (9.8%)
<18.5 114 (13.0%) 2034 (17.0%)
18.5–24.9 481 (54.8%) 6125 (51.2%)
25.0–29.9 136 (15.5%) 1823 (15.2%)
≥30 72 (8.2%) 811 (6.8%)
Haemoglobin (g/dL) Median (IQR) 11.3 (9.7–12.7) 11.0 (9.5–12.5)
Anaemia Missing 50 (5.7%) 569 (4.8%)
No anaemia 236 (26.9%) 2900 (24.2%)
Mild anaemia 212 (24.2%) 2720 (22.7%)
Moderate anaemia 317 (36.1%) 4627 (38.7%)
Severe anaemia 63 (7.2%) 1146 (9.6%)
NRTIb Stavudine 728 (82.9%) 9235 (77.2%)
Zidovudine 24 (2.7%) 293 (2.5%)
Tenofovir 126 (14.4%) 2434 (20.4%)
Outcome at 12 months Alive 700 (79.7%) 9158 (76.6%)
Dead 55 (6.3%) 1006 (8.4%)
Lost to follow-up 88 (10.0%) 1287 (10.8%)
Transferred out 35 (4.0%) 511 (4.3%)
Achieved viral suppressionc 641 (90.0%) 8571 (92.7%)
Experienced virologic failured 43 (6.1%) 307 (3.3%)
a

A year is defined as a cohort year, starting 1 April and ending 31 March of the following year. The 2011 cohort starts in April and ends in August of the same year;

b

nucleoside reverse transcriptase inhibitor (NRTI);

c

among patients with at least one viral load between one month and one year after ART initiation;

d

among patients with at least one viral load after four months of follow-up.