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

Table 3.

Unadjusted and adjusted predictors of virologic suppression and virologic failure among patients initiated on a nevirapine- or efavirenz-based regimen between April 2004 and August 2011 in Johannesburg, South Africa

Suppression within 12 months (n=9960) Failure within 12 months (n=8854)


Characteristic Suppression/N (%) Unadjusted RR (95% CI) Adjusted RR (95% CI) Failures/N(%) Unadjusted RR (95% CI) Adjusted RR (95% CI)
Regimen
Nevirapinea 641/712 (90.0%) 0.97 (0.95, 1.00) 0.98 (0.95, 1.00) 43/643 (6.7%) 1.79 (1.31, 2.44) 1.58 (1.13, 2.22)
Efavirenzb 8571/9248 (92.7%) Reference Reference 307/8211 (3.7%) Reference Reference
Year of ART initiation
2004/2005 1981/2179 (90.9%) Reference Reference 72/1944 (3.7%) Reference Reference
2006/2007 2600/2718 (95.7%) 1.05 (1.04, 1.07) 1.05 (1.03, 1.06) 93/2405 (3.9%) 1.04 (0.77, 1.41) 1.06 (0.78, 1.45)
2008/2009 2756/2870 (96.0%) 1.06 (1.04, 1.07) 1.05 (1.03, 1.06) 42/2404 (1.8%) 0.47 (0.32, 0.69) 0.51 (0.35, 0.76)
2010/2011 1875/2193 (85.5%) 0.94 (0.92, 0.96) 0.94 (0.90, 0.98) 143/2101 (6.8%) 1.84 (1.39, 2.42) 1.96 (1.17, 3.28)
Sex
Male 3266/3601 (90.7%) 0.97 (0.96, 0.98) 1.03 (1.02, 1.05) 139/3186 (4.4%) 1.17 (0.95, 1.45) 1.23 (0.98, 1.54)
Female 5946/6359 (93.5%) Reference Reference 211/5668 (3.7%) Reference Reference
Age at initiation
<30 1616/1769 (91.4%) Reference Reference 80/1565 (5.1%) Reference Reference
30–34 2098/2281 (92.0%) 1.01 (0.99, 1.03) 1.01 (0.99, 1.03) 84/2045 (4.1%) 0.80 (0.60, 1.08) 0.84 (0.61, 1.14)
35–39 2061/2224 (92.7%) 1.01 (1.00, 1.03) 1.02 (1.00, 1.04) 74/1995 (3.7%) 0.73 (0.53, 0.99) 0.73 (0.53, 1.01)
40–44 1460/1589 (91.9%) 1.01 (0.99, 1.03) 1.01 (0.99, 1.03) 51/1390 (3.7%) 0.72 (0.51, 1.01) 0.69 (0.48, 0.99)
≥45 1977/2097 (94.3%) 1.03 (1.01, 1.05) 1.03 (1.01, 1.05) 61/1859 (3.3%) 0.64 (0.46, 0.89) 0.68 (0.48, 0.96)
Baseline CD4+ Count (cells/mm3)
<50 2545/2796 (91.0%) 0.97 (0.95, 0.99) 0.96 (0.95, 0.98) 140/2480 (5.7%) 2.57 (1.73, 3.81) 2.74 (1.80, 4.17)
50–99 1784/1953 (91.4%) 0.97 (0.95, 0.99) 0.97 (0.95, 0.99) 72/1725 (4.2%) 1.90 (1.24, 2.91) 1.96 (1.25, 3.06)
100–199 3486/3724 (93.6%) 1.00 (0.98, 1.01) 0.99 (0.97, 1.01) 109/3328 (3.3%) 1.49 (1.00, 2.24) 1.52 (1.00, 2.31)
≥200 1397/1487 (94.0%) Reference Reference 29/1321 (2.2%) Reference Reference
WHO Stage
Stage I 3726/4013 (92.9%) Reference Reference 127/3577 (3.6%) Reference
Stage II 1584/1697 (93.3%) 1.01 (0.99, 1.02) 1.01 (0.99, 1.03) 55/1503 (3.7%) 1.03 (0.76, 1.41)
Stage III 2702/2932 (92.2%) 0.99 (0.98, 1.01) 1.00 (0.98, 1.01) 118/2607 (4.5%) 1.27 (1.00, 1.63)
Stage IV 1200/1318 (91.1%) 0.98 (0.96, 1.00) 1.00 (0.98, 1.02) 50/1167 (4.3%) 1.21 (0.88, 1.66)
Anaemia
No anaemia 2452/2626 (93.4%) Reference Reference 74/2336 (3.2%) Reference Reference
Mild anaemia 2244/2421 (92.7%) 0.99 (0.98, 1.01) 1.00 (0.98, 1.01) 81/2136 (3.8%) 1.20 (0.88, 1.63) 1.10 (0.81, 1.50)
Moderate anaemia 3423/3717 (92.1%) 0.99 (0.97, 1.00) 0.99 (0.98, 1.01) 148/3310 (4.5%) 1.41 (1.07, 1.86) 1.24 (0.93, 1.65)
Severe anaemia 715/764 (93.6%) 1.00 (0.98, 1.02) 1.02 (1.00, 1.04) 26/675 (3.9%) 1.22 (0.78, 1.89) 1.03 (0.66, 1.62)
BMI
<18.5 1348/1480 (91.1%) 0.98 (0.97, 1.00) 0.99 (0.97, 1.01) 62/1287 (4.8%) 1.28 (0.96, 1.69)
18.5–24.9 4948/5349 (92.5%) Reference Reference 180/4774 (3.8%) Reference
25–29.9 1574/1678 (93.8%) 1.01 (1.00, 1.03) 1.01 (1.00, 1.03) 53/1515 (3.5%) 0.93 (0.69, 1.25)
≥30 730/763 (95.7%) 1.03 (1.02, 1.05) 1.02 (1.00, 1.04) 22/661 (3.3%) 0.88 (0.57, 1.36)
NRTI
Stavudine 7276/7737 (94.0%) Reference Reference 221/6746 (3.3%) Reference Reference
Zidovudine 219/237 (92.4%) 0.98 (0.95, 1.02) 0.98 (0.94, 1.02) 3/213 (1.4%) 0.43 (0.14, 1.33) 0.49 (0.16, 1.51)
Tenofovir 1717/1986 (86.5%) 0.92 (0.90, 0.94) 1.00 (0.96, 1.04) 126/1895 (6.7%) 2.03 (1.64, 2.51) 1.14 (0.70, 1.85)
a

Nevirapine regimen includes tenofovir–lamivudine–nevirapine, zidovudine–lamivudine–nevirapine, stavudine–lamivudine–nevirapine;

b

efavirenz regimen includes tenofovir–lamivudine-efavirenz, zidovudine–lamivudine–efavirenz, stavudine–lamivudine–efavirenz.