Table 1. Baseline characteristics of the patients.
Group A | Group B | |
(n = 242) | (n = 45) | |
Male, no. (%) | 183 (75.6) | 34 (75.6) |
Age, years, M (range) | 44 (21–81) | 42 (25–67) |
Weight, kg, M (range) | 69 (45–139) | 67 (49–116) |
Risk factor for HIV, no. (%) | ||
Previous iv drug use | 80 (33.0) | 14 (31.1) |
Hetero/homosexual | 154 (63.6) | 29 (64.4) |
Other | 8 (3.3) | 2 (4.4) |
Methadone treatment, no. (%) | 30 (12.3) | 8 (17.7) |
Nadir CD4/µl, M (range) | 198 (4–762) | 218 (6–480) |
Clinical category C, no. (%) | 57 (23.5) | 9 (20.0) |
Chronic hepatitis/cirrhosis, no. (%) | 69 (28.5)/21 (8.6) | 8 (17.7)/5 (11.1) |
HCV | 81 (90.0) | 9 (69.2) |
HBV | 5 (5.5) | 1 (7.6) |
HCV+HVB | − | 2 (14.3) |
Other | 3 (3.3) | 2 (14.3) |
No. previous ART, M (range) | 2 (1–9) | 2 (1–7) |
Months on previous ART, M (range) | 36 (1–186) | 37 (3–168) |
Previous antiretroviral regimen, no. (%) | ||
EFV +2 NRTIs | 134 (55.3) | 38 (84.4) |
NVP +2 NRTIs | 16 (6.6) | 7 (15.5) |
IP/rtv +2 NRTIs | 87 (35.9) | − |
3 NRTIs | 5 (2.0) | − |
Previous failure on NNRTIs, no. (%) | − | 45 (100) |
Available genotypic resistance test, no. (%) | 137 (56.6) | 45 (100) |
Wild type | 124 (90.5) | 17 (37.8) |
K103N | − | 22 (48.9) |
L100I or K101E or V179T | − | 3 (6.6) |
G190A | − | 2 (4.4) |
CD4/µl, M (range) | 473 (12–1360) | 468 (31–1351) |
HIV-RNA copies/ml, M (range) | <50 (<50–444867) | 982 (108–170000) |
HIV-RNA <50 copies/ml, no. (%) | 179 (74.0) | − |
Associated NRTIs, no. (%) | ||
TDF+FTC | 146 (60.3) | 22 (48.9) |
ABV +3TC | 83 (34.3) | 9 (20.0) |
AZT+TDF | 5 (2.1) | 10 (22.2) |
ABV+TDF | 5 (2.1) | 2 (4.4) |
AZT +3TC | 2 (0.8) | − |
ddI +3TC | 1 (0.4) | 2 (4.4) |
ETR 400 mg qd, no. (%) | 215 (88.8) | 29 (64.4) |
ART: antiretroviral treatment. NRTIs: nucleos(t)ide reverse-transcriptase inhibitors. NNRTIs: non-nucleoside reverse-transcriptase inhibitors. EFV: efavirenz. NVP: nevirapine. TDF: tenofovir. FTC: emtricitabine. ABV: abacavir. 3TC: lamivudine. AZT: zidovudine.