Discontinuation | Continuation | p-value | |
---|---|---|---|
Participants (n, %) | 34 | 115 | |
Age, years [median; IQR] | 45 [39–56] | 37 [33–44] | 0.004 |
Males (n, %) | 34 (100%) | 114 (99%) | 0.515 |
Body weight, kg [median; IQR] | 58 [53–70] | 62[54–69] | 0.279 |
Body mass Index [median; IQR] | 21.2 [19.4–23.3] | 21.3[19.4–23.7] | 0.896 |
Body surface area, m2 [median; IQR] | 1.67 [1.56–1.78] | 1.72 [1.61–1.82] | 0.104 |
CD4 cell count, cells/μL [median; IQR] | 268 [143–398] | 272 [151–370] | 0.599 |
Estimated glomerular filtration rate, mL/min/1.73m2 [median; IQR] | 90[78–108] | 100[87–114] | 0.058 |
Participants with HIV-1-RNA level < 50 at time of sampling (n, %) | 15(44%) | 39(34%) | 0.233 |
Hypertension | 2(6%) | 2(2%) | 0.224 |
Diabetes mellitus | 2(6%) | 1(1%) | 0.129 |
Dyslipidemia | 1(3%) | 1(1%) | 0.406 |
Hyperuricemia | 2(6%) | 2(2%) | 0.224 |
AIDS (n, %) | 9(26%) | 38(33%) | 0.277 |
Use of Trimethoprim/sulfamethoxazole (n, %) | 6(18%) | 19(17%) | 0.877 |
Duration until measurement of plasma concentration (Median, days) | 28 | 28 | 0.614 |
HBV infection (n, %) | 1(3%) | 21(18%) | 0.018 |
HCV infection (n, %) | 1(3%) | 6(5%) | 0.497 |
Treatment naïve (n, %) | 33(97%) | 108(94%) | 0.475 |
Use of antiretroviral agents (n, %) | |||
Atazanavir/ritonavir (n, %) | 14(41%) | 41(36%) | 0.558 |
Lopinavir/ritonavir (n, %) | 7(21%) | 26(23%) | 0.803 |
Darunavir/ritonavir (n, %) | 8(23%) | 19(17%) | 0.351 |
Fosamprenavir/ritonavir( n, %) | 2(6%) | 15(13%) | 0.203 |
Efavirenz (n, %) | 0(0%) | 3(2%) | 0.457 |
Raltegravir (n, %) | 3(9%) | 11(9%) | 0.599 |