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15th International AIDS ConferenceBangkok, Thailand - July 11-16, 2004 |
Int Conf AIDS 2004 Jul 11-16; 15:(abstract no. B10238)
Sherer R, Adeyemi OM, Simeone E, Despotes J, Tschampa J
CORE Center, Cook County Hospital, Chicago, United States
BACKGROUND: To describe the efficacy, durability and tolerability of Lopinavir/r (LPV/r) based HAART regimens in an urban clinic population.
METHODS: A retrospective-prospective observational study. Between Oct 2002 and Oct 2003, HIV+ patients currently receiving LPV/r were enrolled in this study. Baseline information collected included demographics, Hepatitis B/C sero-status, antiretroviral history, baseline and nadir CD4. At each study visit, data on LFTs, CD4, VL, lipids, ARV changes were collected, and waist/hip measurements were performed. Initial data on the first 12 weeks of study follow up are presented.
RESULTS: 120 HIV+ pts who had received LPV/r for a median duration of 6 months (0-41 months) were enrolled. The mean age was 44 years, 77% were male, 74% AA, 17% Caucasian and 8% Hispanic. At baseline (initiation of LPV/r) 18 pts (15%) were ARV naïve, 66 pts (55%) had prior NNRTI experience; 79 pts (66%) had prior PI; 51pts (43%) had prior 3 class experience. In addition to LPV/r, 105 pts (91%) received NRTI's, 37pts (32%) NNRTI's and 15 (13%) a 2nd PI. At baseline the median CD4 and HIV RNA of the cohort were 177/mm3 and 4.34 log10copies/ml. CD4 and HIV RNA changes shown in the table (all values median).
CONCLUSIONS: In this diverse study population in a "real world" setting, there was a sustained immunologic and virologic response to LPV/r based regimens with the greatest benefits in treatment naïve patients. [table: see text]
040711
B10238
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