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final program.qxd - Parallels Plesk Panel

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PP 4.23<br />

The increased liver toxicity of nevirapine over efavirenz does not depend on the<br />

female gender, and an initially elevated CD4+ lymphocyte count, in a single-centre<br />

comparative study with efavirenz conducted on 720 overall patients<br />

Roberto Manfredi, Leonardo Calza<br />

Infectious Diseases, University of Bologna, Italy<br />

Introduction. Some observations prompted to our attention a potentially increased<br />

hepatotoxicy of nevirapine, with significant rise among women with a baseline CD4+<br />

lymphocyte count >250 cells/µL. Aim of our study is to conduct an analysis from our<br />

database of patients treated prospectically with either nevirapine or efavirenz, to better<br />

define this claimed association. Patients and Methods. Among over 1,000 patients treated<br />

with HAART for >12 months, the hepatotoxicity pattern of both NNRTI was assessed<br />

according to three different backgrounds: antiretroviral-naïve patients starting a<br />

NNRTI-based regimen; a large spectrum of patients experienced with two to ten<br />

therapeutic lines (while remaining NNRTI-naïve); and <strong>final</strong>ly subjects who added for the<br />

first time a NNRTI only on late rescue therapies containing four drugs or more (and always<br />

including protease inhibitors). Results. Three hundred and 34 patients treated with<br />

nevirapine were compared with 386 individuals taking efavirenz in our survey, by a 12-30<br />

months multivariate analysis of liver enzyme abnormalities, together with a varied<br />

spectrum of epidemiological, clinical, and laboratory parameters. Instead of normal<br />

laboratory levels, we referred to the values found at treatment start. The two study groups<br />

were comparable as to epidemiological-clinical features and HIV virology, while a lower<br />

CD4+ count was found in subjects starting efavirenz (p

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