Stavudine and the peripheral nerve in HIV-1 infected patients

被引:0
|
作者
Hans-Jürgen von Giesen
Harald Hefter
Helmut Jablonowski
Gabriele Arendt
机构
[1] Department of Neurology,
[2] Heinrich Heine University,undefined
[3] Postfach 101007,undefined
[4] D-40001 Düsseldorf,undefined
[5] Germany e-mail: giesenhj@uni-duesseldorf.de Tel.: +49-211-8118971 Fax: +49-211-8118469,undefined
[6] Department of Medicine,undefined
[7] Heinrich Heine University,undefined
[8] Postfach 101007,undefined
[9] D-40001 Düsseldorf,undefined
[10] Germany,undefined
来源
Journal of Neurology | 1999年 / 246卷
关键词
Key words Human; immunodeficiency virus type 1; Stavudine; Polyneuropathy; Nerve conduction studies; Quantitative sensory testing;
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摘要
Stavudine (2′,3′-didehydro-3′deoxythymidine) is a pyrimidine analogue that may be of great value in combination antiretroviral therapy (ART) for treating patients infected with human immunodeficiency virus type 1 (HIV-1). We assessed potential neurotoxic side effects by comparing peripheral nerve function in patients receiving ART including stavudine (n = 107) with that of patients receiving ART with zidovudine (n = 103). A cross-sectional analysis of electroneurographic data revealed no significant differences. In a follow-up examination of 31 patients newly started on ART with stavudine we observed no significant effects of the drug on electrophysiological measures. At a daily dose of 1.0 mg/kg the incidence of peripheral nervous system disease in our patients was about 10%. Repeated follow-up analysis of 13 patients on stavudine showed a significant reduction in sural nerve amplitude. Quantitative sensory testing in 13 patients revealed no systematic effect of stavudine on small nerve fibers. Peripheral nerve function in HIV-1 seropositive patients on ART with stavudine did not differ significantly from that in patients on ART with zidovudine. Therefore stavudine at a daily dose of 1.0 mg/kg is an alternative for patients who do not tolerate, or who have become resistant to zidovudine and can be recommended as a first-line drug in combination ART.
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页码:211 / 217
页数:6
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