Stavudine (2',3'-didehydro-3'deoxythymidine) is a pyrimidine analogue that
may be of great value in combination antiretroviral therapy (ART) for treat
ing patients infected with human immunodeficiency virus type 1 (HIV-1). We
assessed potential neurotoxic side effects by comparing peripheral nerve fu
nction in patients receiving ART including stavudine (n = 107) with that of
patients receiving ART with zidovudine (n = 103). A cross-sectional analys
is of electroneurographic data revealed no significant differences. In a fo
llow-up examination of 31 patients newly started on ART with stavudine we o
bserved no significant effects of the drug on electrophysiological measures
. At a daily dose of 1.0 mg/kg the incidence of peripheral nervous system d
isease in our patients was about 10%. Repeated follow-up analysis of 13 pat
ients 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 sero
positive patients on ART with stavudine did not differ significantly from t
hat 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 ha
ve become resistant to zidovudine and can be recommended as a first-line dr
ug in combination ART.