Document 1127 DOCN M94A1127 TI The efficacy of zidovudine in AIDS patients in Brazil. DT 9412 AU Sprinz E; Kronfeld M; Sfair A; Hospital de Clinicas Porto Alegre (HCPA), Brazil. SO Int Conf AIDS. 1994 Aug 7-12;10(2):202 (abstract no. PB0820). Unique Identifier : AIDSLINE ICA10/94371448 AB OBJECTIVE: Study the efficacy and safety of low doses of zidovudine (ZDV) in recently diagnosed AIDS patients in Brazil. PATIENTS & METHODS: Since July 1989 HIV patients willing to take part on research trials are being enrolled at HCPA, a national AIDS Reference Center in the south of Brazil. We analyze 128 patients from initial AIDS diagnosis (according to the CDC revisited criteria) to death, who have taken or not ZDV, 300 to 600 mg daily. Pregnancy, life expectancy less than 4 months or inability to follow orders were the exclusion criteria. ZDV group (677 patients willing to take the drug) is compared to the non-drug group (655 patients not willing to take ZDV). The groups were comparable in age, sex and AIDS index diagnosis. RESULTS: Four patients in ZDV and 5 in non-drug group were lost to follow-up. ZDV was well tolerated, but 8 patients (12%) had to discontinue the drug (independent of ZDV dose): 6 with severe bone marrow toxicity and 2 due to gastrointestinal intolerance. The mean survival time was 20 months in ZDV group (dose independent) and 12.5 months in non-ZDV group (p < 0.001). CONCLUSIONS: This is the first brazilian study on low doses of ZDV. ZDV was relatively safe and well-tolerated and increased the survival time of patients with AIDS. We strength the need of controlled studies using these doses of ZDV either alone or in association with other antiviral drugs. DE Acquired Immunodeficiency Syndrome/*DRUG THERAPY Human Support, Non-U.S. Gov't Zidovudine/ADMINISTRATION & DOSAGE/ADVERSE EFFECTS/*THERAPEUTIC USE CLINICAL TRIAL MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).