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Journal ArticleDOI

Trend towards decreased survival in patients infected with HIV resistant to zidovudine.

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TLDR
The survival of 35 patients with AIDS or advanced HIV infection on treatment with zidovudine was related to the viral sensitivity to the drug and to the CD4+ cell count and large studies of combination or alternation therapy with several anti-HIV drugs should be given high priority.
Abstract
The survival of 35 patients with AIDS or advanced HIV infection on treatment with zidovu-dine was related to the viral sensitivity to the drug and to the CD4+ cell count. 14 patients died, the survivors were followed up for an average of 804 days. In a univariate Cox model, survival was strongly related to Iog IC90 (p = 0.0003) and to the CD4+ count (p = 0.0002). In a bivariate model, Iog IC90 and the CD4+ count contributed to the prediction of survival (p = 0.12 and 0.06, respectively). Large studies of combination or alternation therapy with several anti-HIV drugs should be given high priority.

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Lack of synergy in the inhibition of HIV-1 reverse transcriptase by combinations of the 5'-triphosphates of various anti-HIV nucleoside analogs.

TL;DR: Results indicated that synergistic inhibition of the HIV-1 reverse transcriptase is not responsible for the synergistic antiviral activity seen in cell culture with combinations of these nucleoside analogs.
Journal Article

A randomized controlled trial of a reduced daily dose of zidovudine in patients with the acquired immunodeficiency syndrome

TL;DR: In this article, a randomized controlled trial was conducted to evaluate the efficacy and safety of a reduced dose of zidovudine for patients with advanced disease caused by the human immunodeficiency virus type 1 (HIV).
Journal ArticleDOI

Zidovudine in HIV infection.

Antagonistic evolutionary pathways of hiv-1 resistance to nucleoside reverse transcriptase inhibitors: a virological, biochemical and clinical investigation

TL;DR: It is proposed that K65R and TAMs represent two different pathways of NRTI resistance that exhibit bi-directional phenotypic antagonism and counterselection in vivo and will help to optimize current and future therapy for HIV-1 infection.
References
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Journal ArticleDOI

The efficacy of azidothymidine (AZT) in the treatment of patients with AIDS and AIDS-related complex: a double-blind placebo-controlled trial.

TL;DR: It is demonstrated that AZT administration can decrease mortality and the frequency of opportunistic infections in a selected group of subjects with AIDS or AIDS-related complex, at least over the 8 to 24 weeks of observation in this study.
Journal ArticleDOI

HIV with reduced sensitivity to zidovudine (AZT) isolated during prolonged therapy

TL;DR: It would be premature to alter any treatment protocols for HIV-infected individuals at present, as it cannot be determined from this small sample of patients whether development of a less sensitive virus phenotype results in clinical resistance.
Journal ArticleDOI

A double‐blind, placebo‐controlled trial

TL;DR: Results confirm previous findings that suppression of rheumatoid synovitis may be induced by SSZ, within 2 months after full maintenance doses are reached.
Journal ArticleDOI

A Randomized Controlled Trial of a Reduced Daily Dose of Zidovudine in Patients with the Acquired Immunodeficiency Syndrome

TL;DR: A randomized controlled trial in 524 subjects who had had a first episode of Pneumocystis carinii pneumonia found that the efficacy and safety of a reduced dose of zidovudine were superior to the standard-treatment group and the low-dose group.
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