Comparison of two dose regimens of zidovudine in an open, randomized, multicentre study for severe HIV‐related thrombocytopenia
作者:
Giuseppe Landonio,
Paola Cinque,
Annamaria Nosari,
Sergio Gafa,
Francesco Rizzo,
Massimo Coen,
Umberto Tirelli,
Liliana Caggese,
Umberto di Luzio Paparatti,
Adriano Lazzarin,
期刊:
AIDS
(OVID Available online 1993)
卷期:
Volume 7,
issue 2
页码: 209-212
ISSN:0269-9370
年代: 1993
出版商: OVID
关键词: HIV-related thrombocytopenia;zidovudine;dose;therapy
数据来源: OVID
摘要:
ObjectiveTo compare the effect of two dose regimens of zidovudine in the treatment of severe HIV-related thrombocytopenia (TP).Design: Eighty-four patients with severe HIV-related TP and platelet counts < 50 x 109/I were enrolled in an open study at six centres. Patients were randomized into two groups to receive zidovudine (group A, 500 mg per day; group B, 1000 mg per day) for 6 months.MethodsPlatelet counts were determined monthly and patients categorized as complete responders (CR; platelets > 100 x 109/I), partial responders (PR; platelets > 50 to < 100 x 109/I), or failures (F; platelets to < 50 x 109/I). CD4+ and CD8 + lymphocytes, HIV antigenaemia, β2-microglobulin, white blood cells, mean cell volume and haemoglobin were also determined.ResultsSeventy-one patients (35 and 36 in groups A and B, respectively) completed the study; 11.4% of group A patients were CR and 45.7% PR; 38.9% of group B were CR and 33.3% PR. Increase in mean platelet counts was dose-related, more rapid in the higher dose group and remained significantly higher after 6 months of treatment (56.4 x 109/I in group A versus 98.2 x 109/I in group B; P < 0.01).ConclusionsThe results confirm the efficacy of zidovudine in the treatment of severe HIV-related TP. The average for CR and PR in the two groups was 64.8%; the higher dose of zidovudine was more effective at increasing platelet counts.
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