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Preliminary report of a toxicity study of hydroxyurea in sickle cell disease. French Study Group on Sickle Cell Disease.

机译:镰状细胞病中羟基脲毒性研究的初步报告。法国镰状细胞病研究小组。

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AIM: To evaluate the tolerance of hydroxyurea in children affected with sickle cell disease. DESIGN: Questionnaire study of French physicians likely to treat patients with sickle cell disease. Data were collected on 101 children with sickle cell disease, treated for a median of 22 months, 36 of whom were treated for more than three years. 13 children were younger than 5 years of age at inclusion. RESULTS: Hydroxyurea was stopped for medical reasons in 11 patients: 6 failures, 1 pregnancy, 1 cutaneous rash, 1 leg ulcer, 1 lupus. Acute lymphoblastic leukaemia occurred in a girl treated for 1.5 months with hydroxyurea, this short interval arguing against a causative association. One 17 year old boy had paraparesis after 8 years of treatment. CONCLUSIONS: No major short or medium term toxicity was related to hydroxyurea in this cohort of 101 children. However, the number of children treated for more than 3 years is too few to make firm conclusions on the long term tolerance of this drug.
机译:目的:评估镰状细胞病患儿对羟基脲的耐受性。设计:对可能治疗镰状细胞病患者的法国医师进行的问卷调查。收集了101名镰状细胞病儿童的数据,他们接受了平均22个月的治疗,其中36名儿童接受了三年以上的治疗。纳入时有13岁以下的5岁以下的儿童。结果:11例患者因医疗原因停用羟基脲:6例失败,1例妊娠,1例皮疹,1例腿溃疡,1例狼疮。一名接受羟基脲治疗1.5个月的女孩发生了急性淋巴细胞白血病,这种短暂的间隔认为是因果关系。治疗8年后,一名17岁男孩出现截瘫。结论:这组101名儿童的羟基脲没有重大的短期或中期毒性。但是,接受3年以上治疗的儿童人数太少,无法就这种药物的长期耐受性做出确切的结论。

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