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Oral iron chelation with deferiprone.

机译:与去铁酮口服铁螯合。

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摘要

Deferiprone is the most widely studied oral iron chelator and, at present, the only one shown to be effective in achieving negative iron balance in long-term clinical trials for chronic iron overload. Because of its adverse effects (e.g., agranulocytosis and arthropathy) its use is presently restricted to clinical trials and to countries where desferrioxamine is unavailable. Deferiprone was licensed for clinical use in India in 1995. Clinical trials are in progress in many centers worldwide that will provide further information on the long-term effectiveness of deferiprone as well as on the incidence of serious adverse effects in patients with iron overload. Trials of combined use of deferiprone and desferrioxamine are also in progress. In the meantime, deferiprone is an acceptable alternative for patients who cannot use desferrioxamine because of serious adverse effects, lack of compliance, or unavailability. Elucidation of the mechanisms involved in the agranulocytosis and arthropathy associated withdeferiprone is still needed, as are methods to predict individual susceptibility to these adverse effects and ways of preventing them. In addition, new indications for iron-chelating therapy are continuously being explored.
机译:Deferiprone是研究最广泛的口服铁螯合剂,目前,在慢性铁超负荷的长期临床试验中,唯一显示出可以有效实现铁负平衡的药物。由于其不利影响(例如粒细胞缺乏症和关节病),其使用目前仅限于临床试验和不能使用去铁胺的国家。 Deferiprone于1995年在印度获得临床使用许可。全球许多中心正在进行临床试验,这些试验将提供有关Deferiprone的长期有效性以及铁超负荷患者严重不良反应发生率的进一步信息。联合使用去铁酮和去铁胺的试验也在进行中。同时,对于由于严重的不良反应,依从性不足或无法使用而不能使用去铁敏的患者,去铁酮是可以接受的替代药物。仍然需要阐明与去铁酮相关的粒细胞缺乏症和关节炎所涉及的机制,以及预测个体对这些不良反应的敏感性的方法以及预防方法。此外,正在不断探索铁螯合疗法的新适应症。

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