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氟喹诺酮类药物引起的免疫性血小板减少症:报告和综述。

Fluoroquinolone-induced immune thrombocytopenia: a report and review.

机构信息

Department of Haematology, Fremantle Hospital, Fremantle, Western Australia, Australia.

出版信息

Intern Med J. 2009 Sep;39(9):619-23. doi: 10.1111/j.1445-5994.2009.01996.x.

Abstract

Fluoroquinolones are an emerging but underrecognized cause of drug-induced thrombocytopenia. Due to their broad spectrum they are often used in empirical treatment of febrile neutropenic, thrombocytopenic patients following myelosuppressive chemotherapy. They are associated with a range of immunohaematopathology. A 76-year-old male developed severe thrombocytopenia following treatment with ciprofloxacin on two occasions for community-acquired pneumonia. The temporal association, response to dechallenge, dramatic response to rechallenge and exclusion of other causes combined with detection of platelet-reactive antibodies of the immunoglobulin G class against glycoprotein IIb/IIIa following ciprofloxacin rechallenge makes causality probable. We present a brief review of immunohaematopathology associated with fluoroquinolones and draw attention to the structural similarity between quinolones and quinine to explore potential mechanisms for the phenomenon. Fluoroquinolones can induce drug-dependent, platelet-reactive antibodies causing complement-mediated destruction of platelets. The underlying mechanism to explain this is unclear; however, we hypothesize that the chemical similarities shared with quinine may be contributory. When using these agents clinicians should be aware of the possibility of drug-induced thrombocytopenia or thrombotic thrombocytopenic purpura.

摘要

氟喹诺酮类药物是一种新兴但认识不足的药物诱导性血小板减少症的病因。由于其广谱性,它们常被用于经验性治疗发热性中性粒细胞减少、骨髓抑制化疗后血小板减少的患者。它们与一系列免疫血液病理学有关。一名 76 岁男性因社区获得性肺炎两次接受环丙沙星治疗后出现严重血小板减少。时间相关性、停药后反应、再用药后反应明显、排除其他原因以及在环丙沙星再用药后检测到针对糖蛋白 IIb/IIIa 的免疫球蛋白 G 类血小板反应性抗体,这些都提示可能存在因果关系。我们简要回顾了与氟喹诺酮类药物相关的免疫血液病理学,并注意到喹诺酮类药物和奎宁之间的结构相似性,以探讨这种现象的潜在机制。氟喹诺酮类药物可诱导药物依赖性、血小板反应性抗体,导致补体介导的血小板破坏。解释这种现象的潜在机制尚不清楚;然而,我们假设与奎宁共享的化学相似性可能是促成因素。当使用这些药物时,临床医生应意识到药物诱导性血小板减少症或血栓性血小板减少性紫癜的可能性。

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