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药物性血小板减少症在体内和体外均与IgG与血小板的结合增加有关。

Drug-induced thrombocytopenia is associated with increased binding of IgG to platelets both in vivo and in vitro.

作者信息

Kelton J G, Meltzer D, Moore J, Giles A R, Wilson W E, Barr R, Hirsh J, Neame P B, Powers P J, Walker I, Bianchi F, Carter C J

出版信息

Blood. 1981 Sep;58(3):524-9.

PMID:6973346
Abstract

Thrombocytopenia is a common serious adverse effect of drug treatment. A variety of in vitro diagnostic techniques to confirm the diagnosis are available, but the majority lack sufficient sensitivity to detect all cases of drug-induced thrombocytopenia. We studied 19 patients with suspected drug-induced thrombocytopenia and demonstrated that platelet-associated IgG (PAIgG) was elevated in all at the time of thrombocytopenia, and PAIgG returned to normal levels as the thrombocytopenia resolved. In the majority of patients, the platelet count rapidly returned to normal after the drug was discontinued; however, in six patients, the thrombocytopenia persisted well beyond the period of time that the offending drug would be expected to be cleared from the blood. In 13 patients, serum obtained after recovery was used to identify the drug responsible for the thrombocytopenia in an in vitro assay. In all cases, the addition of the drug historically associated with the thrombocytopenic episode was associated with an increased binding of IgG to control platelets. For uncertain reasons, the concentration of drug required to increase the in vitro binding of IgG to test platelets was often more than the concentration usually achieved in vivo. Wider application of these techniques may provide better understanding of the clinical characteristics and mechanisms responsible for drug-induce thrombocytopenia.

摘要

血小板减少症是药物治疗常见的严重不良反应。现有多种体外诊断技术可用于确诊,但大多数技术缺乏足够的敏感性来检测所有药物性血小板减少症病例。我们研究了19例疑似药物性血小板减少症患者,结果表明,所有患者血小板减少时血小板相关IgG(PAIgG)均升高,随着血小板减少症的缓解,PAIgG恢复至正常水平。大多数患者停药后血小板计数迅速恢复正常;然而,有6例患者的血小板减少症持续时间远远超过预期致病药物从血液中清除的时间。在13例患者中,康复后采集的血清用于在体外试验中鉴定导致血小板减少症的药物。在所有病例中,加入既往与血小板减少发作相关的药物后,IgG与对照血小板的结合增加。出于不确定的原因,增加IgG与测试血小板体外结合所需的药物浓度通常高于体内通常达到的浓度。更广泛地应用这些技术可能有助于更好地了解药物性血小板减少症的临床特征和发病机制。

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