Suppr超能文献

万古霉素诱导的血小板减少症,未分离出药物依赖抗体。

Vancomycin-induced thrombocytopenia without isolation of a drug-dependent antibody.

机构信息

Department of Pharmacy Services, Yale New Haven Hospital, New Haven, CT 06510, USA.

出版信息

Pharmacotherapy. 2012 Nov;32(11):e321-5. doi: 10.1002/phar.1132. Epub 2012 Oct 12.

Abstract

Vancomycin is a glycopeptide antibiotic used in the treatment of gram-positive infections including methicillin-resistant Staphylococcus aureus (MRSA). The most common adverse reaction to vancomycin is red man syndrome, which is a histaminergic reaction causing a rash on the upper torso, neck, and face after rapid infusion of the drug. Less commonly, vancomycin has been associated with thrombocytopenia. The etiology is believed to be the induction of drug-dependent antibodies, which in turn cause immune-mediated destruction of platelets. We describe a 41-year-old man who received two courses of vancomycin for the treatment of MRSA pneumonia and then experienced a decline in platelet count to a nadir of 15 x 10³/mm³. Vancomycin was discontinued, doxycycline was started, and the patient's platelet count rebounded over the next 6 days. The patient was readmitted to the hospital 2 months later for MRSA bacteremia and was rechallenged with vancomycin. He again experienced a decline in platelet count. Vancomycin was discontinued, and daptomycin was started. The patient's platelet count rebounded to normal levels over the next 5 days. Although the patient experienced acute thrombocytopenia after vancomycin exposure, no bleeding complications occurred, and the patient's platelet count rebounded to normal after the discontinuation of vancomycin. The patient had no other known risk factors for the development of rapid thrombocytopenia. Use of the Naranjo adverse drug reaction probability scale indicated a definite relationship (score of 9) between the patient's development of thrombocytopenia and vancomycin therapy. Although vancomycin was the presumed cause of thrombocytopenia in this patient, no drug-dependent antibody was isolated from blood samples collected after both exposures to vancomycin (analyzed by using a screening assay to identify drug-dependent antibodies to vancomycin [developed by the BloodCenter of Wisconsin]). Although the evidence supporting vancomycin induction of antibody-mediated destruction of platelets was lacking, further studies delineating alternate mechanisms of platelet destruction are warranted. Therefore, even in the absence of a positive antibody test, vancomycin should still be considered in the differential diagnosis as a cause of drug-induced thrombocytopenia.

摘要

万古霉素是一种糖肽类抗生素,用于治疗包括耐甲氧西林金黄色葡萄球菌 (MRSA) 在内的革兰氏阳性感染。万古霉素最常见的不良反应是红人综合征,这是一种组胺能反应,在药物快速输注后会在上半身、颈部和面部出现皮疹。不太常见的是,万古霉素与血小板减少症有关。病因被认为是诱导药物依赖性抗体,进而导致免疫介导的血小板破坏。我们描述了一名 41 岁男性,他因治疗 MRSA 肺炎接受了两疗程的万古霉素治疗,然后血小板计数下降至最低点 15 x 10³/mm³。停用万古霉素,开始使用多西环素,患者的血小板计数在接下来的 6 天内回升。两个月后,患者因 MRSA 菌血症再次入院,再次接受万古霉素治疗。他再次经历了血小板计数下降。停用万古霉素,开始使用达托霉素。患者的血小板计数在接下来的 5 天内回升至正常水平。尽管患者在接触万古霉素后出现急性血小板减少症,但没有发生出血并发症,并且在停用万古霉素后,患者的血小板计数恢复正常。患者没有其他已知的导致快速血小板减少症的危险因素。使用 Naranjo 药物不良反应概率量表表明,患者血小板减少症的发展与万古霉素治疗之间存在明确的关系(评分 9)。虽然在这名患者中,万古霉素被认为是血小板减少症的原因,但在两次接触万古霉素后从血液样本中未分离出药物依赖性抗体(通过使用威斯康星州血液中心开发的检测万古霉素药物依赖性抗体的筛选检测进行分析)。尽管缺乏支持万古霉素诱导抗体介导的血小板破坏的证据,但进一步研究阐明血小板破坏的替代机制是必要的。因此,即使没有阳性抗体检测结果,在鉴别诊断药物诱导的血小板减少症时,仍应考虑将万古霉素作为病因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验