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哌拉西林和万古霉素引起住院患者严重血小板减少症。

Piperacillin and vancomycin induced severe thrombocytopenia in a hospitalized patient.

机构信息

Mercy Medical Center, Cedar Rapids, Iowa, USA.

出版信息

Platelets. 2011;22(4):294-301. doi: 10.3109/09537104.2010.549973. Epub 2011 Feb 10.

DOI:10.3109/09537104.2010.549973
PMID:21309645
Abstract

In hospitalized patients with complex medical problems on numerous drugs, thrombocytopenia may have a multiple confounding etiology. Keeping this in mind, it is of utmost importance to monitor the platelet count regularly during hospitalization and on subsequent follow-up visits, even after the most probable etiology has been identified/most likely causative drug has been withdrawn. Isolated thrombocytopenia with no evidence of microangiopathic hemolysis on the peripheral blood smear in an acutely ill hospitalized patient implicated sepsis, disseminated intravascular coagulation and drugs as the most probable causes. Our patient represents an uncommon case of antibiotic-induced severe immune thrombocytopenia, as he developed both vancomycin-dependent and piperacillin-dependent antibodies, while being treated for cellulitis (vancomycin-specific antibodies of the IgG isotype, and both IgG and IgM antibodies specific for piperacillin were identified in laboratory testing). Vancomycin was stopped before the reports were available. Following this, the patient's platelet count showed a transient upward trend, but then the thrombocytopenia worsened drastically reaching a nadir of 10,000/µL. The platelet count returned to normal only after piperacillin/tazobactam was stopped after a week, thus establishing it as the cause of the more severe thrombocytopenia, which occurred later on; this was subsequently confirmed by the laboratory results. Vancomycin is an established cause of drug-induced immune thrombocytopenias, especially in acutely ill, hospitalized or elderly patients, whereas incidents of piperacillin/tazobactam-induced immune thrombocytopenia are uncommon. In case clinical suspicion is high, workup should include immunoprecipitation and flow cytometry studies to confirm antiplatelet antibodies.

摘要

在患有多种药物复杂医学问题的住院患者中,血小板减少症可能有多种混杂病因。考虑到这一点,在住院期间和随后的随访期间,即使已经确定了最可能的病因/最可能的致病药物并已停用,定期监测血小板计数非常重要。在患有严重疾病的住院患者中,如果外周血涂片没有微血管病性溶血性贫血的证据,孤立性血小板减少症提示最可能的病因是感染性休克、弥散性血管内凝血和药物。我们的患者代表了一种不常见的抗生素诱导的严重免疫性血小板减少症病例,因为他在治疗蜂窝织炎时同时产生了依赖万古霉素和依赖哌拉西林的抗体(实验室检测中鉴定出 IgG 同种型的万古霉素特异性抗体,以及针对哌拉西林的 IgG 和 IgM 抗体)。在报告出来之前停用了万古霉素。此后,患者的血小板计数短暂上升,但随后血小板减少症急剧恶化,血小板计数降至 10,000/µL。仅在停用哌拉西林/他唑巴坦一周后,血小板计数才恢复正常,从而确定其为更严重的血小板减少症的原因,这种情况随后在实验室结果中得到了证实。万古霉素是药物诱导免疫性血小板减少症的既定原因,尤其是在患有严重疾病、住院或老年患者中,而哌拉西林/他唑巴坦引起免疫性血小板减少症的情况则不常见。如果临床怀疑很高,应进行包括免疫沉淀和流式细胞术研究以确认抗血小板抗体的检查。

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