医学
万古霉素
败血症
血小板
弥漫性血管内凝血
肝素诱导血小板减少症
血栓性血小板减少性紫癜
内科学
免疫性血小板减少症
血小板减少性紫癜
胃肠病学
血液学
肝素
血小板输注
外科
金黄色葡萄球菌
生物
细菌
遗传学
作者
Shivani Shah,Ryan W. Sweeney,Maitreyee Rai,Deep Shah
标识
DOI:10.3390/hematolrep15020028
摘要
A male in his 60s presented with left lower extremity fractures following a vehicle accident. Hemoglobin, initially, was 12.4 mmol/L, and platelet count was 235 k/mcl. On day 11 of admission, his platelet count initially dropped to 99 k/mcl, and after recovery it rapidly decreased to 11 k/mcl on day 16 when the INR was 1.3 and aPTT was 32 s, and he continued to have a stable anemia throughout admission. There was no response in platelet count post-transfusion of four units of platelets. Hematology initially evaluated the patient for disseminated intravascular coagulation, heparin-induced thrombocytopenia (anti-PF4 antibody was 0.19), and thrombotic thrombocytopenic purpura (PLASMIC score of 4). Vancomycin was administered on days 1-7 for broad spectrum antimicrobial coverage and day 10, again, for concerns of sepsis. Given the temporal association of thrombocytopenia and vancomycin administration, a diagnosis of vancomycin-induced immune thrombocytopenia was established. Vancomycin was discontinued, and 2 doses of 1000 mg/kg of intravenous immunoglobulin 24 h apart were administered with the subsequent resolution of thrombocytopenia.
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