万古霉素致严重免疫性血小板减少症1例。

IF 1.1 Q4 HEMATOLOGY Hematology Reports Pub Date : 2023-04-24 DOI:10.3390/hematolrep15020028
Shivani Shah, Ryan Sweeney, Maitreyee Rai, Deep Shah
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引用次数: 0

摘要

一名60多岁的男性因车祸左下肢骨折。血红蛋白最初为12.4 mmol/L,血小板计数为235 k/mcl。入院第11天,患者血小板计数最初降至99 k/mcl,恢复后迅速降至11 k/mcl,第16天INR为1.3,aPTT为32 s,入院期间患者贫血情况持续稳定。输注4单位血小板后,血小板计数无反应。血液学初步评估患者的弥散性血管内凝血、肝素诱导的血小板减少症(抗pf4抗体为0.19)和血栓性血小板减少性紫癜(PLASMIC评分为4)。在第1-7天给予万古霉素,以获得广谱抗菌覆盖,第10天再次给予万古霉素,以防止败血症。鉴于血小板减少与万古霉素给药的时间相关性,建立了万古霉素诱导的免疫性血小板减少的诊断。万古霉素停用,间隔24小时静脉注射免疫球蛋白2次,每次1000 mg/kg,随后血小板减少症消退。
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A Case of Vancomycin-Induced Severe Immune Thrombocytopenia.

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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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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