Division of Hematology/Oncology, Department of Medicine, University of Florida, Gainesville, FL, USA.
Ann Pharmacother. 2012 Jan;46(1):e1. doi: 10.1345/aph.1Q467. Epub 2011 Dec 13.
To report a case of severe neutropenia after discontinuing prolonged treatment with vancomycin that progressed to agranulocytosis with vancomycin reexposure.
A 78-year-old woman presented with severe neutropenia (absolute neutrophil count [ANC] 37 cells/μL) and hypocellular bone marrow with absence of myeloid elements 8 weeks after discontinuing a 3-week treatment course of vancomycin 750 mg every 12 hours. Filgrastim 300 μg daily was started for neutropenia and vancomycin 750 mg every 12 hours and aztreonam 1 g every 8 hours were initiated for catheter-related acute thrombophlebitis of the upper extremity. The patient's ANC decreased to 10 cells/μL within 3 days of starting vancomycin. We suspected an autoimmune process, potentially related to vancomycin exposure, and began treatment with methylprednisolone 1 mg/kg daily. The ANC precipitously dropped to 0 cells/μL despite treatment with steroids and an increased filgrastim dose of 480 μg/day. All antibiotics were discontinued on the fifth day of hospitalization. Within 48 hours, her neutrophil count showed recovery (white blood cell count 500 cells/μL; 10% neutrophils).
Idiosyncratic drug-induced agranulocytosis is an uncommon phenomenon but is often associated with serious consequences such as sepsis. We believe this case is unique because of the unusually late neutropenia discovered several weeks after finishing a prolonged course of vancomycin. Furthermore, agranulocytosis developed after unintentional rechallenge with vancomycin. According to the Naranjo probability scale, this case illustrates a probable adverse event caused by vancomycin.
This case demonstrates a serious adverse event potentially associated with vancomycin use, and calls attention to the safety of rechallenging with vancomycin during a possible drug-induced neutropenia.
报告 1 例因停止万古霉素长期治疗而导致严重中性粒细胞减少症(中性粒细胞绝对计数 [ANC] 37 个/μL),并在再次接触万古霉素后进展为粒细胞缺乏症的病例。
1 名 78 岁女性,在停止万古霉素 750mg 每 12 小时治疗 3 周后 8 周时出现严重中性粒细胞减少症(ANC 37 个/μL)和骨髓细胞减少,无髓细胞成分。为治疗中性粒细胞减少症,开始每日皮下注射 300μg 非格司亭;因上肢导管相关性急性血栓性静脉炎,开始每日静脉滴注 750mg 万古霉素和每 8 小时 1g 氨曲南。开始万古霉素治疗后 3 天内,患者的 ANC 降至 10 个/μL。我们怀疑这是一种自身免疫过程,可能与万古霉素暴露有关,并开始每日 1mg/kg 静脉滴注甲泼尼龙治疗。尽管给予类固醇和增加非格司亭剂量至 480μg/天,但 ANC 急剧下降至 0 个/μL。住院第 5 天停用所有抗生素。在 48 小时内,她的中性粒细胞计数恢复(白细胞计数 500 个/μL;10%为中性粒细胞)。
药物诱导的特发性粒细胞缺乏症是一种罕见现象,但常伴有严重后果,如败血症。我们认为,这个病例很独特,因为在停止长时间使用万古霉素数周后,发现了异常迟发性中性粒细胞减少症。此外,在无意中再次接触万古霉素后发生了粒细胞缺乏症。根据 Naranjo 概率量表,本例说明可能与万古霉素有关的严重不良事件。
本病例表明,与万古霉素使用相关的潜在严重不良事件,提示在可能的药物诱导性中性粒细胞减少症期间,再次使用万古霉素需要注意安全性。