从治疗尿路感染到粒细胞缺乏症。

IF 1 Q4 PRIMARY HEALTH CARE
Amit Katyal, Nikunj Tiwari, Vaka Rajshekhar, Maninder P S Pardal
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引用次数: 0

摘要

随着抗菌药物耐药性问题的日益严重,人们对磷霉素,尤其是磷霉素的肠外制剂越来越感兴趣。它是一种广谱抗生素,对多种细菌具有体内和体外活性,包括耐多药和XDR细菌。由于磷霉素的高组织穿透性,它可用于广泛的组织和靶标,包括中枢神经系统、软组织、骨、肺和脓肿液。最常见的不良反应是低钾血症和高钠血症。我们描述一个病例的粒细胞缺乏症在一个年轻的患者慢性肾脏疾病,一个罕见的副作用,可能是致命的。一名21岁的女性,因全身无力、食欲减退和高血压而被诊断为终末期肾病。她开始进行血液透析。住院期间,患者出现尿路感染特征,尿常规,镜检示白细胞酯酶3+和亚硝酸盐3+,镜检示大量脓细胞。血培养无菌。尿培养肺炎克雷伯菌(MDRO)阳性,仅对磷霉素敏感。开始口服磷霉素;然而,她在服用第一次口服剂量后出现多次恶心和呕吐。因此,她开始注射4 g磷霉素,随后每天两次注射2 g磷霉素。患者发现白细胞减少,在连续两天注射磷霉素后,白细胞总数从13500个/cumm下降到4100个/cumm,然后进一步下降到2100个/cumm。第3天,中性粒细胞计数进一步下降至1700个/μ m,绝对中性粒细胞计数为493个/μ。考虑到疑似磷霉素所致白细胞减少,停用该药。停用磷霉素2天后重复白细胞计数。重复白细胞计数正常。据我们所知,这是第一篇报道磷霉素引起慢性肾病患者粒细胞缺乏症的论文,也是迄今为止的第四篇。本文提供了一个案例的第二次详细描述。细胞毒性化疗可引起中性粒细胞计数的可预测和剂量相关的减少。继发于其他药物的中性粒细胞减少症往往是一种特异性反应,要么是免疫介导的反应,要么是因为直接的髓系损伤。这种效应与多种药物有关。文献资料很少。摘要产品的特点显示,只有少数病例的短暂中性粒细胞减少症和粒细胞缺乏症已被报道。肠外磷霉素常用于接受其他药物治疗的患者,因此它很少是唯一的怀疑。在我们的患者中,注射磷霉素治疗两天后,中性粒细胞计数突然下降,表明它是病原体。停药后计数恢复正常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From treating UTI to agranulocytosis.

The growing problem of antibacterial resistance has resulted in increased interest in fosfomycin, especially its parenteral formulation. It is a broad-spectrum antibiotic with both in vivo and in vitro activity against a wide range of bacteria, including MDR and XDR bacteria. Due to its high tissue penetration, fosfomycin may be used in a broad range of tissues and targets, including the CNS, soft tissue, bone, lungs, and abscess fluid. The most commonly reported adverse effects are hypokalemia and hypernatremia. We describe a case of agranulocytosis in a young patient with chronic kidney disease, a rarely described side effect that may be fatal. A 21-year-old woman was a freshly diagnosed case of end-stage renal disease during workup for complaints of generalized body weakness, reduced appetite, and hypertension. She was started on hemodialysis. During the course of her hospital stay, she developed features of urinary tract infection, urine routine and microscopy revealed leucocyte esterase 3+ and nitrites 3+ and microscopy showed numerous pus cells. The blood culture was sterile. The urine culture was positive for Klebsiella pneumoniae ssp pneumoniae (MDRO) and was sensitive to only fosfomycin. Oral fosfomycin was started; however, she developed multiple episodes of nausea and vomiting after taking the first oral dose. Therefore, she was started on 4 g of injectable fosfomycin, followed by 2 g of fosfomycin twice a day. She was found to have leukopenia, with her total leucocyte counts decreasing from 13500/cumm to 4100/cumm and then further to 2100 cells/cumm in two consecutive days of administration of injectable fosfomycin. On the third day, the counts further decreased to 1700/cumm, with an absolute neutrophil count of 493 cells/μ. In view of suspected fosfomycin-induced leukopenia, the injectable drug was stopped. The total leucocyte counts were repeated after two days of stopping fosfomycin. The repeated leucocyte counts were normal. To our knowledge, this is the first paper reporting on agranulocytosis induced by fosfomycin in chronic kidney disease patients and the fourth paper to date. This paper provides the second detailed description of a case. Cytotoxic chemotherapy can cause predictable and dose-related decreases in neutrophil counts. Neutropenia secondary to other medications tends to be an idiosyncratic reaction either as an immune-mediated reaction or because of direct myeloid cell line damage. This effect has been associated with a variety of medications. Literature data are scarce. A summary of product characteristics revealed that only a few cases of transient neutropenia and agranulocytosis have been reported. Parenteral fosfomycin is often used in patients receiving other medications, so it is rarely the only suspect. In our patient, there was a sudden decrease in the neutrophil count after two days of treatment with injectable fosfomycin, indicating that it is the causative agent. The counts normalized after stopping the drug.

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