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Daptomycin For Intravenous Access-Related MRSA Septicemia: A Case Report

机译:达托霉素用于静脉通路相关的MRSA败血症:一例报告

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A 32-year-old black man receiving hemodialysis presented with intravenous access-related methicillin-resistant Staphylococcus aureus (possibly heterogenous vancomycin-intermediate S. aureus). He was successfully treated with daptomycin (minimum inhibitory concentration = 2 μg/mL) in spite of data from three laboratories suggesting the isolates were not susceptible to daptomycin. Introduction Dialysis patients have a 100-fold higher risk for invasive methicillin-resistant Staphylococcus aureus (MRSA) infections than the general population [1]. Resistant vancomycin-intermediate S. aureus (VISA) and heterogenous (h)VISA have been shown to be selected for by vancomycin exposure in patients with significant underlying illness, particularly chronic renal failure [2]. This case illustrates the limitations of current laboratory antibiotic susceptibility testing for MRSA with regard to the choice of effective therapy (figure). Case Presentation The patient, a 32-year-old black male, was admitted to our hospital August 13, 2008, with confusion, fever, and swelling of the upper right extremity. Septicemia from a right subclavian hemodialysis catheter was suspected. He had had the catheter since May 2008 and was on hemodialysis 3 times per week. Since July 2007, he had had recurrent vancomycin-susceptible S. aureus bacteremia and vascular access infections. His medical history included longstanding type 1 diabetes mellitus, a left below-the-knee amputation due to peripheral vascular disease, renal failure, hepatitis C, and AIDS (CD4 = 186 cells/μL). He had refused highly active antiretroviral therapy. In March 2008, he had had a subtotal gastrectomy due to a bleeding peptic ulcer.An ultrasound of the right upper extremity showed a deep venous thrombosis of the subclavian, axillary, and cephalic veins. Blood cultures from the hospital laboratory on August 13, 2008, grew a vancomycin-susceptible MRSA with a vancomycin minimum inhibitory concentration (MIC) of 2 μg/mL. He was started on vancomycin on August 13 at doses between 0.75 g and 1 g on hemodialysis. The subclavian catheter was removed on August 15, 2008, and replaced with a right femoral catheter. Cultures of the catheter tip and venipuncture blood cultures done the same day grew MRSA susceptible to vancomycin and linezolid, both with an MIC = 2 μg/mL. Daptomycin was not tested. He had received the 2 doses of vancomycin before repeat blood cultures (1 from venipuncture and 1 from the new femoral catheter) were obtained on August 20, 2008, which remained positive for MRSA. The local lab (Willis Knighton) referred the cultures to a reference lab (Focus) and the Centers for Disease Control (CDC) for daptomycin susceptibility testing. The results are given in table 1. He also received gentamicin at a dose of 80 mg on August 20 and 22, on hemodialysis. On August 20, 2008, while still on vancomycin, the patient was started on daptomycin at a dose of 6 mg/kg every 48 hours. On August 25, 2008, when the first daptomycin susceptibility results became available, the daptomycin MIC was 2 ug/mL, defined as non-susceptible, so linezolid was added to daptomycin. However, blood cultures from August 21 and 23, 2008, were both negative after 1 day of treatment with daptomycin and before the addition of linezolid. The patient was discharged from the hospital on September 3, 2008, and continued on both daptomycin and linezolid given after dialysis. He was readmitted to the hospital on September 8, 2008, with thrombocytopenia attributed to linezolid, which was discontinued. He remained on daptomycin as an inpatient on dialysis from September 10, 2008, through September 21, 2008. Figure. Summary of the treatment course and vancomycin and daptomycin minimum inhibitory concentrations (MICs) for methicillin-resistant Streptococcus aureus (MRSA) bloodstream and/or catheter tip isolates. +RFC, right femoral catheter inserted; -SCC, infected subclavian catheter removed, TCP, thrombocytopenia develops. Note: f
机译:一名接受血液透析的32岁黑人出现静脉注射相关耐甲氧西林的金黄色葡萄球菌(可能是异源万古霉素金黄色葡萄球菌)。尽管三个实验室的数据表明,分离株对达托霉素不敏感,但他仍成功接受达托霉素治疗(最低抑菌浓度= 2μg/ mL)。引言透析患者的侵袭性耐甲氧西林金黄色葡萄球菌(MRSA)感染的风险是普通人群的100倍[1]。已证明在患有严重基础疾病(尤其是慢性肾衰竭)的患者中,万古霉素暴露可抵抗耐药的万古霉素中间金黄色葡萄球菌(VISA)和异源性(h)VISA。该案例说明了在选择有效疗法方面,当前针对MRSA的实验室抗生素敏感性测试的局限性(图)。病例介绍该患者是一名32岁的黑人男性,于2008年8月13日因混乱,发烧和右上肢肿胀入院。怀疑来自右锁骨下血液透析导管的败血症。自2008年5月起,他开始使用导尿管,每周进行3次血液透析。自2007年7月以来,他患有万古霉素易感性金黄色葡萄球菌菌血症和血管通路感染。他的病史包括长期的1型糖尿病,由于周围血管疾病,肾衰竭,丙型肝炎和艾滋病(CD4 = 186细胞/μL)而导致的膝下截肢。他拒绝了高效的抗逆转录病毒疗法。 2008年3月,他因消化性溃疡出血而进行了胃大部切除术。右上肢超声检查发现锁骨下,腋窝和头静脉深静脉血栓形成。 2008年8月13日从医院实验室进行的血液培养产生了对万古霉素敏感的MRSA,其中万古霉素的最低抑菌浓度(MIC)为2μg/ mL。他于8月13日开始接受万古霉素的血液透析,剂量范围为0.75 g至1 g。锁骨下导管于2008年8月15日拆除,取而代之的是右股骨导管。当天进行的导管末端培养和静脉穿刺血培养使MRSA对万古霉素和利奈唑胺敏感,两者的MIC = 2μg/ mL。达托霉素未经测试。他于2008年8月20日获得了2剂万古霉素,然后进行了重复血液培养(1例来自静脉穿刺,1例来自新的股动脉导管),对MRSA仍然呈阳性反应。当地实验室(Willis Knighton)将培养物移交给参考实验室(Focus)和疾病控制中心(CDC)进行达托霉素敏感性测试。结果在表1中给出。他还于8月20日至22日接受血液透析的庆大霉素,剂量为80mg。 2008年8月20日,在仍使用万古霉素的同时,患者开始每48小时以6 mg / kg的剂量服用达托霉素。 2008年8月25日,当获得第一个达托霉素敏感性结果时,达托霉素MIC为2 ug / mL(定义为不敏感),因此将利奈唑胺添加到达托霉素中。但是,2008年8月21日至23日的血液培养物在达托霉素治疗1天后和加入利奈唑胺之前均呈阴性。该患者于2008年9月3日出院,透析后继续给予达托霉素和利奈唑胺治疗。他于2008年9月8日再次入院,其血小板减少症归因于利奈唑胺,已停药。从2008年9月10日到2008年9月21日,他一直在接受达托霉素透析治疗。治疗过程以及对耐甲氧西林的金黄色链球菌(MRSA)和/或导管尖端分离物的万古霉素和达托霉素的最低抑菌浓度(MIC)的摘要。 + RFC,右股动脉导管插入; -SCC,移除了感染的锁骨下导管,TCP,血小板减少。注意:f

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