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Daptomycin therapy for vancomycin-resistant enterococcus bacteremia in neutropenic patients with hematologic malignancies and hematopoietic cell transplantation recipients

机译:达托霉素治疗中性粒细胞减少症血液系统恶性肿瘤和造血细胞移植受者的万古霉素耐药肠球菌菌血症

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BACKGROUND: Vancomycin-resistant Enterococcus fascium (VRE) are rapidly emerging nosocomial pathogens in the United States and worldwide. Vancomycin resistance is recognized to be an independent risk factor for increased morbidity and mortality among patients with enterococcal bloodstream infections (BSI); thus, early appropriate therapy is vital in improving outcomes. We report our experience in treating VRE BSI in patients with hematologic malignancies with daptomycin, a cyclic lipopeptide antibiotic with bactericidal activity against VRE. METHODS: We performed retrospective chart review for patients with hematologic malignancies treated with daptomycin for a VRE BSI from January 2005 to May 2009. Patients were assessed for microbiological cure and survival. Patients were identified using a computerized clinical microbiology laboratory records. RESULTS: Of 74 patients with a VRE BSI, 40 patients (31 male patients; median age, 61 years) met criteria and were included in the study. In this series, 35.6% of the patients had received a hematopoietic stem cell transplant, and 57.8% of the patients were neutropenic. Vancomycin-resistant Enterococcus BSI occurred at a median of 20 days (4-109 days) of neutropenia among these patients. The patients were treated with daptomycin monotherapy (62.5%) or daptomycin plus other antimicrobial(s) (37.5%). For those who were successfully treated with daptomycin alone, the median duration of therapy was 9 days (1-36 days). Overall, 92.3% of the patients achieved a microbiological cure, which was evident at a median of 1 day (1-16 days) after the initiation of therapy. CONCLUSION: Daptomycin is an effective agent for the treatment of VRE BSI. For both daptomycin monotherapy or combination therapy, we would recommend an intravenous dose of 8 mg/kg once daily for 10 to 14 days.
机译:背景:耐万古霉素的肠球菌(VRE)是在美国和世界范围内迅速出现的医院内病原体。万古霉素耐药被认为是肠球菌血流感染(BSI)患者发病率和死亡率增加的独立危险因素;因此,早期的适当治疗对改善预后至关重要。我们报告了我们在治疗血液系统恶性肿瘤患者中使用达托霉素(一种对VRE具有杀菌活性的环状脂肽抗生素)治疗VRE BSI的经验。方法:我们对2005年1月至2009年5月接受达托霉素治疗VRE BSI的血液系统恶性肿瘤患者进行了回顾性图表回顾。评估了患者的微生物学治愈率和生存率。使用计算机化的临床微生物学实验室记录识别患者。结果:在74例VRE BSI患者中,有40例(31例男性;中位年龄为61岁)符合标准,被纳入研究。在该系列中,35.6%的患者接受了造血干细胞移植,而57.8%的患者为中性粒细胞减少。这些患者中,对万古霉素耐药的肠球菌BSI发生在中性粒细胞减少症的中位数为20天(4-109天)。患者接受达托霉素单药治疗(62.5%)或达托霉素加其他抗菌药物(37.5%)的治疗。对于仅使用达托霉素成功治疗的患者,中位治疗时间为9天(1-36天)。总体而言,92.3%的患者实现了微生物学治愈,这在开始治疗后的1天(1-16天)的中位数很明显。结论:达托霉素是治疗VRE BSI的有效药物。对于达托霉素单药治疗或联合治疗,我们建议静脉内剂量为8 mg / kg,每天一次,持续10至14天。

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