Clinical Microbiology, Laboratory Medicine, University Hospital Basel, Basel, Switzerland; Applied Microbiology Research, Department Biomedicine, University of Basel, Switzerland.
Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland.
Clin Microbiol Infect. 2017 Feb;23(2):118.e1-118.e7. doi: 10.1016/j.cmi.2016.10.003. Epub 2016 Oct 13.
In this study we aimed to analyse the association between use of daptomycin and MICs of daptomycin in Enterococcus faecium bacteraemia.
We prospectively enrolled patients aged ≥18 years with E. faecium bacteraemia hospitalized at the University Hospital Basel from 2008 to 2014. We determined daptomycin MICs by Etests and used pulsed field gel electrophoresis to determine clonal relatedness. We recorded the defined daily dosages of daptomycin (DDDs) per 100 patient-days and clinical data from charts. We correlated daptomycin MIC with use of daptomycin in patients with recurrence/persistence.
In 195 E. faecium bacteraemias originating from 162 patients the median MIC for daptomycin was 2 mg/L (IQR 2-3); 30% (15.4%) isolates had a MIC ≥4 mg/L and 6 (3.1%) were resistant (MIC >4 mg/L) according to CLSI criteria. The usage of daptomycin increased more than four-fold from 0.36 DDDs/100 patient-days in 2008 to 1.6 in 2014. In 13 of 28 (42.9%) patients with a relapsing or persisting bacteraemia, the daptomycin MIC of the second isolate increased from a median of 2.0 to 2.5 mg/L (p 0.010); 3/13 (23.1%) developed resistance. All patients with the same clone in the first and second episode and an increase of daptomycin MIC had been treated with daptomycin (6/6 versus 1/7 p 0.005).
Daptomycin MICs and Daptomycin usage increased over time. On an individual patient level daptomycin exposure was associated with an increased MIC in subsequent bacteraemia episodes. Diversity did not indicate a clonal origin and argues for a de novo development of resistance.
本研究旨在分析屎肠球菌菌血症患者使用达托霉素与达托霉素 MIC 值之间的相关性。
我们前瞻性地招募了 2008 年至 2014 年期间在巴塞尔大学医院住院的年龄≥18 岁的屎肠球菌菌血症患者。我们通过 Etest 确定达托霉素 MIC 值,并使用脉冲场凝胶电泳来确定克隆相关性。我们从图表中记录了每位患者每天的达托霉素定义日剂量(DDD)和临床数据。我们将达托霉素 MIC 值与复发/持续患者的达托霉素使用情况进行了相关分析。
在 162 例患者的 195 例屎肠球菌菌血症中,达托霉素的中位 MIC 值为 2mg/L(IQR 2-3);根据 CLSI 标准,30%(15.4%)的分离株 MIC 值≥4mg/L,6 株(3.1%)为耐药(MIC>4mg/L)。2008 年达托霉素的使用量为 0.36 DDDs/100 患者-天,到 2014 年增加了四倍多。在 28 例复发或持续菌血症患者中有 13 例(42.9%),第二次分离株的达托霉素 MIC 值从中位数 2.0 增加到 2.5mg/L(p=0.010);3/13(23.1%)出现耐药。第一次和第二次发作中具有相同克隆且达托霉素 MIC 值增加的所有患者均接受了达托霉素治疗(6/6 与 1/7,p=0.005)。
达托霉素 MIC 值和达托霉素的使用随着时间的推移而增加。在个体患者层面,达托霉素的暴露与随后的菌血症发作中 MIC 值的增加有关。多样性并不能表明克隆起源,并表明新出现的耐药性。