Reisner B S, Shaw S, Huber M E, Woodmansee C E, Costa S, Falk P S, Mayhall C G
Department of Pathology, University of Texas Medical Branch at Galveston, USA.
Infect Control Hosp Epidemiol. 2000 Dec;21(12):775-9. doi: 10.1086/501734.
To establish an efficient and sensitive technique for recovering vancomycin-resistant enterococci (VRE) from perianal and environmental samples collected during implementation of control measures for an outbreak of VRE.
Perianal and environmental samples were collected in triplicate on sterile swabs. One swab was used to inoculate a selective broth medium containing 6 pg of vancomycin and 8 pg of ciprofloxacin per mL, one to inoculate Campylobacter agar containing 10 microg/mL of vancomycin, and one to inoculate Enterococcosel agar containing 8 microg/mL of vancomycin.
Samples were collected in the intensive care units of a 600-bed university hospital over a period of 2 months. SAMPLE SELECTION: Patients and their immediate environment were sampled if they resided in a ward with a patient known to be colonized or infected with VRE.
Of the 88 perianal samples obtained from 63 patients, 37 were positive for VRE by broth culture, with 36 also recovered on both types of solid media (sensitivity, 97.3%; negative predictive value, 98.1%). Of the initial samples collected from each of the 63 patients, 20 were positive for VRE by all methods. Of the 500 environmental samples cultured, 139 were positive for VRE in broth, with only 33 recovered on Campylobacter agar (sensitivity, 23.7%; negative predictive value, 77.2%) and 22 on Enterococcosel agar (sensitivity, 15.8%; negative predictive value, 75.2%).
Our data indicate that, when performing surveillance cultures during an outbreak of VRE, use of an enrichment broth medium is required to recover VRE contaminating environmental surfaces; however, direct inoculation to selective solid medium is adequate to recover VRE in patient perianal specimens.
建立一种高效且灵敏的技术,用于从耐万古霉素肠球菌(VRE)暴发控制措施实施期间采集的肛周和环境样本中分离出VRE。
用无菌拭子对肛周和环境样本进行一式三份采集。一份拭子接种于每毫升含6微克万古霉素和8微克环丙沙星的选择性肉汤培养基,一份接种于每毫升含10微克万古霉素的弯曲菌琼脂,一份接种于每毫升含8微克万古霉素的肠球菌琼脂。
在一家拥有600张床位的大学医院的重症监护病房,在2个月的时间内采集样本。
如果患者居住在有已知感染或定植VRE患者的病房,则对患者及其直接环境进行采样。
从63名患者获得的88份肛周样本中,37份经肉汤培养VRE呈阳性,其中36份在两种固体培养基上也培养出VRE(灵敏度为97.3%;阴性预测值为98.1%)。在63名患者各自最初采集的样本中,20份通过所有方法检测VRE均呈阳性。在培养的500份环境样本中,139份经肉汤培养VRE呈阳性,在弯曲菌琼脂上仅培养出33份(灵敏度为23.7%;阴性预测值为77.2%),在肠球菌琼脂上培养出22份(灵敏度为15.8%;阴性预测值为75.2%)。
我们的数据表明,在VRE暴发期间进行监测培养时,需要使用增菌肉汤培养基来分离污染环境表面的VRE;然而,直接接种到选择性固体培养基足以从患者肛周标本中分离出VRE。