Bush Kathryn, Leal Jenine, Fathima Sumana, Li Vincent, Vickers David, Chui Linda, Louie Marie, Taylor Geoffrey, Henderson Elizabeth
Infection Prevention and Control, Alberta Health Services, Calgary, AB Canada.
Alberta Provincial Laboratory for Public Health, Edmonton and Calgary, AB Canada.
Antimicrob Resist Infect Control. 2015 Sep 14;4:35. doi: 10.1186/s13756-015-0076-1. eCollection 2015.
Infection Prevention and Control (IPC) surveillance for incident methicillin-resistant Staphylococcus aureus (MRSA) in hospitalized patients is performed in a complete provincial surveillance network of all acute care facilities in Alberta, Canada. IPC surveillance is centralized using a web-based data entry platform so that each patient is counted only once. All diagnostic laboratories submit the first clinical MRSA isolate associated with a patient without previous MRSA positive clinical cultures in the preceding year to the Provincial Laboratory for Public Health (ProvLab) for molecular typing. This study will investigate the relationship between the IPC epidemiological classification based on time of detection following admission to hospital (Hospital Acquired and Community Associated) and the matched laboratory MRSA surveillance data using a retrospective cohort study design.
Incident IPC MRSA cases were classified according to IPC epidemiologic definitions. DNA sequencing of the Staphylococcus protein A (spa) gene and pulsed-field gel electrophoresis (PFGE) typing was performed. IPC MRSA surveillance data were matched to the ProvLab molecular surveillance data. Univariate comparisons of proportions were performed for categorical variables and the Student's t test for continuous variables.
MRSA molecular typing data were available for matching for 46.7 % (2248/4818) of incident IPC cases. There was agreement in definitions for traditional nosocomial clones (USA100/CMRSA2) with Hospital Acquired (HA)-MRSA (65.1 % of all IPC HA-MRSA) and traditional community clones (USA400/CMRSA7 and USA300/CMRSA10) with Community Acquired (CA)-MRSA (62.4 % of CA-MRSA). However, we observed discordance for both traditional nosocomial/CA-MRSA (30.4 % of CA-MRSA) and for traditional community/HA-MRSA (26.9 % of HA-MRSA).
We note agreement between traditional nosocomial clones and HA-MRSA, and traditional community clones and CA-MRSA. However, approximately one-quarter of HA-MRSA are those of traditional community clones while approximately one-third of CA-MRSA are those of traditional nosocomial clones. Collaborative provincial MRSA surveillance is important as the distinction between IPC case attribution in acute care settings and the historical definitions of MRSA clones as community- or healthcare-associated have blurred.
加拿大艾伯塔省所有急症护理机构组成的完整省级监测网络,对住院患者新发耐甲氧西林金黄色葡萄球菌(MRSA)进行感染预防与控制(IPC)监测。IPC监测通过基于网络的数据录入平台集中进行,从而使每位患者仅被计数一次。所有诊断实验室将与前一年无MRSA阳性临床培养结果的患者相关的首例临床MRSA分离株提交给省级公共卫生实验室(ProvLab)进行分子分型。本研究将采用回顾性队列研究设计,调查基于入院后检测时间的IPC流行病学分类(医院获得性和社区相关性)与匹配的实验室MRSA监测数据之间的关系。
新发IPC MRSA病例根据IPC流行病学定义进行分类。进行葡萄球菌蛋白A(spa)基因的DNA测序和脉冲场凝胶电泳(PFGE)分型。将IPC MRSA监测数据与ProvLab分子监测数据进行匹配。对分类变量进行比例的单因素比较,对连续变量进行学生t检验。
46.7%(2248/4,818)的新发IPC病例有可供匹配的MRSA分子分型数据。传统医院克隆株(USA100/CMRSA2)与医院获得性(HA)-MRSA(占所有IPC HA-MRSA的65.1%)以及传统社区克隆株(USA400/CMRSA7和USA300/CMRSA10)与社区获得性(CA)-MRSA(占CA-MRSA的62.4%)在定义上存在一致性。然而,我们观察到传统医院/CA-MRSA(占CA-MRSA的30.4%)以及传统社区/HA-MRSA(占HA-MRSA的26.9%)均存在不一致性。
我们注意到传统医院克隆株与HA-MRSA、传统社区克隆株与CA-MRSA之间存在一致性。然而,约四分之一的HA-MRSA属于传统社区克隆株,而约三分之一的CA-MRSA属于传统医院克隆株。由于急症护理环境中IPC病例归因与MRSA克隆株作为社区相关或医疗保健相关的历史定义之间的区别已经模糊,省级协作的MRSA监测很重要。