Kelly Sean G, Yarrington Michael, Zembower Teresa R, Sutton Sarah H, Silkaitis Christina, Postelnick Michael, Mikolajczak Anessa, Bolon Maureen K
1Vanderbilt University School of Medicine,Division of Infectious Diseases,Nashville,Tennessee.
2Northwestern Feinberg School of Medicine,Department of Medicine,Chicago,Illinois.
Infect Control Hosp Epidemiol. 2016 Dec;37(12):1395-1400. doi: 10.1017/ice.2016.210. Epub 2016 Sep 26.
BACKGROUND The nationally reported metric for Clostridium difficile infection (CDI) relies solely on laboratory testing, which can result in overreporting due to asymptomatic C. difficile colonization. OBJECTIVE To review the clinical scenarios of cases of healthcare facility-onset CDI (HO-CDI) and to determine the appropriateness of C. difficile testing on the basis of presence of symptomatic diarrhea in order to identify areas for improvement. DESIGN Retrospective cohort study. SETTING Northwestern Memorial Hospital, a large, tertiary academic hospital in Chicago, Illinois. PATIENTS The cohort included all patients with a positive C. difficile test result who were reported to the National Healthcare Safety Network as HO-CDI during a 1-year study period. METHODS We reviewed the clinical scenario of each HO-CDI case. On the basis of documentation and predefined criteria, appropriateness of C. difficile testing was determined; cases were deemed appropriate, inappropriate, or indeterminate. Statistical analysis was performed to compare demographic and clinical parameters among the categories of testing appropriateness. RESULTS Our facility reported 168 HO-CDI cases to NHSN during the study period. Of 168 cases, 33 (19.6%) were judged to be appropriate tests, 25 (14.8%) were considered inappropriate, and 110 (65.5%) were indeterminate. Elimination of inappropriate testing would have improved our facility's standardized infection ratio from 0.962 to 0.819. CONCLUSION Approximately 15% of HO-CDI cases were judged to be tested inappropriately. Testing only patients with clinically significant diarrhea would more accurately estimate CDI incidence, reduce unnecessary antibiotic use, and improve facilities' performance of reportable CDI metrics. Improved documentation could facilitate targeted interventions. Infect Control Hosp Epidemiol 2016;1395-1400.
全国报告的艰难梭菌感染(CDI)指标仅依赖实验室检测,这可能因无症状艰难梭菌定植导致报告过度。目的:回顾医疗机构获得性CDI(HO-CDI)病例的临床情况,并根据是否存在症状性腹泻来确定艰难梭菌检测的适宜性,以找出可改进之处。设计:回顾性队列研究。地点:伊利诺伊州芝加哥的大型三级学术医院西北纪念医院。患者:该队列包括在为期1年的研究期间被报告给国家医疗安全网络的所有艰难梭菌检测结果呈阳性的HO-CDI患者。方法:我们回顾了每例HO-CDI病例的临床情况。根据记录和预定义标准确定艰难梭菌检测的适宜性;病例被判定为适宜、不适宜或不确定。进行统计分析以比较检测适宜性类别之间的人口统计学和临床参数。结果:在研究期间,我们的机构向国家医疗安全网络报告了168例HO-CDI病例。在这168例病例中,33例(19.6%)被判定为检测适宜,25例(14.8%)被认为不适宜,110例(65.5%)不确定。消除不适当检测将使我们机构的标准化感染率从0.962提高到0.819。结论:约15%的HO-CDI病例被判定检测不当。仅对有临床显著腹泻的患者进行检测将更准确地估计CDI发病率,减少不必要的抗生素使用,并改善机构在可报告CDI指标方面的表现。改进记录有助于进行有针对性的干预。《感染控制与医院流行病学》2016年;1395 - 1400。