• Infect Control Hosp Epidemiol · Sep 2012

    Development of a modified surveillance definition of central line-associated bloodstream infections for patients with hematologic malignancies.

    • Megan J Digiorgio, Cynthia Fatica, Mary Oden, Brian Bolwell, Mikkael Sekeres, Matt Kalaycio, Patti Akins, Christina Shane, Jacob Bako, Steven M Gordon, and Thomas G Fraser.
    • Department of Infection Prevention, Quality and Patient Safety Institute, Cleveland, Ohio, USA. digiorm@ccf.org
    • Infect Control Hosp Epidemiol. 2012 Sep 1;33(9):865-8.

    ObjectiveTo develop a modified surveillance definition of central line-associated bloodstream infection (mCLABSI) specific for our population of patients with hematologic malignancies to better support ongoing improvement efforts at our hospital.DesignRetrospective cohort study.PatientsHematologic malignancies population in a 1,200-bed tertiary care hospital on a 22-bed bone marrow transplant (BMT) unit and a 22-bed leukemia unit.MethodsAn mCLABSI definition was developed, and pathogens and rates were compared against those determined using the National Healthcare Safety Network (NHSN) definition.ResultsBy the NHSN definition the CLABSI rate on the BMT unit was 6.0 per 1,000 central line-days, and by the mCLABSI definition the rate was 2.0 per 1,000 line-days ([Formula: see text]). On the leukemia unit, the NHSN CLABSI rate was 14.4 per 1,000 line-days, and the mCLABSI rate was 8.2 per 1,000 line-days ([Formula: see text]). The top 3 CLABSI pathogens by the NHSN definition were Enterococcus species, Klebsiella species, and Escherichia coli. The top 3 CLABSI pathogens by the mCLABSI definition were coagulase-negative Staphylococcus (CONS), Pseudomonas aeruginosa, and Staphylococcus aureus. The difference in the incidence of CONS as a cause of CLABSI under the 2 definitions was statistically significant ([Formula: see text]).ConclusionsA modified surveillance definition of CLABSI was associated with an increase in the identification of staphylococci as the cause of CLABSIs, as opposed to enteric pathogens, and a decrease in CLABSI rates.

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