• Bmc Infect Dis · Jan 2012

    Multicenter Study

    Development and validation of a bedside risk score for MRSA among patients hospitalized with complicated skin and skin structure infections.

    • Marya D Zilberberg, Paresh Chaudhari, Brian H Nathanson, Rebecca S Campbell, Matthew F Emons, Suzanne Fiske, Harlen D Hays, and Andrew F Shorr.
    • EviMed Research Group, LLC, Goshen, MA, USA. Evimedgroup@gmail.com
    • Bmc Infect Dis. 2012 Jan 1;12:154.

    BackgroundMethicillin-resistant Staphylococcus aureus (MRSA) is a frequent cause of complicated skin and skin structure infections (cSSSI). Patients with MRSA require different empiric treatment than those with non-MRSA infections, yet no accurate tools exist to aid in stratifying the risk for a MRSA cSSSI. We sought to develop a simple bedside decision rule to tailor empiric coverage more accurately.MethodsWe conducted a large multicenter (N=62 hospitals) retrospective cohort study in a US-based database between April 2005 and March 2009. All adult initial admissions with ICD-9-CM codes specific to cSSSI were included. Patients admitted with MRSA vs. non-MRSA were compared with regard to baseline demographic, clinical and hospital characteristics. We developed and validated a model to predict the risk of MRSA, and compared its performance via sensitivity, specificity and other classification statistics to the healthcare-associated (HCA) infection risk factors.ResultsOf the 7,183 patients with cSSSI, 2,387 (33.2%) had MRSA. Factors discriminating MRSA from non-MRSA were age, African-American race, no evidence of diabetes mellitus, cancer or renal dysfunction, and prior history of cardiac dysrhythmia. The score ranging from 0 to 8 points exhibited a consistent dose-response relationship. A MRSA score of 5 or higher was superior to the HCA classification in all characteristics, while that of 4 or higher was superior on all metrics except specificity.ConclusionsMRSA is present in 1/3 of all hospitalized cSSSI. A simple bedside risk score can help discriminate the risk for MRSA vs. other pathogens with improved accuracy compared to the HCA definition.

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