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    Clinical and laboratory features of invasive community-onset methicillin-resistant Staphylococcus aureus infection: a prospective case-control study

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    Fulltext not available
    Authors
    Wehrhahn, M.
    Robinson, J.
    Pearson, J.
    O'Brien, Frances
    Tan, H.
    Coombs, Geoffrey
    Date
    2010
    Type
    Journal Article
    
    Metadata
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    Citation
    Wehrhahn, M.C. and Robinson, J.O. and Pearson, J.C. and O'Brien, F.G. and Tan, H.L. and Coombs, G.W. and Pascoe, E.M. and Lee, R. and Salvaris, P. and Salvaris, R. and New, D. and Murray, R.J. 2010. Clinical and laboratory features of invasive community-onset methicillin-resistant Staphylococcus aureus infection: a prospective case-control study. European Journal of Clinical Microbiology and Infectious Diseases. 29 (8): pp. 1025-1033.
    Source Title
    European Journal of Clinical Microbiology and Infectious Diseases
    DOI
    10.1007/s10096-010-0973-4
    ISSN
    09349723
    School
    School of Biomedical Sciences
    Remarks

    The original publication is available at: http://www.springerlink.com

    URI
    http://hdl.handle.net/20.500.11937/10275
    Collection
    • Curtin Research Publications
    Abstract

    and others - see citation for complete listing of authorsDifferences between the features of invasive community-onset methicillin-resistant Staphylococcus aureus (cMRSA) and methicillin-susceptible S. aureus (cMSSA) infections are incompletely understood. Fifty-seven patients with invasive cMRSA infection were prospectively identified at two teaching hospitals; for each cMRSA case, two cases of invasive cMSSA infection acted as controls. The primary outcome was 30-day all-cause mortality. Patients with invasive cMRSA infection were more likely to be Aboriginal (25% vs. 14%, age-adjusted odds ratio [OR] 2.5, p = 0.037), reside in a long-term care facility and/or have been hospitalised in the previous year (51% vs. 34%, p = 0.04) and less likely to have endocarditis (2% vs. 12%, p = 0.02) or require admission to an intensive care unit or high-dependency area (7% vs. 21%, p = 0.02).All-cause mortality at 30 days was similar in the cMRSA and cMSSA groups (9% vs. 7%, p = 0.68). Panton–Valentine leukocidin (PVL) genes were detected in a similar proportion of cMRSA and cMSSA isolates (32% vs. 27%, p = 0.49) and the presence of PVL genes was associated with younger age (35 years vs. 55 years, p < 0.001), Aboriginal ethnicity (38% vs. 10%, p < 0.001), skin and soft-tissue infection (54% vs. 19%, p < 0.001), lower illness severity at presentation (SAPS II score 9 vs. 21, p = 0.001) and shorter hospitalisation (9 days vs. 24 days, p < 0.001). Patients with “PVL-positive” and “PVL-negative” S. aureus infection had similar 30-day all-cause mortality (4% vs. 9%, p = 0.28). Few clinical features differentiated patients with invasive cMRSA infection from those with infection caused by cMSSA. Invasive “PVL-positive” S. aureus infection was associated with less morbidity but similar mortality to “PVL-negative” infection.

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