Clinical studyStaphylococcus aureus bacteremia: Current clinical patterns☆
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Cited by (203)
Hospital-acquired Staphylococcus aureus primary bloodstream infection: A comparison of events that do and do not meet the central line–associated bloodstream infection definition
2016, American Journal of Infection ControlCitation Excerpt :One reasonable assumption would be that non-CLABSIs are caused by a delay in diagnosis from an overlooked focus. A delay in recognition of infection has been considered a possible explanation because prior studies have shown an increase in complications, including endocarditis, with episodes of SA bacteremia with either an unknown portal of entry or community onset.11 Contrary to our findings, Fowler et al found long-term vascular access to be one risk for hematogenous complications from catheter-associated SA bloodstream infection.12
Optimizing antibiotic therapy of bacteremia and endocarditis due to staphylococci and enterococci: New insights and evidence from the literature
2015, Journal of Infection and ChemotherapyStaphylococcus aureus Bacteremia, Risk Factors, Complications, and Management
2013, Critical Care ClinicsCitation Excerpt :The absence of an obvious source of bacteremia has been shown to serve an important predictor of subsequent complications. In a series of 281 patients with SAB, the incidence of a metastatic complication was 2.5-fold lower with an identifiable source of bacteremia than among patients without an apparent source.3,7 The presence of prosthetic devices is frequently implicated as the source for SAB, as well as being an important risk factor for the development of complicated course, with mortality rates of up to 18% and a relapse rate of 15%.8
Infectious disease emergencies: Frontline clinical pearls
2012, Medical Clinics of North AmericaEndocarditis
2012, Critical Care Secrets: Fifth EditionClinical significance and outcome of polymicrobial Staphylococcus aureus bacteremia
2012, Journal of InfectionCitation Excerpt :Staphylococcus aureus is a frequent cause of bacteremia, and S. aureus bacteremia (SAB) is associated with high rates of life threatening complications, with documented associated mortality rates of 20–40%.9,10 Polymicrobial SAB has been observed in 2–17% of patients with SAB.11,12 Although several studies have assessed patients with polymicrobial bacteremia,1,3–7,13–16 none, to our knowledge, has focused on polymicrobial SAB.
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This study was supported by Grant AI03456 from the National Institute of Allergy and Infectious Disease. This study was presented in part at the Annual Session of the American College of Physicians, San Francisco, California, April, 1975.
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Present address: Department of Medicine, University of Arkansas Medical Center, Little Rock, Arkansas 72201.
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From the Department of Medicine, University of Washington, Seattle, Washington.