The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia

<p>Abstract</p> <p>Background</p> <p>Management of methicillin-resistant <it>Staphylococcus aureus </it>(MRSA) bacteremia remains a challenge. The emergence of MRSA strains with reduced vancomycin susceptibility complicates treatment.</p> <p>Meth...

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Main Authors: Honda Hitoshi, Doern Christopher D, Michael-Dunne Wm, Warren David K
Format: Article
Language:English
Published: BMC 2011-12-01
Series:BMC Infectious Diseases
Online Access:http://www.biomedcentral.com/1471-2334/11/335
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spelling doaj-6d04af7ca24b44bb99465a76cdd460a52020-11-25T03:39:13ZengBMCBMC Infectious Diseases1471-23342011-12-0111133510.1186/1471-2334-11-335The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremiaHonda HitoshiDoern Christopher DMichael-Dunne WmWarren David K<p>Abstract</p> <p>Background</p> <p>Management of methicillin-resistant <it>Staphylococcus aureus </it>(MRSA) bacteremia remains a challenge. The emergence of MRSA strains with reduced vancomycin susceptibility complicates treatment.</p> <p>Methods</p> <p>A prospective cohort study (2005-2007) of patients with MRSA bacteremia treated with vancomycin was performed at an academic hospital. Vancomycin minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined for stored MRSA isolates. Cox regression analysis was performed to predict 28-day all-cause mortality.</p> <p>Results</p> <p>One hundred sixty-three patients with MRSA bacteremia were evaluated. One hundred twelve patients (68.7%) had bacteremia due to MRSA with a vancomycin MIC ≥ 2 <it>ug</it>/mL. Among strains with a vancomycin MIC ≥ 2 <it>ug</it>/mL, 10 isolates (8.9%) were vancomycin-intermediate <it>S. aureus </it>(VISA). Thirty-five patients (21.5%) died within 28 days after the diagnosis of MRSA bacteremia. Higher vancomycin MIC was not associated with mortality in this cohort [adjusted hazard ratio (aHR), 1.57; 95% confidence interval (CI), 0.73-3.37]. Vancomycin tolerance was observed in 4.3% (7/162) of isolates and was not associated with mortality (crude HR, 0.62; 95% CI, 0.08-4.50). Factors independently associated with mortality included higher age (aHR, 1.03; 95% CI 1.00-1.05), cirrhosis (aHR, 3.01; 95% CI, 1.24-7.30), and intensive care unit admission within 48 hours after the diagnosis of bacteremia (aHR, 5.99; 95% CI, 2.86-12.58).</p> <p>Conclusions</p> <p>Among patients with MRSA bacteremia treated with vancomycin, reduced vancomycin susceptibility and vancomycin tolerance were not associated with mortality after adjusting for patient factors. Patient factors including severity of illness and underlying co-morbidities were associated with the mortality.</p> http://www.biomedcentral.com/1471-2334/11/335
collection DOAJ
language English
format Article
sources DOAJ
author Honda Hitoshi
Doern Christopher D
Michael-Dunne Wm
Warren David K
spellingShingle Honda Hitoshi
Doern Christopher D
Michael-Dunne Wm
Warren David K
The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia
BMC Infectious Diseases
author_facet Honda Hitoshi
Doern Christopher D
Michael-Dunne Wm
Warren David K
author_sort Honda Hitoshi
title The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia
title_short The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia
title_full The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia
title_fullStr The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia
title_full_unstemmed The impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>Staphylococcus aureus </it>bacteremia
title_sort impact of vancomycin susceptibility on treatment outcomes among patients with methicillin resistant <it>staphylococcus aureus </it>bacteremia
publisher BMC
series BMC Infectious Diseases
issn 1471-2334
publishDate 2011-12-01
description <p>Abstract</p> <p>Background</p> <p>Management of methicillin-resistant <it>Staphylococcus aureus </it>(MRSA) bacteremia remains a challenge. The emergence of MRSA strains with reduced vancomycin susceptibility complicates treatment.</p> <p>Methods</p> <p>A prospective cohort study (2005-2007) of patients with MRSA bacteremia treated with vancomycin was performed at an academic hospital. Vancomycin minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined for stored MRSA isolates. Cox regression analysis was performed to predict 28-day all-cause mortality.</p> <p>Results</p> <p>One hundred sixty-three patients with MRSA bacteremia were evaluated. One hundred twelve patients (68.7%) had bacteremia due to MRSA with a vancomycin MIC ≥ 2 <it>ug</it>/mL. Among strains with a vancomycin MIC ≥ 2 <it>ug</it>/mL, 10 isolates (8.9%) were vancomycin-intermediate <it>S. aureus </it>(VISA). Thirty-five patients (21.5%) died within 28 days after the diagnosis of MRSA bacteremia. Higher vancomycin MIC was not associated with mortality in this cohort [adjusted hazard ratio (aHR), 1.57; 95% confidence interval (CI), 0.73-3.37]. Vancomycin tolerance was observed in 4.3% (7/162) of isolates and was not associated with mortality (crude HR, 0.62; 95% CI, 0.08-4.50). Factors independently associated with mortality included higher age (aHR, 1.03; 95% CI 1.00-1.05), cirrhosis (aHR, 3.01; 95% CI, 1.24-7.30), and intensive care unit admission within 48 hours after the diagnosis of bacteremia (aHR, 5.99; 95% CI, 2.86-12.58).</p> <p>Conclusions</p> <p>Among patients with MRSA bacteremia treated with vancomycin, reduced vancomycin susceptibility and vancomycin tolerance were not associated with mortality after adjusting for patient factors. Patient factors including severity of illness and underlying co-morbidities were associated with the mortality.</p>
url http://www.biomedcentral.com/1471-2334/11/335
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