Predictive factors for mortality in patients with methicillin‐resistant Staphylococcus aureus bloodstream infection: impact on outcome of host, microorganism and therapy. (17th January 2013)
- Record Type:
- Journal Article
- Title:
- Predictive factors for mortality in patients with methicillin‐resistant Staphylococcus aureus bloodstream infection: impact on outcome of host, microorganism and therapy. (17th January 2013)
- Main Title:
- Predictive factors for mortality in patients with methicillin‐resistant Staphylococcus aureus bloodstream infection: impact on outcome of host, microorganism and therapy
- Authors:
- Gasch, O.
Camoez, M.
Dominguez, M. A.
Padilla, B.
Pintado, V.
Almirante, B.
Molina, J.
Lopez‐Medrano, F.
Ruiz, E.
Martinez, J. A.
Bereciartua, E.
Rodriguez‐Lopez, F.
Fernandez‐Mazarrasa, C.
Goenaga, M. A.
Benito, N.
Rodriguez‐Baño, J.
Espejo, E.
Pujol, M.
Lina, G. - Abstract:
- <abstract abstract-type="main" id="clm12106-abs-0001"> <title>Abstract</title> <p>Mortality related to methicillin‐resistant <italic>Staphylococcus aureus</italic> (MRSA) bloodstream infection (BSI) remains high, despite changes in the epidemiology. To analyze the current predictive factors for mortality we conducted a prospective study in a large cohort of patients with MRSA‐BSI from 21 Spanish hospitals. Epidemiology, clinical data, therapy and outcome were recorded. All MRSA strains were analysed, including susceptibility to antibiotics and molecular characterization. Vancomycin MICs (V‐MIC) were tested by the <italic>E</italic>‐test and microdilution methods. Time until death was the dependent variable in a Cox regression analysis. Overall, 579 episodes were included. Acquisition was nosocomial in 59% and vascular catheter was the most frequent source (38%). A dominant PFGE genotype was found in 368 (67%) isolates, which belonged to Clonal Complex (CC)5 and carried SCCmecIV and <italic>agr2</italic>. Microdilution V‐MIC50 and V‐MIC90 were 0.7 and 1.0 mg/L, respectively. Initial therapy was appropriate in 66% of episodes. Overall mortality was observed in 179 (32%) episodes. The Cox‐regression analysis identified age &gt;70 years (HR 1.88), previous fatal disease (HR 2.16), Pitt score &gt;1 (HR 3.45), high‐risk source (HR 1.85) and inappropriate initial treatment (HR 1.39) as independent predictive factors for mortality. CC5 and CC22 (HR 0.52 and 0.45) were associated<abstract abstract-type="main" id="clm12106-abs-0001"> <title>Abstract</title> <p>Mortality related to methicillin‐resistant <italic>Staphylococcus aureus</italic> (MRSA) bloodstream infection (BSI) remains high, despite changes in the epidemiology. To analyze the current predictive factors for mortality we conducted a prospective study in a large cohort of patients with MRSA‐BSI from 21 Spanish hospitals. Epidemiology, clinical data, therapy and outcome were recorded. All MRSA strains were analysed, including susceptibility to antibiotics and molecular characterization. Vancomycin MICs (V‐MIC) were tested by the <italic>E</italic>‐test and microdilution methods. Time until death was the dependent variable in a Cox regression analysis. Overall, 579 episodes were included. Acquisition was nosocomial in 59% and vascular catheter was the most frequent source (38%). A dominant PFGE genotype was found in 368 (67%) isolates, which belonged to Clonal Complex (CC)5 and carried SCCmecIV and <italic>agr2</italic>. Microdilution V‐MIC50 and V‐MIC90 were 0.7 and 1.0 mg/L, respectively. Initial therapy was appropriate in 66% of episodes. Overall mortality was observed in 179 (32%) episodes. The Cox‐regression analysis identified age &gt;70 years (HR 1.88), previous fatal disease (HR 2.16), Pitt score &gt;1 (HR 3.45), high‐risk source (HR 1.85) and inappropriate initial treatment (HR 1.39) as independent predictive factors for mortality. CC5 and CC22 (HR 0.52 and 0.45) were associated with significantly lower mortality rates than CC8. V‐MIC ≥1.5 did not have a significant impact on mortality, regardless of the method used to assess it.</p> </abstract> … (more)
- Is Part Of:
- Clinical microbiology and infection. Volume 19:Number 11(2013:Nov.)
- Journal:
- Clinical microbiology and infection
- Issue:
- Volume 19:Number 11(2013:Nov.)
- Issue Display:
- Volume 19, Issue 11 (2013)
- Year:
- 2013
- Volume:
- 19
- Issue:
- 11
- Issue Sort Value:
- 2013-0019-0011-0000
- Page Start:
- 1049
- Page End:
- 1057
- Publication Date:
- 2013-01-17
- Subjects:
- Medical microbiology -- Periodicals
Diagnostic microbiology -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
616.01 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-0691 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1469-0691.12108 ↗
- Languages:
- English
- ISSNs:
- 1198-743X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.305520
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3981.xml