Literature DB >> 17243049

A prospective investigation of outcomes after hospital discharge for endemic, community-acquired methicillin-resistant and -susceptible Staphylococcus aureus skin infection.

Loren G Miller1, Clifford Quan, Anthony Shay, Katayoun Mostafaie, Kiran Bharadwa, Nelly Tan, Kelli Matayoshi, Jason Cronin, Jennifer Tan, Grace Tagudar, Arnold S Bayer.   

Abstract

BACKGROUND: Although community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) infection has become increasingly common, prospective data on outcomes of patients with skin infection remain poorly defined.
METHODS: We prospectively observed a cohort of 201 patients discharged after hospitalization for CA-MRSA infection or community-acquired methicillin-susceptible S. aureus (CA-MSSA) infection. Patients were interviewed 30 and 120 days after they received a diagnosis. Our primary outcome was clinical response, defined as no relapse, new S. aureus infection, or need for antibiotics at day 30.
RESULTS: Among 117 patients with skin infection, the nonresponse rate at day 30 was similar among patients with CA-MRSA infection and those with CA-MSSA infection (23 [33%] of 70 vs. 13 [28%] of 47 patients; P=.55). Lack of incision and drainage was associated with nonresponse at day 30 (P=.005), but other clinical factors, including receipt of antibiotics inactive against the infecting strain, were not. Patients with CA-MSSA infection were more likely to be rehospitalized (P=.003) and to believe subjectively that they had not been cured (P=.002) at day 30. At day 30, there was a trend for close contacts of CA-MRSA-infected patients to develop a similar infection (13% vs. 4%; odds ratio, 3.3; 95% confidence interval, 0.7-15.8; P=.2).
CONCLUSION: Although it is believed patients with CA-MRSA skin infection may have more serious outcomes than those with CA-MSSA skin infection, we found similar outcomes in these 2 groups after hospital discharge. Clinical nonresponse at day 30 was associated with a lack of receipt of incision and drainage. Our data also suggest that close contacts of persons with CA-MRSA skin infection may have a higher likelihood of acquiring an infection.

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Year:  2007        PMID: 17243049     DOI: 10.1086/511041

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  47 in total

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Review 6.  Mouse models for infectious diseases caused by Staphylococcus aureus.

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7.  Macrophages and innate immune memory against Staphylococcus skin infections.

Authors:  Jonas D Van Belleghem; Paul L Bollyky
Journal:  Proc Natl Acad Sci U S A       Date:  2018-11-02       Impact factor: 11.205

8.  Epidemiologic Similarities in Pediatric Community-Associated Methicillin-Resistant and Methicillin-Sensitive Staphylococcus aureus in the San Francisco Bay Area.

Authors:  Michelle S Hsiang; Rita Shiau; Joelle Nadle; Liana Chan; Brian Lee; Henry F Chambers; Erica Pan
Journal:  J Pediatric Infect Dis Soc       Date:  2012-07-13       Impact factor: 3.164

9.  Exploring extra-cellular proteins in methicillin susceptible and methicillin resistant Staphylococcus aureus by liquid chromatography-tandem mass spectrometry.

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10.  Rapid detection of Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) in wound specimens and blood cultures: multicenter preclinical evaluation of the Cepheid Xpert MRSA/SA skin and soft tissue and blood culture assays.

Authors:  D M Wolk; M J Struelens; P Pancholi; T Davis; P Della-Latta; D Fuller; E Picton; R Dickenson; O Denis; D Johnson; K Chapin
Journal:  J Clin Microbiol       Date:  2009-01-14       Impact factor: 5.948

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