Independent risk factors for the co-colonization of vancomycin-resistant Enterococcus faecalis and methicillin-resistant Staphylococcus aureus in the region most endemic for vancomycin-resistant Staphylococcus aureus isolation
In the majority of cases of vancomycin-resistant Staphylococcus aureus (VRSA), vancomycin-resistant Enterococcus faecalis (VR E. faecalis ) served as the vanA donor to S. aureus . Previous studies that evaluated the risk factors for co-colonization with VRE and MRSA did not differentiate between VR...
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Published in: | European journal of clinical microbiology & infectious diseases Vol. 32; no. 6; pp. 815 - 820 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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Springer-Verlag
01-06-2013
Springer Springer Nature B.V |
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Abstract | In the majority of cases of vancomycin-resistant
Staphylococcus aureus
(VRSA), vancomycin-resistant
Enterococcus faecalis
(VR
E. faecalis
) served as the
vanA
donor to
S. aureus
. Previous studies that evaluated the risk factors for co-colonization with VRE and MRSA did not differentiate between VR
E. faecalis
and VR
E. faecium
. This study aimed to identify variables associated with VR
E. faecalis
and MRSA co-colonization. A retrospective case–control study from January 2008 to December 2009 was conducted at the Detroit Medical Center. Data were extracted from charts and pharmacy records. Unique patients co-colonized with VR
E. faecalis
and MRSA (defined as isolation of MRSA within 7 days of VR
E. faecalis
isolation) were compared with patients with VR
E. faecalis
who were not co-colonized with MRSA. A total of 546 patients with VR
E. faecalis
isolation were identified. 85 (15.6 %) VR
E. faecalis
patients were co-colonized with MRSA and 461 (84.4 %) VR
E. faecalis
patients were not co-colonized with MRSA. The mean age of the study cohort was 65.9 ± 16.4 years, 424 (77.7 %) were African–American, and 270 (49.5 %) were residing in long-term care institutions. Independent predictors of co-colonization of VR
E. faecalis
and MRSA were male gender, impaired consciousness, ICU stay prior to VR
E. faecalis
isolation, indwelling devices, and isolation of VR
E. faecalis
from wounds. MRSA was frequently isolated from the same culture specimen as VR
E. faecalis
(
n
= 39, 45.9 %), most commonly from wounds. This large study of patients with VR
E. faecalis
identified the severity of illness, indwelling devices, and chronic wounds as independent predictors of co-colonization with VR
E. faecalis
and MRSA |
---|---|
AbstractList | In the majority of cases of vancomycin-resistant
Staphylococcus aureus
(VRSA), vancomycin-resistant
Enterococcus faecalis
(VR
E. faecalis
) served as the
vanA
donor to
S. aureus
. Previous studies that evaluated the risk factors for co-colonization with VRE and MRSA did not differentiate between VR
E. faecalis
and VR
E. faecium
. This study aimed to identify variables associated with VR
E. faecalis
and MRSA co-colonization. A retrospective case–control study from January 2008 to December 2009 was conducted at the Detroit Medical Center. Data were extracted from charts and pharmacy records. Unique patients co-colonized with VR
E. faecalis
and MRSA (defined as isolation of MRSA within 7 days of VR
E. faecalis
isolation) were compared with patients with VR
E. faecalis
who were not co-colonized with MRSA. A total of 546 patients with VR
E. faecalis
isolation were identified. 85 (15.6 %) VR
E. faecalis
patients were co-colonized with MRSA and 461 (84.4 %) VR
E. faecalis
patients were not co-colonized with MRSA. The mean age of the study cohort was 65.9 ± 16.4 years, 424 (77.7 %) were African–American, and 270 (49.5 %) were residing in long-term care institutions. Independent predictors of co-colonization of VR
E. faecalis
and MRSA were male gender, impaired consciousness, ICU stay prior to VR
E. faecalis
isolation, indwelling devices, and isolation of VR
E. faecalis
from wounds. MRSA was frequently isolated from the same culture specimen as VR
E. faecalis
(
n
= 39, 45.9 %), most commonly from wounds. This large study of patients with VR
E. faecalis
identified the severity of illness, indwelling devices, and chronic wounds as independent predictors of co-colonization with VR
E. faecalis
and MRSA In the majority of cases of vancomycin-resistant Staphylococcus aureus (VRSA), vancomycin-resistant Enterococcus faecalis (VR E. faecalis) served as the vanA donor to S. aureus. Previous studies that evaluated the risk factors for co-colonization with VRE and MRSA did not differentiate between VR E. faecalis and VR E. faecium. This study aimed to identify variables associated with VR E. faecalis and MRSA co-colonization. A retrospective case-control study from January 2008 to December 2009 was conducted at the Detroit Medical Center. Data were extracted from charts and pharmacy records. Unique patients co-colonized with VR E. faecalis and MRSA (defined as isolation of MRSA within 7 days of VR E. faecalis isolation) were compared with patients with VR E. faecalis who were not co-colonized with MRSA. A total of 546 patients with VR E. faecalis isolation were identified. 85 (15.6 %) VR E. faecalis patients were co-colonized with MRSA and 461 (84.4 %) VR E. faecalis patients were not co-colonized with MRSA. The mean age of the study cohort was 65.9±16.4 years, 424 (77.7 %) were African-American, and 270 (49.5 %) were residing in long-term care institutions. Independent predictors of co-colonization of VR E. faecalis and MRSA were male gender, impaired consciousness, ICU stay prior to VR E. faecalis isolation, indwelling devices, and isolation of VR E. faecalis from wounds. MRSA was frequently isolated from the same culture specimen as VR E. faecalis (n=39, 45.9 %), most commonly from wounds. This large study of patients with VR E. faecalis identified the severity of illness, indwelling devices, and chronic wounds as independent predictors of co-colonization with VR E. faecalis and MRSA[PUBLICATION ABSTRACT] In the majority of cases of vancomycin-resistant Staphylococcus aureus (VRSA), vancomycin-resistant Enterococcus faecalis (VR E. faecalis) served as the vanA donor to S. aureus. Previous studies that evaluated the risk factors for co-colonization with VRE and MRSA did not differentiate between VR E. faecalis and VR E. faecium. This study aimed to identify variables associated with VR E. faecalis and MRSA co-colonization. A retrospective case-control study from January 2008 to December 2009 was conducted at the Detroit Medical Center. Data were extracted from charts and pharmacy records. Unique patients co-colonized with VR E. faecalis and MRSA (defined as isolation of MRSA within 7 days of VR E. faecalis isolation) were compared with patients with VR E. faecalis who were not co-colonized with MRSA. A total of 546 patients with VR E. faecalis isolation were identified. 85 (15.6 %) VR E. faecalis patients were co-colonized with MRSA and 461 (84.4 %) VR E. faecalis patients were not co-colonized with MRSA. The mean age of the study cohort was 65.9 ± 16.4 years, 424 (77.7 %) were African-American, and 270 (49.5 %) were residing in long-term care institutions. Independent predictors of co-colonization of VR E. faecalis and MRSA were male gender, impaired consciousness, ICU stay prior to VR E. faecalis isolation, indwelling devices, and isolation of VR E. faecalis from wounds. MRSA was frequently isolated from the same culture specimen as VR E. faecalis (n = 39, 45.9 %), most commonly from wounds. This large study of patients with VR E. faecalis identified the severity of illness, indwelling devices, and chronic wounds as independent predictors of co-colonization with VR E. faecalis and MRSA. In the majority of cases of vancomycin-resistant Staphylococcus aureus (VRSA), vancomycin-resistant Enterococcus faecalis (VR E. faecalis) served as the vanA donor to S. aureus. Previous studies that evaluated the risk factors for co-colonization with VRE and MRSA did not differentiate between VR E. faecalis and VR E. faecium. This study aimed to identify variables associated with VR E. faecalis and MRSA co-colonization. A retrospective case-control study from January 2008 to December 2009 was conducted at the Detroit Medical Center. Data were extracted from charts and pharmacy records. Unique patients co-colonized with VR E. faecalis and MRSA (defined as isolation of MRSA within 7 days of VR E. faecalis isolation) were compared with patients with VR E. faecalis who were not co-colonized with MRSA. A total of 546 patients with VR E. faecalis isolation were identified. 85 (15.6 %) VR E. faecalis patients were co-colonized with MRSA and 461 (84.4 %) VR E. faecalis patients were not co-colonized with MRSA. The mean age of the study cohort was 65.9 plus or minus 16.4 years, 424 (77.7 %) were African-American, and 270 (49.5 %) were residing in long-term care institutions. Independent predictors of co-colonization of VR E. faecalis and MRSA were male gender, impaired consciousness, ICU stay prior to VR E. faecalis isolation, indwelling devices, and isolation of VR E. faecalis from wounds. MRSA was frequently isolated from the same culture specimen as VR E. faecalis (n=39, 45.9 %), most commonly from wounds. This large study of patients with VR E. faecalis identified the severity of illness, indwelling devices, and chronic wounds as independent predictors of co-colonization with VR E. faecalis and MRSA |
Author | Hayakawa, K. Rybak, M. J. Khan, A. Kaye, K. S. Mustapha, M. Ajamoughli, M. Jagadeesh, K. K. Levine, M. Bathina, P. Patel, D. Moshos, J. A. Ahmed, F. Kamatam, S. Ho, K. Marchaim, D. Reddy, S. M. L. Martin, E. T. Lee, K. P. Pogue, J. M. Sunkara, B. Omotola, A. M. Suhrawardy, U. Willis, L. B. |
Author_xml | – sequence: 1 givenname: K. surname: Hayakawa fullname: Hayakawa, K. email: kayokohayakawa@gmail.com organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University, Division of Infectious Diseases, 5 Hudson – sequence: 2 givenname: D. surname: Marchaim fullname: Marchaim, D. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 3 givenname: P. surname: Bathina fullname: Bathina, P. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 4 givenname: E. T. surname: Martin fullname: Martin, E. T. organization: Department of Pharmacy Practice, Wayne State University – sequence: 5 givenname: J. M. surname: Pogue fullname: Pogue, J. M. organization: Department of Pharmacy Services, Detroit Medical Center – sequence: 6 givenname: B. surname: Sunkara fullname: Sunkara, B. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 7 givenname: S. surname: Kamatam fullname: Kamatam, S. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 8 givenname: K. surname: Ho fullname: Ho, K. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 9 givenname: L. B. surname: Willis fullname: Willis, L. B. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 10 givenname: M. surname: Ajamoughli fullname: Ajamoughli, M. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 11 givenname: D. surname: Patel fullname: Patel, D. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 12 givenname: A. surname: Khan fullname: Khan, A. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 13 givenname: K. P. surname: Lee fullname: Lee, K. P. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 14 givenname: U. surname: Suhrawardy fullname: Suhrawardy, U. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 15 givenname: K. K. surname: Jagadeesh fullname: Jagadeesh, K. K. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 16 givenname: S. M. L. surname: Reddy fullname: Reddy, S. M. L. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 17 givenname: M. surname: Levine fullname: Levine, M. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 18 givenname: F. surname: Ahmed fullname: Ahmed, F. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 19 givenname: A. M. surname: Omotola fullname: Omotola, A. M. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 20 givenname: M. surname: Mustapha fullname: Mustapha, M. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 21 givenname: J. A. surname: Moshos fullname: Moshos, J. A. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University – sequence: 22 givenname: M. J. surname: Rybak fullname: Rybak, M. J. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University, Anti-Infective Research Laboratory, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University – sequence: 23 givenname: K. S. surname: Kaye fullname: Kaye, K. S. organization: Division of Infectious Diseases, Detroit Medical Center, Wayne State University |
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CitedBy_id | crossref_primary_10_3390_antibiotics11010049 crossref_primary_10_1186_s12941_019_0327_8 crossref_primary_10_3390_ph16040564 crossref_primary_10_1128_AAC_01507_18 crossref_primary_10_1016_j_ajic_2018_09_026 crossref_primary_10_1016_j_idc_2016_05_001 crossref_primary_10_1017_ice_2022_57 crossref_primary_10_1016_j_envint_2020_105914 crossref_primary_10_1016_j_idc_2021_04_013 crossref_primary_10_3389_fmicb_2019_02453 crossref_primary_10_1073_pnas_1718712115 crossref_primary_10_1016_j_ajic_2019_11_010 crossref_primary_10_1007_s10096_015_2436_4 crossref_primary_10_1016_j_jare_2019_10_005 |
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Keywords | Functional Status Deterioration Surveillance Culture Chronic Skin Ulcer Impaired Consciousness vanA Gene Enterococcus faecalis Microbiology Infection Streptococcaceae Risk factor Bacteriosis Bacteria Micrococcales Isolation Micrococcaceae Staphylococcal infection Colonization Staphylococcus aureus |
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Staphylococcus aureus
(VRSA), vancomycin-resistant
Enterococcus faecalis
(VR
E. faecalis
) served as the
vanA... In the majority of cases of vancomycin-resistant Staphylococcus aureus (VRSA), vancomycin-resistant Enterococcus faecalis (VR E. faecalis) served as the vanA... |
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SubjectTerms | Activities of daily living Aged Aged, 80 and over Antibiotic resistance Bacterial diseases Biological and medical sciences Biomedical and Life Sciences Biomedicine Case-Control Studies Coinfection Colonization Drug Resistance, Bacterial Enterococcus faecalis Enterococcus faecalis - drug effects Enterococcus faecalis - isolation & purification Female Gram-Positive Bacterial Infections - epidemiology Hospitals Human bacterial diseases Humans Infectious diseases Internal Medicine Long-term care Male Medical Microbiology Medical sciences Methicillin-Resistant Staphylococcus aureus - drug effects Methicillin-Resistant Staphylococcus aureus - isolation & purification Middle Aged Mortality Odds Ratio Patients Pharmacy Retrospective Studies Risk Factors Staphylococcal Infections - epidemiology Staphylococcal infections, streptococcal infections, pneumococcal infections Staphylococcus aureus Staphylococcus infections Vancomycin - pharmacology |
Title | Independent risk factors for the co-colonization of vancomycin-resistant Enterococcus faecalis and methicillin-resistant Staphylococcus aureus in the region most endemic for vancomycin-resistant Staphylococcus aureus isolation |
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