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Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents

Background. Methicillin-resistant Staphylococcus aureus (MRSA) infection incidence has increased in healthy US children. Our objective was to evaluate MRSA incidence and correlates in HIV-infected youth. Methods. The CDC-sponsored LEGACY study is a US multicenter chart abstraction study of HIV-infec...

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Autores principales: Siberry, George K., Frederick, Toni, Emmanuel, Patricia, Paul, Mary E., Bohannon, Beverly, Wheeling, Travis, Barton, Theresa, Rathore, Mobeen H., Dominguez, Kenneth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447349/
https://www.ncbi.nlm.nih.gov/pubmed/23008761
http://dx.doi.org/10.1155/2012/627974
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author Siberry, George K.
Frederick, Toni
Emmanuel, Patricia
Paul, Mary E.
Bohannon, Beverly
Wheeling, Travis
Barton, Theresa
Rathore, Mobeen H.
Dominguez, Kenneth L.
author_facet Siberry, George K.
Frederick, Toni
Emmanuel, Patricia
Paul, Mary E.
Bohannon, Beverly
Wheeling, Travis
Barton, Theresa
Rathore, Mobeen H.
Dominguez, Kenneth L.
author_sort Siberry, George K.
collection PubMed
description Background. Methicillin-resistant Staphylococcus aureus (MRSA) infection incidence has increased in healthy US children. Our objective was to evaluate MRSA incidence and correlates in HIV-infected youth. Methods. The CDC-sponsored LEGACY study is a US multicenter chart abstraction study of HIV-infected youth. We identified MRSA infections among participants with ≥1 visit during 2006. We used bivariate and multivariable analyses to compare sociodemographic and HIV clinical factors between MRSA cases and noncases. Results. Fourteen MRSA infections (1 invasive, 12 soft tissue, 1 indeterminate) occurred among 1,813 subjects (11.1 infections/1,000 patient-years (PY), 95% CI: 11.06–11.14). Most (86%) isolates were clindamycin susceptible. Compared with noncases, MRSA cases were more likely older (17 versus 14 years), black (100% versus 69%), behaviorally HIV infected (43% versus 17%), and in Maryland (43% versus 7%) and had viral loads (VL) >1000 copies/mL (86% versus 51%) and lower mean CD4% (18% versus 27%) (all P < 0.05). In multivariate analysis, independent risk factors were Maryland care site (adjusted odds ratio (aOR) = 9.0), VL >1000 copies/mL (aOR = 5.9), and black race (aOR undefined). Conclusions. MRSA occurred at a rate of 11.1 infections/1,000 PY in HIV-infected youth but invasive disease was uncommon. Geographic location, black race, and increased VL, but not immunosuppression, were independently associated with MRSA risk.
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spelling pubmed-34473492012-09-24 Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents Siberry, George K. Frederick, Toni Emmanuel, Patricia Paul, Mary E. Bohannon, Beverly Wheeling, Travis Barton, Theresa Rathore, Mobeen H. Dominguez, Kenneth L. AIDS Res Treat Research Article Background. Methicillin-resistant Staphylococcus aureus (MRSA) infection incidence has increased in healthy US children. Our objective was to evaluate MRSA incidence and correlates in HIV-infected youth. Methods. The CDC-sponsored LEGACY study is a US multicenter chart abstraction study of HIV-infected youth. We identified MRSA infections among participants with ≥1 visit during 2006. We used bivariate and multivariable analyses to compare sociodemographic and HIV clinical factors between MRSA cases and noncases. Results. Fourteen MRSA infections (1 invasive, 12 soft tissue, 1 indeterminate) occurred among 1,813 subjects (11.1 infections/1,000 patient-years (PY), 95% CI: 11.06–11.14). Most (86%) isolates were clindamycin susceptible. Compared with noncases, MRSA cases were more likely older (17 versus 14 years), black (100% versus 69%), behaviorally HIV infected (43% versus 17%), and in Maryland (43% versus 7%) and had viral loads (VL) >1000 copies/mL (86% versus 51%) and lower mean CD4% (18% versus 27%) (all P < 0.05). In multivariate analysis, independent risk factors were Maryland care site (adjusted odds ratio (aOR) = 9.0), VL >1000 copies/mL (aOR = 5.9), and black race (aOR undefined). Conclusions. MRSA occurred at a rate of 11.1 infections/1,000 PY in HIV-infected youth but invasive disease was uncommon. Geographic location, black race, and increased VL, but not immunosuppression, were independently associated with MRSA risk. Hindawi Publishing Corporation 2012 2012-09-12 /pmc/articles/PMC3447349/ /pubmed/23008761 http://dx.doi.org/10.1155/2012/627974 Text en Copyright © 2012 George K. Siberry et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Siberry, George K.
Frederick, Toni
Emmanuel, Patricia
Paul, Mary E.
Bohannon, Beverly
Wheeling, Travis
Barton, Theresa
Rathore, Mobeen H.
Dominguez, Kenneth L.
Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents
title Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents
title_full Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents
title_fullStr Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents
title_full_unstemmed Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents
title_short Methicillin-Resistant Staphylococcus aureus Infections in Human Immunodeficiency Virus-Infected Children and Adolescents
title_sort methicillin-resistant staphylococcus aureus infections in human immunodeficiency virus-infected children and adolescents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447349/
https://www.ncbi.nlm.nih.gov/pubmed/23008761
http://dx.doi.org/10.1155/2012/627974
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