Methicillin-ResistantStaphylococcus aureusInfections in Human Immunodeficiency Virus-Infected Children and Adolescents
Author(s) -
George K. Siberry,
Toni Frederick,
Patricia Emmanuel,
Mary E. Paul,
Beverly Bohan,
Travis Wheeling,
Theresa Barton,
Mobeen H. Rathore,
Kenneth L. Dominguez
Publication year - 2012
Publication title -
aids research and treatment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.749
H-Index - 27
eISSN - 2090-1259
pISSN - 2090-1240
DOI - 10.1155/2012/627974
Subject(s) - staphylococcus aureus , medicine , human immunodeficiency virus (hiv) , virology , microbiology and biotechnology , biology , bacteria , genetics
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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