4 research outputs found

    Incidence of Cronobacter spp. Infections, United States, 2003ā€“2009

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    During 2003ā€“2009, we identified 544 cases of Cronobacter spp. infection from 6 US states. The highest percentage of invasive infections occurred among children <5 years of age; urine isolates predominated among adults. Rates of invasive infections among infants approximate earlier estimates. Overall incidence of 0.66 cases/100,000 population was higher than anticipated

    Risk of Hemolytic Uremic Syndrome Related to Treatment of Escherichia coli O157 Infection with Different Antimicrobial Classes

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    Treatment of Shiga toxin-producing Escherichia coli O157 (O157) diarrhea with antimicrobials might alter the risk of hemolytic uremic syndrome (HUS). However, full characterization of which antimicrobials might affect risk is lacking, particularly among adults. To inform clinical management, we conducted a case-control study of residents of the FoodNet surveillance areas with O157 diarrhea during a 4-year period to assess antimicrobial class-specific associations with HUS among persons with O157 diarrhea. We collected data from medical records and patient interviews. We measured associations between treatment with agents in specific antimicrobial classes during the first week of diarrhea and development of HUS, adjusting for age and illness severity. We enrolled 1308 patients; 102 (7.8%) developed confirmed HUS. Antimicrobial treatment varied by age: &lt;5 years (12.6%), 5ā€“14 (11.5%), 15ā€“39 (45.4%), ā‰„40 (53.4%). Persons treated with a Ī²-lactam had higher odds of developing HUS (OR 2.80, CI 1.14ā€“6.89). None of the few persons treated with a macrolide developed HUS, but the protective association was not statistically significant. Exposure to ā€œany antimicrobialā€ was not associated with increased odds of HUS. Our findings confirm the risk of Ī²-lactams among children with O157 diarrhea and extends it to adults. We observed a high frequency of inappropriate antimicrobial treatment among adults. Our data suggest that antimicrobial classes differ in the magnitude of risk for persons with O157 diarrhea
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