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首页> 外文期刊>American Journal of Tropical Medicine and Hygiene >Increasing Fluoroquinolone Resistance in Salmonella typhi in Ontario, 2002-2007
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Increasing Fluoroquinolone Resistance in Salmonella typhi in Ontario, 2002-2007

机译:2002-2007年安大略省伤寒沙门氏菌对氟喹诺酮类药物的耐药性增加

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摘要

We reviewed the antibiotic susceptibility patterns of all isolates of Salmonella typhi in Ontario, Canada from January 2002 to December 2007. We identified a total of 381 unique cases over the 5-year period (50–73 cases per year). Of the 381 cases, 171 were female, 164 were male, and no gender was identified for 33 cases. Age of the patients ranged from less than 1 to 102 years of age (median age of 20 years). Although resistance patterns for ampicillin, trimethoprim-sulfamethoxazole, third generation cephalosporins (cefotaxime until May 2005 and ceftriaxone from June 2005 to present), and chloramphenicol remained stable, nalidixic acid resistance rose sharply between 2003 and 2005 and has remained at approximately 80% of isolates since 2005. The significant and sustained increase in nalidixic acid-resistant S. typhi suggests that ciprofloxacin should no longer be used as the drug of choice for the empiric treatment of typhoid fever in Ontario.
机译:我们回顾了2002年1月至2007年12月在加拿大安大略省伤寒沙门氏菌的所有分离株的抗生素敏感性模式。我们确定了在 < / sup> 5年期(每年50-73例)。在381例病例中, 为女性,164例为男性,33例中未发现性别。患者的年龄范围从小于1到 102岁(中位年龄为20岁)。尽管氨苄西林,甲氧苄氨嘧啶,磺胺甲恶唑,第三代头孢菌素(头孢噻肟至2005年5月和头孢曲松酮 从2005年6月至今)和氯霉素的耐药性 模式自2003年至2005年, 对亚硝酸的耐药性急剧上升,自2005年以来一直保持在约80%的分离株中。 显着且持续的增长在耐萘啶酸的 S中。伤寒建议不再使用环丙沙星 作为安大略省典型治疗伤寒的药物。

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  • 来源
    《American Journal of Tropical Medicine and Hygiene 》 |2009年第6期| 1012-1013| 共2页
  • 作者单位

    Division of Infectious Diseases, Hospital for Sick Childrenand The University of Toronto, Toronto, Canada;

    Department ofMicrobiology, Hospital for Sick Children, The University ofToronto, and Ontario Agency for Health Protection and Promotion,Toronto, Canada;

    Division of Infectious and Immunologic Diseases,British Columbia Children’s Hospital and The Universityof British Columbia, Vancouver, Canada;

    Division of Social Pediatrics,Hospital of Sick Children and The University of Toronto, Toronto,Canada;

    Department of Laboratory Medicine and Pathobiology,The University of Toronto and Ontario Agency for Health Protectionand Promotion, Toronto, Canada;

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