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The International Circumpolar Surveillance Interlaboratory Quality Control Program for Streptococcus pneumoniae, 1999 to 2008▿

机译:1999年至2008年国际肺炎链球菌实验室间质控间质量控制计划

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摘要

The International Circumpolar Surveillance (ICS) Program was initiated in 1999 to conduct population-based surveillance for invasive pneumococcal disease in select regions of the Arctic. An interlaboratory quality control (QC) program for pneumococcal serotyping and antibiotic susceptibility testing was incorporated into ICS by reference laboratories in northern Canada (Laboratoire de Santé Publique du Québec [LSPQ] in Sainte-Anne de Bellevue, Québec; National Centre for Streptococcus [NCS] in Edmonton, Alberta) and Alaska (Arctic Investigations Program [AIP]). The World Health Organization's Collaborating Centre for Reference and Research on Pneumococci at the Statens Serum Institute (SSI) in Copenhagen, Denmark, joined the QC program in 2004. The Iceland Reference Laboratory (IRL) in Reykjavik, Iceland, joined the QC program in 2006, but due to small sample sizes, data from IRL are not included in this report. From 1999 through 2008, 190 isolates were distributed among four laboratories (AIP, NCS, LSPQ, and SSI). The overall serotype concordance was 95.8%, and the overall serogroup concordance was 97.4%. The overall modal MIC concordance for testing by broth microdilution (BMD) and agar dilution was >96% for all the antibiotics except erythromycin (92.1%) and clindamycin (89.5%). MIC comparisons between the Etest and BMD resulted in lower concordance for erythromycin (73.9%), clindamycin (65.5%), and trimethoprim-sulfamethoxazole (80%); however, categorical concordance (susceptible, resistant) remained high at 98.6%, 89.1%, and 90.9%, respectively. Our data demonstrate a high degree of correlation of serotyping and antimicrobial susceptibility testing results between four participating laboratories.
机译:国际环极监视(ICS)计划于1999年启动,目的是对北极某些地区的侵袭性肺炎球菌疾病进行基于人群的监视。加拿大北部的参考实验室(魁北克省Sainte-Anne de Bellevue的Laboratoire deSantéPublique duQuébec[LSPQ];国家链球菌中心[NCS])将用于肺炎球菌血清分型和抗生素敏感性测试的实验室间质量控制(QC)计划纳入了ICS。 ](艾伯塔省埃德蒙顿)和阿拉斯加(北极调查计划[AIP])。丹麦哥本哈根史坦顿血清研究所(SSI)的世界卫生组织肺炎球菌参考和研究合作中心于2004年加入质量控制计划。冰岛雷克雅未克的冰岛参考实验室(IRL)于2006年加入了质量控制计划。 ,但由于样本量较小,IRL的数据未包含在此报告中。从1999年到2008年,在四个实验室(AIP,NCS,LSPQ和SSI)之间分配了190个分离株。总体血清型一致性为95.8%,总体血清型一致性为97.4%。除红霉素(92.1%)和克林霉素(89.5%)外,所有抗生素通过肉汤微稀释液(BMD)和琼脂稀释测试的总体模态MIC一致性均> 96%。 Etest和BMD之间的MIC比较发现,红霉素(73.9%),克林霉素(65.5%)和甲氧苄氨嘧啶-磺胺甲恶唑(80%)的一致性较低。但是,类别一致性(易感性,抗性)仍然很高,分别为98.6%,89.1%和90.9%。我们的数据表明四个参与实验室之间的血清分型和抗菌药敏试验结果高度相关。

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