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现行 KS P ISO 16256-2022
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임상검사 실 검사 및 체외진단 검사 시스템 감염성 효모 형 진 균에 대한 항균제 액체배지 미량희석 감수성 검사의 참조 참조(기준기준)방법 临床实验室试验和体外诊断试验系统.检测抗微生物剂对感染性疾病中酵母真菌体外活性的肉汤微稀释参考法
发布日期: 2022-12-28
该标准规定了酵母菌抗真菌药物的感受性方法,包括引起感染的坎迪达种(Candida spp.)和Cryptococcus neoformans。这里介绍的标准方法从未用于研究两种形态的霉菌,如分枝杆菌症(B.dermatitidis)和/或肉芽肿症(H.capsulatum)变种胶囊锂(capsulatum)。此外,思想型真菌(菌丝型)试验还显示了目前程序中未在标准化中提及的几个额外问题。作为抗真菌感受性试验法推荐的液体培养基稀释法不断发展,现在CLSI文档M38和EUCAST文档E.DEF9.1[4][5][6][7][8]等可用。
이 표준은 감염을 일으키는 칸디다 종(Candida spp.) 및 크립토코쿠스증 (Cryptococcus neoformans) 를 포함하는 효모 항진균제에 대한 감수성 방법을 규정한다. 여기에서 설명한 기준 방법은 분아균증 (B. dermatitidis) 및/또는 히스토플라즈마증(H.capsulatum) 변종 캡슐라튬(capsulatum)과 같은 두형태의 곰팡이 연구에 사용된 적은 없다. 또한 사상형진균(균사형) 시험은 현재 절차에서는 표준화에서 언급되지 않았던 몇 가지 추가 문제점을 보여준다. 항진균 감수성 시험법으로서 추천되는 액체배지 희석법은 계속 발전하였으며, 지금은 CLSI 문서 M38 및 EUCAST 문서 E.DEF 9.1 [4][5][6][7][8] 등이 사용 가능 하다.
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发布单位或类别: 韩国-韩国标准
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