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现行 KS P ISO 16256-2017
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임상검사실 검사 및 체외진단용 의료기기 ─ 감염성 진균감염에서의 항진균제 감수성 검사의 참조(기준)방법 临床实验室检测和体外诊断检测系统─检测抗菌药物对感染酵母菌的体外活性的参考方法
发布日期: 2017-12-29
该标准规定了对包括引起感染的坎迪多种(Candida spp.)及Cryptoccus neoformans在内的酵母抗真菌药的易感性方法。这里说明的标准方法从未用于两种形式的霉菌研究,如粉芽菌症(B.dermatitidis)和/或希氏锥虫症(H.capsulatum)变种胶囊锂(capsulatum)。另外,丝状真菌(菌丝型)试验还显示了在目前程序中标准化中没有提及的一些附加问题。作为抗真菌敏感性试验法,推荐的液体培养基稀释法不断发展,现在可以使用CLSI文档M38及EUCAST文档E.DEF9.1[4][5][6][7][8]等。
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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