Evaluation of a cefoxitin 30 microg disc on Iso-Sensitest agar for detection of methicillin-resistant Staphylococcus aureus.

Evaluation of a cefoxitin 30 microg disc on Iso-Sensitest agar for detection of methicillin-resistant Staphylococcus aureus.
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对 Iso-Sensitest 琼脂上的头孢西丁 30 微克圆片用于检测耐甲氧西林金黄色葡萄球菌的评估。

DOI:
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发表时间:
2003
影响因子:
5.2
通讯作者:
G. Kahlmeter
G. Kahlmeter
中科院分区:
医学2区
文献类型:
--
作者:
R. Skov;R. Smyth;M. Clausen;A. Larsen;N. Frimodt;B. Olsson;G. Kahlmeter

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目标 为了评估头孢西丁 30 微克圆片在 Iso-Sensitest 琼脂上的性能,使用半汇合接种物并在 35-36°C 下孵育过夜,用于检测耐甲氧西林金黄色葡萄球菌 (MRSA)。 方法 使用半汇合接种物并在 35-36 摄氏度下过夜孵育,用头孢西丁 30 微克圆盘在 Iso-Sensitest 琼脂上测试了总共 457 株金黄色葡萄球菌,包括几种定义的 PFGE 类型的 190 株 MRSA 和一些低水平耐药菌株。该方法与标准 SRGA(瑞典抗生素参考组)方法进行了比较 (苯唑西林 1 微克圆片置于补充有 5% 去纤维马血的 Iso-Sensitest 琼脂上,汇合生长并在 30 摄氏度环境空气中孵育 24 小时)。 结果 头孢西丁方法非常出色,使用 S > 或 = 29 mm 且 R < 29 mm 的解释区直径,灵敏度为 100%,特异性为 99%。它的性能比 SRGA 方法好得多,SRGA 方法在使用当前 S > 或 = 12 mm 的断点时,对于困难菌株的集合,其灵敏度仅为 78%。 结论 我们建议头孢西丁方法应取代 SRGA 目前推荐的 MRSA 检测方法,并且该方法非常适合 BSAC 方法。
OBJECTIVES To evaluate the performance of a cefoxitin 30 microg disc on Iso-Sensitest agar, using a semi-confluent inoculum and overnight incubation at 35-36 degrees C, for detection of methicillin-resistant Staphylococcus aureus (MRSA). METHODS A total of 457 S. aureus, including 190 MRSA of several defined PFGE types and a number of low-level resistant isolates, were tested with a cefoxitin 30 microg disc on Iso-Sensitest agar, using a semi-confluent inoculum and overnight incubation at 35-36 degrees C. This method was compared with the standard SRGA (Swedish Reference Group for Antibiotics) method (oxacillin 1 microg disc on Iso-Sensitest agar supplemented with 5% defibrinated horse blood, confluent growth and 24 h incubation in ambient air at 30 degrees C). RESULTS The cefoxitin method was excellent, with a sensitivity of 100% and a specificity of 99% using an interpretative zone diameter of S > or = 29 mm and R < 29 mm. Its performance was much better than the SRGA method, which with this collection of difficult strains had a sensitivity of only 78% using the current breakpoint of S > or = 12 mm. CONCLUSION We suggest that the cefoxitin method should replace that currently recommended by the SRGA for the detection of MRSA, and that it would fit well into BSAC methodology.