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Please note that all translations are automatically generated. Click here for the English version.
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02:18 min
May 24th, 2024
DOI :
10.3791/66588-v
Transcript
本研究旨在通过自动微生物鉴定系统直接从阳性标记血培养瓶中评估革兰氏阴性菌的诊断准确性。目的是将其用作 EUCAST 快速药敏试验方法早期临床报告的工具。EUCAST RAST 方法最近于 2018 年推出,可在自动血培养瓶出现阳性标记后的 4 至 8 小时内报告抗微生物药敏测试结果。
它涉及直接从带有正向标记的瓶子中执行无处不在的圆盘扩散方法,并在 4 小时、6 小时或 8 小时内读取结果。对于通过 EUCAST RAST 方法进行的临床报告,微生物鉴定是确定 AST 结果解释
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