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伤口拭子质量分级取决于革兰氏染色筛查方法。

Wound swab quality grading is dependent on Gram smear screening approach.

机构信息

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.

Eastern Ontario Regional Laboratory Association, Ottawa, Canada.

出版信息

Sci Rep. 2023 Feb 23;13(1):3160. doi: 10.1038/s41598-023-29832-1.

Abstract

Superficial skin swab collections are inherently low-quality and may be of little clinical value due to their poor sensitivity and specificity. Clinical microbiology laboratories can use Gram smears to screen and differentiate higher and lower quality specimens to direct the extent of potential pathogen work up, including antimicrobial susceptibility testing (AST). We compared the impact of two different smear grading approaches to our current reporting practices for superficial wound swab cultures. Two variations of the Q score methodology (low power under 10X (QS10) and high power under 100X (QS100) were compared to our existing oil immersion method (OM100) (100X). We further evaluated the QS100 method by scoring superficial swab smears previously screened by OM100 from cultures submitted between November 2018 and December 2019. No significant difference in the number of low-quality specimens (N = 50) was identified by QS10 or QS100 grading (N = 9; 18%; N = 8; 16% respectively). Among 968 additional QS100 screened smears, 67 (6.9%) low quality swabs were identified and 7.4% fewer organisms (76/1020 organisms) would require reporting with AST. Implementing the Q score for superficial wound swab cultures would provide minimal improvements in their clinical relevance, laboratory quality and efficiency in our laboratory due to the low number of poor-quality swabs received.

摘要

表面皮肤拭子采集本身质量较差,由于其敏感性和特异性差,可能临床价值有限。临床微生物学实验室可以使用革兰氏染色来筛选和区分高质量和低质量的标本,以指导潜在病原体检测的程度,包括抗菌药物敏感性测试(AST)。我们比较了两种不同的涂片分级方法对我们目前表面伤口拭子培养报告实践的影响。两种 Q 评分方法(低倍镜下 10 倍(QS10)和高倍镜下 100 倍(QS100))与我们现有的油浸法(OM100)(100 倍)进行了比较。我们进一步评估了 QS100 方法,对 OM100 筛选的表面拭子涂片进行评分,这些标本来自 2018 年 11 月至 2019 年 12 月提交的培养物。通过 QS10 或 QS100 分级(N = 9;18%;N = 8;16%),低质量标本的数量(N = 50)没有显著差异。在另外 968 个 QS100 筛选的拭子中,有 67 个(6.9%)低质量拭子被识别,需要进行 AST 的微生物数量减少了 7.4%(76/1020 个微生物)。在我们的实验室中,由于收到的低质量拭子数量较少,实施 Q 评分对浅表性伤口拭子培养物的临床相关性、实验室质量和效率的改善作用很小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3592/9950449/361b204c3fc4/41598_2023_29832_Fig1_HTML.jpg

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