Identification methods as a factor affecting the performance of clinical microbiology laboratories participating in an external quality assessment program: a cross-sectional, retrospective analysis.

Jennifer Wu, Md Saiful Alam, Veronica Restelli, Selvarani Vimalanathan, Lucy A Perrone
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Abstract

Introduction. Laboratory participation in external quality assessment (EQA) programmes including proficiency testing (PT) is a requirement of clinical laboratory conformance to ISO 15189:2022 Medical laboratories - Requirements for quality and competence. PT is one EQA method whereby laboratories are sent blinded samples for characterization by routine laboratory diagnostic methods. Importantly, PT enables a laboratory's performance to be evaluated in comparison to the standard reference methods and to the performance of other peer laboratories using similar diagnostic methods.Gap statement. The desired outcome of participating in PT is to help laboratories identify possible sources of error in each step of the total testing process and particularly in their test methods during the analytical phase.Aim. This cross-sectional study investigated the impact of using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) compared to conventional phenotypic biochemical testing on laboratory performance in a clinical bacteriology PT scheme.Methodology. During a 6-year period from 2017-2022, the Canadian Microbiology Proficiency Testing implemented 112 PT challenges comprising 22 different sample types and included 61 different bacterial species. This was translated into 5883 graded test events for analysis. Multiple logistic regression techniques were employed to explore the association between the test method employed and laboratory performance. The sample type and aerobic classification of challenge organisms were included as confounding variables.Results. Laboratories using MALDI-TOF MS performed significantly better in characterizing microorganisms than laboratories using phenotypic biochemical testing alone [odds ratio OR = 5.68, confidence interval (CI): 3.92, 8.22] regardless of the sample type and aerobic classification. Notably, our analysis identified a significant association between anaerobic organisms and laboratory performance (OR: 0.24, CI: 0.17-0.35), suggesting that culturing and identifying fastidious organisms remains a significant obstacle for many clinical microbiology laboratories.Conclusions. Although no method is infallible and its performance will depend on the validation and quality assurance procedures, this finding may help the management in the decision for implementing MALDI-TOF MS in the microbiology laboratory. This study highlights the important role PT providers play in the objective assessment of laboratory performance and how it can provide evidence for quality improvement.

鉴定方法是影响参与外部质量评估计划的临床微生物实验室绩效的一个因素:一项横断面回顾性分析。
导言。实验室参与外部质量评估(EQA)计划,包括能力验证(PT),是临床实验室符合 ISO 15189:2022 《医学实验室--质量和能力要求》的一项要求。能力考查是一种 EQA 方法,通过这种方法,实验室会被送去盲样,用常规实验室诊断方法进行鉴定。重要的是,通过与标准参考方法和使用类似诊断方法的其他同行实验室进行比较,PT 可以对实验室的绩效进行评估。参与 PT 的预期结果是帮助实验室识别整个检测过程中每个步骤可能存在的误差来源,尤其是分析阶段的检测方法。这项横断面研究调查了在临床细菌学PT计划中,使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)与传统的表型生化检测相比,对实验室绩效的影响。在2017-2022年的6年时间里,加拿大微生物能力验证实施了112项PT挑战,包括22种不同的样本类型和61种不同的细菌种类。这转化为 5883 个分级测试事件供分析。我们采用了多元逻辑回归技术来探讨所采用的检测方法与实验室绩效之间的关联。样本类型和挑战微生物的需氧分类被列为混杂变量。无论样品类型和需氧分类如何,使用 MALDI-TOF MS 的实验室在鉴定微生物特性方面的表现明显优于仅使用表型生化检测的实验室[几率比 OR = 5.68,置信区间 (CI):3.92, 8.22]。值得注意的是,我们的分析发现厌氧菌与实验室绩效之间存在显著关联(OR:0.24,CI:0.17-0.35),这表明培养和鉴定需氧菌仍是许多临床微生物实验室的一大障碍。尽管没有一种方法是无懈可击的,其性能也取决于验证和质量保证程序,但这一发现可能有助于管理层决定是否在微生物实验室实施 MALDI-TOF MS。这项研究强调了PT提供者在客观评估实验室绩效方面的重要作用,以及如何为质量改进提供证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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