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2019年冠状病毒病大流行期间常规诊断实验室的生物安全风险评估

Biosafety Risk Assessment of a Routine Diagnostic Laboratory During the Coronavirus Disease 2019 Pandemic.

作者信息

Zorbozan Orçun, Zorbozan Nergiz, Turgay Nevin

机构信息

Department of Parasitology, Ege University Faculty of Medicine, İzmir, Turkey.

Department of Biochemistry, Kemalpaşa State Hospital, İzmir, Turkey.

出版信息

Appl Biosaf. 2021 Sep;26(Suppl 1):S2-S9. doi: 10.1089/apb.20.0064. Epub 2021 Sep 13.

DOI:10.1089/apb.20.0064
PMID:36032648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9135154/
Abstract

In this study, we aimed to perform a biosafety risk assessment to determine measures to be taken against coronavirus disease 2019 (COVID-19) in the routine diagnostic parasitology laboratory of a tertiary health care center. The risk assessment template included in the supplement of the interim guidance of "WHO Laboratory Biosafety Guidance Related to COVID-19" was used for the risk assessment. Risk assessments were carried out for the "diagnosis of protozoan diseases in respiratory tract samples" and "diagnosis of intestinal parasitic diseases" processes. Initial risk of the laboratory activities was determined before additional risk control measures and overall initial risk was estimated for each process. Overall residual risk of the laboratory activities after risk control measures was estimated for each process. Overall initial risk for both processes was "very high." Fresh microscopic examination steps in both processes and concentration steps for "diagnosis of intestinal parasite diseases" were discontinued. All aerosol-generating steps were moved into a class-IIA biological safety cabinet. Overall residual risk was "medium" for both processes. This study serves as an example for clinical laboratories regarding how the risk assessment approach in guidelines can be transferred to daily practice.

摘要

在本研究中,我们旨在进行生物安全风险评估,以确定在一家三级医疗保健中心的常规诊断寄生虫学实验室中针对2019冠状病毒病(COVID-19)应采取的措施。采用了《世界卫生组织与COVID-19相关的实验室生物安全指南》临时指南附录中的风险评估模板进行风险评估。对“呼吸道样本中原生动物疾病的诊断”和“肠道寄生虫疾病的诊断”过程进行了风险评估。在采取额外的风险控制措施之前确定了实验室活动的初始风险,并对每个过程的总体初始风险进行了估计。对每个过程在采取风险控制措施后的实验室活动总体残余风险进行了估计。两个过程的总体初始风险均为“非常高”。两个过程中的新鲜显微镜检查步骤以及“肠道寄生虫疾病诊断”的浓缩步骤均已停止。所有产生气溶胶的步骤都转移到了IIA级生物安全柜中。两个过程的总体残余风险均为“中等”。本研究为临床实验室提供了一个范例,说明指南中的风险评估方法如何应用于日常实践。

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