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临床实验室中免疫球蛋白和补体的delta检查初步研究。

The preliminary study of delta checks for immunoglobulins and complements in the clinical laboratory.

作者信息

Gong Xiangmei, He Shukang, Luo Li, Ding Chunyu, Qin Xin, Yuan Yilong, Cai Pengcheng, Yang Lihua

机构信息

Department of Clinical Laboratory, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Ann Clin Biochem. 2025 Mar;62(2):83-90. doi: 10.1177/00045632241287135. Epub 2024 Sep 24.

Abstract

BackgroundTo determine delta check limits for immunoglobulins and complements in outpatients and inpatients based on patient data and biological variation due to the lack of relevant studies.MethodsPatient data for IgA, IgG, IgM, IgE, C3, and C4 from 1 January 2022 to 31 December 2023 was collected from laboratory information system (LIS) in our clinical laboratory of Wuhan Union Hospital, which includes both outpatients and inpatients. The delta difference (DD), delta percent change (DPC), and reference change value (RCV) were calculated based on patient data and biological variation.ResultsFor DDs, there are significant differences between outpatients and inpatients in C4, IgE, IgG, and IgM. For DPCs, the corresponding analytes which are significantly different are C3, C4, IgE, IgG, and IgM. Two sources of CV to calculate the RCV of IgA, IgG, IgM, C3, and C4 were applied in this study, which revealed that two kinds of RCVs based on different biological variation databases are similar to each other, but both were smaller than delta check limits based on patient data, except for C4.ConclusionsThe delta check is a useful tool to monitor potential errors which may occur in total testing process. We hope our findings could be helpful for future studies focused on delta checks in immunological analytes.

摘要

背景

由于缺乏相关研究,基于患者数据和生物学变异来确定门诊患者和住院患者免疫球蛋白和补体的delta检查限值。

方法

收集武汉协和医院临床实验室2022年1月1日至2023年12月31日期间门诊和住院患者的IgA、IgG、IgM、IgE、C3和C4的患者数据。基于患者数据和生物学变异计算delta差异(DD)、delta百分比变化(DPC)和参考变化值(RCV)。

结果

对于DDs,门诊患者和住院患者在C4、IgE、IgG和IgM方面存在显著差异。对于DPCs,显著不同的相应分析物是C3、C4、IgE、IgG和IgM。本研究应用了两种CV来源来计算IgA、IgG、IgM、C3和C4的RCV,结果显示基于不同生物学变异数据库的两种RCV彼此相似,但除C4外,两者均小于基于患者数据的delta检查限值。

结论

delta检查是监测总检测过程中可能出现的潜在误差的有用工具。我们希望我们的研究结果能有助于未来专注于免疫分析物delta检查的研究。

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