Suppr超能文献

中国 HIV-1 病毒载量检测实验室能力验证计划 2005-2019 十五年回顾。

Fifteen years of the proficiency testing program for HIV-1 viral load testing laboratories in China, 2005-2019.

机构信息

National AIDS Reference Laboratory, National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China.

National AIDS Reference Laboratory, National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China; Department of Epidemiology, School of Public Health, China Medical University, Shenyang, 110122, China.

出版信息

J Clin Virol. 2021 Sep;142:104911. doi: 10.1016/j.jcv.2021.104911. Epub 2021 Jul 14.

Abstract

BACKGROUND

HIV-1 viral load (VL) testing is essential for monitoring the effects of antiretroviral therapy in HIV-infected patients. In order to identify factors that impact testing performance of HIV-1 VL testing laboratories, this study performed a retrospective analysis on data from the domestic HIV-1 VL proficiency testing (PT) program in China during 2005 to 2019.

METHODS

Analysis was conducted on testing results of 155 PT panel specimens that were distributed to HIV-1 VL testing laboratories nationwide during 2005 to 2019. Follow-up on-site inspection records on unqualified laboratories were also analyzed.

RESULTS

By 2019, 267 HIV-1 VL testing laboratories in China enrolled in the national PT assessment. Overall, HIV-1 VL testing performance has been consistently good after 2012, with less than 5% of participants reporting an unqualified score. Unsatisfactory equipment conditions and poor laboratory administration were the two main reasons causing unqualified scores in the PT assessment. Interestingly, we found that HIV-1 VL testing laboratories had better performance in the CDC system than in hospitals. In analysis on the variance of specimen testing results by different assays, we found that variation in results existed across different assay platforms, and HIV-1 VL testing assays based on real-time PCR technology showed comparatively smaller inter-laboratory variability.

CONCLUSIONS

To maintain high performance in HIV-1 VL testing laboratories, it is important to strengthen laboratory management and preserve equipment conditions. Due to the variation of testing results among different assay platforms, we suggest using the same assay platform for longitudinal monitoring of patient viral load.

摘要

背景

HIV-1 病毒载量(VL)检测对于监测 HIV 感染者抗逆转录病毒治疗的效果至关重要。为了确定影响 HIV-1 VL 检测实验室检测性能的因素,本研究对 2005 年至 2019 年期间中国国内 HIV-1 VL 能力验证(PT)计划的数据进行了回顾性分析。

方法

对 2005 年至 2019 年期间分发给全国 HIV-1 VL 检测实验室的 155 个 PT 面板标本的检测结果进行了分析。同时还分析了对不合格实验室的后续现场检查记录。

结果

截至 2019 年,中国共有 267 家 HIV-1 VL 检测实验室参加了国家 PT 评估。总体而言,2012 年后 HIV-1 VL 检测性能一直良好,不合格分数低于 5%。设备条件不理想和实验室管理不善是导致 PT 评估不合格的两个主要原因。有趣的是,我们发现 HIV-1 VL 检测实验室在 CDC 系统中的表现优于医院。在对不同检测方法的标本检测结果进行方差分析时,我们发现不同检测平台的结果存在差异,基于实时 PCR 技术的 HIV-1 VL 检测方法表现出较小的实验室间变异性。

结论

为了保持 HIV-1 VL 检测实验室的高性能,加强实验室管理和维护设备条件非常重要。由于不同检测平台的检测结果存在差异,我们建议在对患者病毒载量进行纵向监测时使用相同的检测平台。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验