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用于支持南非抗逆转录病毒治疗监测的Xpert HIV-1病毒载量检测的标准化质量评估材料的开发

The Development of a Standardized Quality Assessment Material to Support Xpert HIV-1 Viral Load Testing for ART Monitoring in South Africa.

作者信息

Noble Lara Dominique, Scott Lesley Erica, Bongwe Asiashu, Da Silva Pedro, Stevens Wendy Susan

机构信息

Department of Molecular Medicine and Haematology, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2000, Gauteng, South Africa.

National Priority Program, National Health Laboratory Service, Johannesburg 2000, Gauteng, South Africa.

出版信息

Diagnostics (Basel). 2021 Jan 22;11(2):160. doi: 10.3390/diagnostics11020160.

Abstract

The tiered laboratory framework for human immunodeficiency virus (HIV) viral load monitoring accommodates a range of HIV viral load testing platforms, with quality assessment critical to ensure quality patient testing. HIV plasma viral load testing is challenged by the instability of viral RNA. An approach using an RNA stabilizing buffer is described for the Xpert HIV-1 Viral Load (Cepheid) assay and was tested in remote laboratories in South Africa. Plasma panels with known HIV viral titres were prepared in PrimeStore molecular transport medium for per-module verification and per-instrument external quality assessment. The panels were transported at ambient temperatures to 13 testing laboratories during 2017 and 2018, tested according to standard procedures and uploaded to a web portal for analysis. A total of 275 quality assessment specimens (57 verification panels and two EQA cycles) were tested. All participating laboratories met study verification criteria ( = 171 specimens) with an overall concordance correlation coefficient (ρ) of 0.997 (95% confidence interval (CI): 0.996 to 0.998) and a mean bias of -0.019 log copies per milliliter (cp/mL) (95% CI: -0.044 to 0.063). The overall EQA ρ ( = 104 specimens) was 0.999 (95% CI: 0.998 to 0.999), with a mean bias of 0.03 log cp/mL (95% CI: 0.02 to 0.05). These panels are suitable for use in quality monitoring of Xpert HIV-1 VL and are applicable to laboratories in remote settings.

摘要

用于人类免疫缺陷病毒(HIV)病毒载量监测的分级实验室框架涵盖了一系列HIV病毒载量检测平台,质量评估对于确保患者检测质量至关重要。HIV血浆病毒载量检测受到病毒RNA不稳定性的挑战。本文描述了一种使用RNA稳定缓冲液的方法用于Xpert HIV-1病毒载量(Cepheid)检测,并在南非的偏远实验室进行了测试。在PrimeStore分子转运培养基中制备了具有已知HIV病毒滴度的血浆样本板,用于每个模块的验证和每个仪器的外部质量评估。这些样本板在2017年和2018年期间在环境温度下运送到13个检测实验室,按照标准程序进行检测,并上传到门户网站进行分析。共检测了275个质量评估样本(57个验证样本板和两个EQA周期)。所有参与实验室均符合研究验证标准( = 171个样本),总体一致性相关系数(ρ)为0.997(95%置信区间(CI):0.996至0.998),平均偏差为-0.019 log拷贝每毫升(cp/mL)(95% CI:-0.044至0.063)。总体EQA ρ( = 104个样本)为0.999(95% CI:0.998至0.999),平均偏差为0.03 log cp/mL(95% CI:0.02至0.05)。这些样本板适用于Xpert HIV-1 VL的质量监测,适用于偏远地区的实验室。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d1e/7911816/e7e4ff49c7a4/diagnostics-11-00160-g001.jpg

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