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在中国进行 Xpert HIV-1 病毒载量测定法用于 HIV 定量的多中心评估。

Multicenter evaluation of Xpert HIV-1 viral load assay for HIV quantification in China.

机构信息

Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Beijing Key Laboratory for HIV/AIDS Research, Beijing, China.

出版信息

J Med Virol. 2020 Dec;92(12):3295-3300. doi: 10.1002/jmv.26295. Epub 2020 Jul 27.

Abstract

New approaches to increase HIV-1 testing and HIV-1 viral load (VL) monitoring are needed for people living with HIV (PLHIV) in China. The Xpert HIV-1 VL assay was prequalified by the World Health Organization in 2017 but has not been evaluated in China. A multicenter evaluation was conducted to assess the accuracy of the Cepheid Xpert HIV-1 VL assay compared to the Abbott RealTime HIV-1 assay in China. Overall agreement was seen in 558 of 562 specimens (99.29%) with a κ value of 0.962. Pearson's coefficient between the two assays was 0.943. Analyzed by the Bland-Altman method, the mean bias was -0.54 log  copies/mL, and 94.05% results fell within the 95% confidence limit of agreement (-1.248 to 0.168 log  copies/mL). The coefficient of variation of the Cepheid Xpert HIV-1 VL assay ranged from 0.61% to 1.55%, as determined by testing eight positive plasma specimens with three different lots on different days. Due to its simplicity, random-access, rapid turnaround time, and accuracy, the Xpert HIV-1 VL assay can be used in local hospitals and clinics that bear the burden of identifying and treating HIV patients in China.

摘要

在中国,需要为 HIV 感染者(PLHIV)寻找新的方法来增加 HIV-1 检测和 HIV-1 病毒载量(VL)监测。Cepheid 的 Xpert HIV-1 VL 检测法于 2017 年被世界卫生组织预认证,但尚未在中国进行评估。进行了一项多中心评估,以评估 Cepheid Xpert HIV-1 VL 检测法与 Abbott RealTime HIV-1 检测法在中国的准确性。562 个标本中有 558 个(99.29%)标本的总体一致性较好,κ 值为 0.962。两种检测方法之间的皮尔逊相关系数为 0.943。通过 Bland-Altman 方法分析,平均偏差为 -0.54 log 拷贝/ml,94.05%的结果在 95%置信区间内(-1.248 至 0.168 log 拷贝/ml)。通过对 8 个不同批次的阳性血浆标本在不同天进行 3 次检测,Cepheid Xpert HIV-1 VL 检测法的变异系数为 0.61%至 1.55%。由于其简单、随机访问、快速周转时间和准确性,Xpert HIV-1 VL 检测法可用于中国当地医院和诊所,以识别和治疗 HIV 患者。

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