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比利时艾滋病参考实验室进行的一项盲法多中心质量控制研究,用于定量检测血浆中1型人类免疫缺陷病毒RNA 。

Blinded, multicenter quality control study for the quantification of human immunodeficiency virus type 1 RNA in plasma by the Belgian AIDS reference laboratories.

作者信息

Muyldermans G, Debaisieux L, Fransen K, Marissens D, Miller K, Vaira D, Vandamme A M, Vandenbroucke A T, Verhofstede C, Schuurman R, Zissis G, Lauwers S

机构信息

Belgian AIDS Reference Laboratories, Academisch Ziekenhuis - Vrije Universiteit Brussel, Brussels; Universiteé Libre de Bruxelles, Brussels.

出版信息

Clin Microbiol Infect. 2000 Apr;6(4):213-7. doi: 10.1046/j.1469-0691.2000.00048.x.

Abstract

OBJECTIVE

In order to evaluate the interlaboratory variation of HIV-1 RNA measurements in plasma, the Belgian AIDS reference laboratories organized a blinded multicenter quality control study.

METHODS

Atest panel of coded spiked HIV-1 plasma samples reflecting the dynamic range of the assay was composed and distributed. The HIV-1 RNA concentration of these samples was determined by the eight Belgian AIDS reference laboratories by means of the Amplicor HIV-1 Monitor version 1.5 assay.

RESULTS

Analysis of the results demonstrated that there was little interlaboratory variation for the high concentration range (4.0-5.7 log10 copies/mL), never exceeding 0.2 log10 copies/mL. However the standard deviation for the low concentration range (2.6-3.9 log10 copies/mL) reached up to 0.22 log10 copies/mL.

CONCLUSIONS

Since interlaboratory variability never reached 0.5 log10 copies/mL and each of the laboratories was able to detect four-fold differences in plasma HIV-1 RNA levels, the Amplicor assay can be used in multicenter studies without a centralized analysis of samples. Furthermore, this well-characterized proficiency panel of spiked plasma samples could be used as a standard in the study of interassay comparisons.

摘要

目的

为评估血浆中HIV-1 RNA检测的实验室间差异,比利时艾滋病参考实验室组织了一项盲法多中心质量控制研究。

方法

构建并分发了一组编码的加标HIV-1血浆样本检测面板,其反映了检测方法的动态范围。这八个比利时艾滋病参考实验室采用Amplicor HIV-1 Monitor 1.5版检测方法测定了这些样本的HIV-1 RNA浓度。

结果

结果分析表明,高浓度范围(4.0 - 5.7 log10拷贝/毫升)的实验室间差异很小,从未超过0.2 log10拷贝/毫升。然而,低浓度范围(2.6 - 3.9 log10拷贝/毫升)的标准差高达0.22 log10拷贝/毫升。

结论

由于实验室间变异从未达到0.5 log10拷贝/毫升,且每个实验室都能够检测出血浆HIV-1 RNA水平的四倍差异,因此Amplicor检测方法可用于多中心研究,而无需对样本进行集中分析。此外,这个特征明确的加标血浆样本能力验证检测面板可作为检测方法间比较研究的标准。

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