Clinical performance evaluation of an HIV Duo assay: From HIV screening to acute and non-acute HIV infection detection

IF 3.2 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinica Chimica Acta Pub Date : 2024-09-04 DOI:10.1016/j.cca.2024.119949
Xin Liu , Chongyang Wu , Yulin Yuan , Dongdong Li , Jinli Lou , Xia Feng , Qiuwei Lu , Rongcai Wu , An-Jou Chen , Chuanmin Tao
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Abstract

Background

Evaluating the clinical performance of Elecsys HIV Duo assay for primary human immunodeficiency virus (HIV) screening and acute HIV infection detection.

Methods

This study was conducted from April 2022 to April 2023 and involved two distinct populations. For the HIV screening population, three HIV Duo results [HIV Duo, HIV antigen (Ag), and HIV antibody (Ab)] in primary screening were obtained (January 2021 to June 2021). In the diagnosed HIV population, retrospective samples from November 2016 to March 2023 were measured.

Results

The HIV screening population included 111,383 samples from a real-world screening program. The assay demonstrated a specificity of 99.91 % (95 % CI: 99.89 %, 99.93 %) and a PPV of 0.8516 (95 % CI: 0.8225, 0.8776). Regarding the diagnosed HIV population, 836 HIV patients were enrolled, including 14 acute HIV infectious patients with only HIV Ag + and a Western Blot (WB) confirmation rate of 0 %. The median (IQR) of the numeric cut-off index (COI) ratios of HIV Duo Ab and Ag significantly differed among the Ag + Ab-, Ag-Ab+, and Ag + Ab + subgroups.

Conclusion

The Elecsys HIV Duo assay is suitable for primary HIV screening and can be integrated into a novel laboratory HIV testing algorithm to improve acute HIV detection in Chinese clinical practice.

Abbreviations: HIV, Human immunodeficiency virus; AIDS, acquired immunodeficiency syndrome; Ag, antigen; Ab, antibody; WB, Western Blot; COI, numeric cut-off index; CI, confidence interval; NAT, nucleic acid tests; EDC, electronic data capture systems; CDC, Chinese Centers for Disease Control and Prevention; IQR, interquartile range; PPV, positive predictive value; HCV, hepatitis C virus; HBV, hepatitis B virus; CI, confidence interval; ND, not able to define; F, female; M, male;

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HIV Duo 检测法的临床性能评估:从 HIV 筛查到急性和非急性 HIV 感染检测。
背景:评估 Elecsys HIV Duo 检测试剂盒用于人类免疫缺陷病毒(HIV)初筛和急性 HIV 感染检测的临床性能:评估 Elecsys HIV Duo 检测试剂盒在人类免疫缺陷病毒(HIV)初筛和急性 HIV 感染检测中的临床性能:本研究于 2022 年 4 月至 2023 年 4 月进行,涉及两个不同的人群。对于 HIV 筛查人群,在初筛(2021 年 1 月至 2021 年 6 月)中获得了三个 HIV Duo 结果[HIV Duo、HIV 抗原(Ag)和 HIV 抗体(Ab)]。在确诊的艾滋病人群中,测量了 2016 年 11 月至 2023 年 3 月的回顾性样本:结果:HIV 筛查人群包括来自真实世界筛查项目的 111,383 份样本。检测的特异性为 99.91 %(95 % CI:99.89 %,99.93 %),PPV 为 0.8516(95 % CI:0.8225,0.8776)。在确诊的艾滋病毒感染者中,有 836 名艾滋病毒感染者,其中包括 14 名只有 HIV Ag + 的急性艾滋病毒感染者,Western Blot (WB) 确认率为 0%。在 Ag + Ab-、Ag-Ab+ 和 Ag + Ab + 亚组中,HIV Duo Ab 和 Ag 的数字截断指数 (COI) 比值的中位数(IQR)有显著差异:结论:Elecsys HIV Duo 检测试剂盒适用于 HIV 初筛,可纳入新型实验室 HIV 检测算法,以提高中国临床实践中的急性 HIV 检测水平:缩写: HIV,人类免疫缺陷病毒;AIDS,获得性免疫缺陷综合征;Ag,抗原;Ab,抗体;WB,Western Blot;COI,数字截断指数;CI,置信区间;NAT,核酸检测;EDC,电子数据采集系统;CDC,中国疾病预防控制中心;IQR,四分位数区间;PPV,阳性预测值;HCV,丙型肝炎病毒;HBV,乙型肝炎病毒;CI,置信区间;ND,无法定义;F,女性;M,男性。
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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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