Diagnostic performances of Exacto® Triplex rapid test for diagnosis of HIV/HCV/HBsAg: a multicenter, cross-sectional, field study in the Central African Republic.

The Pan African Medical Journal Pub Date : 2022-09-14 eCollection Date: 2022-01-01 DOI:10.11604/pamj.2022.43.21.36041
Christian Diamant Mossoro-Kpinde, Ginette Claude Mireille Kalla, Coretha Baguida-Bokia, Simplice Sombot-Ndicki, Christelle Bobossi, Serge Tonen-Wolyec, François-Xavier Mbopi-Kéou, Laurent Bélec
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引用次数: 0

Abstract

Introduction: the Exacto® Triplex HIV/HCV/HBsAg (Biosynex, Strasbourg, France) consists in lateral flow, immunochromatographic rapid diagnostic test simultaneously detecting human immunodeficiency virus (HIV)-1 and HIV-2 and hepatitis C virus (HCV)- specific antibodies (IgG and IgM) and hepatitis B virus (HBV) surface antigen (HBsAg) in serum, plasma and whole blood. We herein evaluated its diagnostic performances in the Central African Republic (CAR).

Methods: cross-sectional study was conducted on prospectively collected panel of 550 sera from adult inpatients living in Bangui, including 200 HIV-positive, 100 HBsAg-positive, 50 HCV-positive, 200 negatives to three viruses according to reference immuno-enzymatic serological tests including Murex HCV (Diasorin, Saluggia, Italy) for HCV, Murex HBsAg (Diasorin) for HBV, Genscreen ULTRA HIV Ag-Ab HIV-1/2 Version 2 (Bio-Rad, Marnes-la-Coquette, France) and Murex HIV 1.2.0 Ag/Ab Combination (Diasorin), the 2 tests associated in the parallel algorithm for the reference strategy for the diagnosis of HIV in CAR. Serum samples were tested blindly in duplicate. The findings are reported following the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines.

Results: the Exacto® Triplex showed 99.5% (95% CI; 98.5-100.0), 96.0% [90.6-100.0] and 99.0% [97.1-100.0] sensitivities for HIV, HCV and HBsAg, respectively. The specificity, positive and negative predictive values (PPV and NPV) were 100.0% for all three viruses. The Youden's J index and Cohen's κ coefficient were 0.99 for HIV and HBsAg. For HCV, Youden's J and Cohen's κ coefficient were 0.96 and 0.98, respectively. In the epidemiological context of the CAR, the PPV and NPV for all three viral infections were high (≥99.0% to 100%).

Conclusion: taken together, our STROBE-compliant study demonstrates that the Exacto® Triplex HIV/HCV/HBsAg showed high sensitivity and specificity for HIV and HBsAg (≥99.0%), and relatively high sensitivity (96.0%) and high specificity (100%) for HCV. These analytical performances are within the limits required by the WHO (i.e. sensitivity ≥99.0% and specificity ≥98.0%) for HIV and HBV. The Exacto® Triplex HIV/HCV/HBsAg is user-friendly at low cost, and appears highly desirable for routine use in the CAR, and likely other Central African countries.

用于诊断HIV/HCV/HBsAg的Exacto®Triplex快速检测的诊断性能:中非共和国一项多中心、横断面的实地研究
简介:Exacto®Triplex HIV/HCV/HBsAg (Biosynex, Strasbourg, France)是一种横向流动、免疫层析快速诊断试剂盒,可同时检测血清、血浆和全血中的人类免疫缺陷病毒(HIV)-1和HIV-2以及丙型肝炎病毒(HCV)特异性抗体(IgG和IgM)和乙型肝炎病毒(HBV)表面抗原(HBsAg)。我们在此评估其诊断性能在中非共和国(CAR)。方法:本研究前瞻性收集班吉市成年住院患者血清550份,其中HIV阳性200份、HBsAg阳性100份、HCV阳性50份、HCV阴性200份,采用参考免疫酶血清检测方法,包括HCV检测Murex HCV(意大利Saluggia)、HBV检测Murex HBsAg (Diasorin)、Genscreen ULTRA HIV Ag-Ab HIV-1/2 Version 2(法国mares -la- coquette Bio-Rad)和HIV 1.2.0 Ag/Ab Combination (Diasorin)。并行算法中相关的两项检测为CAR病毒诊断参考策略。血清样本一式两份盲测。这些发现是根据加强流行病学观察性研究报告(STROBE)指南报道的。结果:Exacto®Triplex显示99.5% (95% CI;98.5-100.0)、96.0%[90.6-100.0]和99.0%[97.1-100.0]对HIV、HCV和HBsAg的敏感性。三种病毒的特异性、阳性预测值和阴性预测值(PPV和NPV)均为100.0%。HIV和HBsAg的Youden’s J指数和Cohen’s κ系数均为0.99。HCV的Youden’s J和Cohen’s κ系数分别为0.96和0.98。在CAR的流行病学背景下,所有三种病毒感染的PPV和NPV都很高(≥99.0%至100%)。结论:总的来说,我们的strobe依从性研究表明,Exacto®Triplex HIV/HCV/HBsAg对HIV和HBsAg具有较高的敏感性和特异性(≥99.0%),对HCV具有相对较高的敏感性(96.0%)和高特异性(100%)。这些分析性能均在WHO对HIV和HBV要求的限度内(即灵敏度≥99.0%,特异性≥98.0%)。Exacto®Triplex HIV/HCV/HBsAg易于使用,成本低,在中非共和国和其他中非国家似乎非常适合常规使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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