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Evaluation of Zika rapid tests as aids for clinical diagnosis and epidemic preparedness
Global Health Impact Group, Atlanta, United States.
Institut Pasteur de Dakar, Dakar, Senegal.
Instituto Pedro Kouri, Havana, Cuba.
Institute Pasteur du Laos, Vientiane, Laos.
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2022 (English)In: eClinicalMedicine, E-ISSN 2589-5370, Vol. 49, article id 101478Article in journal (Refereed) Published
Abstract [en]

Background: Development and evaluation of diagnostics for diseases of epidemic potential are often funded during epidemics, but not afterwards, leaving countries unprepared for the next epidemic. United Nations Children's Emergency Fund (UNICEF) partnered with the United States Agency for International Development (USAID) to address this important gap by investing in an advance purchase commitment (APC) mechanism to accelerate the development and evaluation of Zika rapid diagnostic tests (RDTs) for case detection and surveillance. This paper describes the performance evaluation of five Zika RDTs eligible for procurement.

Methods: A network of European Union-funded ZikaPLAN sites in Africa, Asia, Latin America with access to relevant serum specimens were selected to evaluate RDTs developed for the UNICEF APC mechanism. A standardised protocol and evaluation panels were developed and a call for specimens for the evaluation panels issued to different sites. Each site contributed specimens to the evaluation from their biobank. Data were collated, analysed and presented to the UNICEF Procurement Review Group for review.

Findings: Three RDTs met the criteria for UNICEF procurement of sensitivity and specificity of 85% against a refence standard. The sensitivity/specificity of the ChemBio anti-Zika Virus (ZIKV) immunoglobulin M (IgM) test was 86.4 %/86.7% and the ChemBio ZCD system for anti-ZIKV IgM was 79.0%/97.1%, anti-dengue virus (DENV) IgM 90.0%/89.2%, anti-Chikungunya virus (CHIKV) IgM 90.6%/97.2%. The sensitivity/specificity of the SD Biosensor anti-ZIKV IgM was 96.8 %/90.8%, anti-DENV IgM 71.8%/83.5%, the DENV nonstructural protein 1 (NS1) glycoprotein 90.0%/90.2%, anti- yellow fever virus (YFV) IgM 84.6%/92.4%, anti-CHIKV IgM 86.3%/97.5%.

Interpretation: Three RDTs fulfilled the performance thresholds set by WHO and were eligible for UNICEF procurement. These tests will improve the diagnosis of ZIKV and other arboviral infections as well as providing countries with better tools for surveillance and response to future epidemics.

Place, publisher, year, edition, pages
Elsevier, 2022. Vol. 49, article id 101478
Keywords [en]
Advance purchase commitment, Biobanking network, Clinical medicine, Diagnostics, Epidemic preparedness, Evaluation, Zika
National Category
Infectious Medicine Public Health, Global Health and Social Medicine
Identifiers
URN: urn:nbn:se:umu:diva-196720DOI: 10.1016/j.eclinm.2022.101478ISI: 000829737900002Scopus ID: 2-s2.0-85131424183OAI: oai:DiVA.org:umu-196720DiVA, id: diva2:1671308
Funder
EU, Horizon 2020, 734584Available from: 2022-06-17 Created: 2022-06-17 Last updated: 2025-02-20Bibliographically approved

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Wilder-Smith, Annelies

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