<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1177/0004563220980495</dc:identifier><dc:language>eng</dc:language><dc:creator>Fabre, M.</dc:creator><dc:creator>Ruiz-Martinez, S.</dc:creator><dc:creator>Monserrat Cantera, M.E.</dc:creator><dc:creator>Cortizo Garrido, A.</dc:creator><dc:creator>Beunza Fabra, Z.</dc:creator><dc:creator>Peran, M.</dc:creator><dc:creator>Benito, R.</dc:creator><dc:creator>Mateo, P.</dc:creator><dc:creator>Paules, C.</dc:creator><dc:creator>Oros, D.</dc:creator><dc:title>SARS-CoV-2 immunochromatographic IgM/IgG rapid test in pregnancy: A false friend?</dc:title><dc:identifier>ART-2020-121660</dc:identifier><dc:description>Background: An increasing body of evidence has revealed that SARS-CoV-2 infection in pregnant women could increase the risk of adverse maternal and fetal outcomes. Careful monitoring of pregnancies with COVID-19 and measures to prevent neonatal infection are warranted. Therefore, rapid antibody tests have been suggested as an efficient screening tool during pregnancy. 
Cases: We analysed the clinical performance during pregnancy of a rapid, lateral-flow immunochromatographic assay for qualitative detection of SARS-CoV-2 IgG/IgM antibodies. We performed a universal screening including 169 patients during their last trimester of pregnancy. We present a series of 14 patients with positive SARS-CoV-2 immunochromatographic assay rapid test result. Immunochromatographic assay results were always confirmed by chemiluminescent microparticle immunoassays for quantitative detection of SARS-CoV-2 IgG and IgM+IgA antibodies as the gold standard. We observed a positive predictive value of 50% and a false positive rate of 50% in pregnant women, involving a significantly lower diagnostic performance than reported in non-pregnant patients. 
Discussion: Our data suggest that although immunochromatographic assay rapid tests may be a fast and profitable screening tool for SARS-CoV-2 infection, they may have a high false positive rate and low positive predictive value in pregnant women. Therefore, immunochromatographic assay for qualitative detection of SARS-CoV-2 IgG/IgM antibodies must be verified by other test in pregnant patients.</dc:description><dc:date>2020</dc:date><dc:source>http://zaguan.unizar.es/record/97463</dc:source><dc:doi>10.1177/0004563220980495</dc:doi><dc:identifier>http://zaguan.unizar.es/record/97463</dc:identifier><dc:identifier>oai:zaguan.unizar.es:97463</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/CM18-00202</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/JR19-00006</dc:relation><dc:identifier.citation>ANNALS OF CLINICAL BIOCHEMISTRY 58, 2 (2020), 149-152</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>