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      <title>Usefulness of a serial algorithm of HBsAg and HBeAg rapid diagnosis tests to detect pregnant women at risk of HBV mother-to-child transmission in Cambodia, the ANRS 12328 pilot study</title>
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    <abstract>Background: In Cambodia, access to hepatitis B surface antigen (HBsAg) screening is low for pregnant women and Hepatitis B Virus (HBV) DNA quantification is poorly accessible. Objectives: To evaluate the performance of a serial algorithm using two HBV rapid diagnostic tests (RDTs), in which samples positive for HBsAg were further tested for HBeAg as a surrogate marker for HBV DNA quantification. Study design: In 2015, we prospectively collected plasma samples from 250 pregnant women consulting for antenatal care in one hospital in Phnom Penh including 128 with a known positive HBsAg status. All specimens were tested with the SD BIOLINE HBsAg RDT and HBsAg ELISA assay. In ELISA-positive samples, HBeAg status was determined using the SD BIOLINE HBeAg RDT and HBV DNA quantification was assessed. Results: Sensitivity and specificity of HBsAg RDT were 99.2% (97.7-99.9) and 100% (97.0-100), respectively. Among the 128 ELISA-positive samples, 29 (23%) tested HBeAg positive and 34 (26.5%) had HBV DNA &gt; 5.3 Log(10) IU/mL. Sensitivity and specificity of HBeAg RDT in identifying viremic samples were 76.5% (62.2.0-90.7) and 96.8% (93.3-100) for HBV DNA &gt; 5.3 Log(10) IU/mL and 89.3% (77.8-100) and 96.0% (92.2-99.8) for HBV DNA &gt; 7.3 Log(10) IU/mL. Among the 99 negative HBeAg RDT women, 8 had HBV DNA &gt; 5.3 Log10 IU/mL and 7 of them harbored BCP/PC HBV mutants. Conclusions: A combination of HBsAg and HBeAg RDTs could be a low-cost strategy to identify HBV-infected pregnant women at risk of perinatal transmission in a country were HBV DNA quantification is not routinely available.</abstract>
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    <subject>
      <topic>Cambodia</topic>
      <topic>Hepatitis B virus</topic>
      <topic>Rapid diagnostic tests</topic>
      <topic>Pregnant women</topic>
      <topic>Mother-to-child transmission</topic>
    </subject>
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      <geographic>CAMBODGE</geographic>
    </subject>
    <classification authority="local">052</classification>
    <classification authority="local">050</classification>
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      <titleInfo>
        <title>Journal of Clinical Virology</title>
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      <part>
        <detail type="volume">
          <number>109</number>
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        <extent unit="pages">
          <list> 29-34</list>
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      <originInfo>
        <dateIssued>2018</dateIssued>
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      <identifier type="issn">1386-6532</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010074825</identifier>
    <identifier type="doi">10.1016/j.jcv.2018.10.007</identifier>
    <identifier type="issn">1386-6532</identifier>
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      <recordCreationDate encoding="w3cdtf">2019-02-04</recordCreationDate>
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