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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="bold" font="default" size="100%">Lallemant, Marc</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Le Coeur, Sophie</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sirirungsi, W.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Cressey, T. R.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Ngo-Giang-Huong, Nicole</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Traisathit, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Klinbuayaem, V.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sabsanong, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kanjanavikai, P.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Jourdain, Gonzague</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">McIntosh, K.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Koetsawang, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Phpt- Study Investigators</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Randomized noninferiority trial of two maternal single-dose nevirapine-sparing regimens to prevent perinatal HIV in Thailand</title>
        <secondary-title>Aids</secondary-title>
      </titles>
      <pages>2497-2507</pages>
      <keywords>
        <keyword>antiretroviral therapy</keyword>
        <keyword>clinical trial</keyword>
        <keyword>HIV</keyword>
        <keyword>prevention of mother-to-child transmission</keyword>
        <keyword>Thailand</keyword>
        <keyword>THAILANDE</keyword>
      </keywords>
      <dates>
        <year>2015</year>
      </dates>
      <call-num>fdi:010066091</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Aids</full-title>
      </periodical>
      <isbn>0269-9370</isbn>
      <accession-num>ISI:000368490200001</accession-num>
      <number>18</number>
      <electronic-resource-num>10.1097/qad.0000000000000865</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010066091</url>
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        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2016/02/010066091.pdf</url>
        </pdf-urls>
      </urls>
      <volume>29</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Objectives:Perinatal single-dose nevirapine (sdNVP) selects for resistance mutations. The objective of this trial was to compare two maternal sdNVP-sparing regimens with standard zidovudine (ZDV)/sdNVP prophylaxis.Design:PHPT-5 was a randomized, partially double-blind placebo-controlled, noninferiority trial in Thailand (NCT00409591). Study participants were women with CD4(+) of at least 250cells/l and their infants.Methods:All women received ZDV from 28 weeks' gestation and their newborn infants for one week. Women were also randomized to receive NVP-NVP (reference): maternal intrapartum sdNVP with a 7-day tail' of ZDV along with lamivudine, and infant NVP (one dose immediately, another 48h later); infant-only NVP: maternal placebos for sdNVP and the tail', with infant NVP; LPV/r: maternal LPV/r starting at 28 weeks. Infants were formula-fed. HIV-diagnosis was determined by DNA-PCR.Results:Four-hundred and thirty-five women were randomized between January 2009 and September 2010. Accrual was terminated prematurely following a change in Thai guidelines recommending antiretroviral combination therapy for all pregnant women. Data on 405 mothers and 407 live-born children were analyzed. Baseline characteristics were similar between arms. Intent-to-treat transmission rates were 3.8% (95% confidence interval: 1.2-8.6) in NVP-NVP, 1.6% (0.2-5.6) in infant-only NVP, and 1.4% (0.4-5.1) in LPV/r arms. As-treated rates were 2.2% (0.5-6.4), 3.2% (0.9-7.9), and 1.5% (0.2-5.2), respectively. Factors independently associated with transmission were prophylaxis duration less than 8 weeks (adjusted odds ratio 15.5; 3.6-66.1) and viral load at baseline at least 4log(10)copies/ml (adjusted odds ratio 10.9; 1.3-91.5). Regimens appeared well tolerated.Conclusion:Transmission rates in all arms were low but noninferiority was not proven. Antiretroviral prophylaxis for at least 8 weeks before delivery is necessary to minimize transmission risk.</abstract>
      <custom6>052 ; 050</custom6>
      <custom1>UR174 / UR196</custom1>
      <custom7>Thaïlande</custom7>
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