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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%">Denoeud Ndam, Lise</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Clément, M. C.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Briand, Valérie</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Akakpo, J.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Agossou, V. K.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Atadokpédé, F.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Dossou-Gbété, L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Komongui, D. G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Afangnihoun, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Girard, P. M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Zannou, D. M.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Cot, Michel</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Tolerability of mefloquine intermittent preventive treatment for malaria in HIV-infected pregnant women in Benin</title>
        <secondary-title>Jaids-Journal of Acquired Immune Deficiency Syndromes</secondary-title>
      </titles>
      <pages>64-72</pages>
      <keywords>
        <keyword>HIV</keyword>
        <keyword>malaria</keyword>
        <keyword>pregnancy</keyword>
        <keyword>mefloquine</keyword>
        <keyword>drug tolerance</keyword>
        <keyword>Benin</keyword>
      </keywords>
      <dates>
        <year>2012</year>
      </dates>
      <call-num>fdi:010057157</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Jaids-Journal of Acquired Immune Deficiency Syndromes</full-title>
      </periodical>
      <isbn>1525-4135</isbn>
      <accession-num>ISI:000308352000015</accession-num>
      <number>1</number>
      <electronic-resource-num>10.1097/QAI.0b013e3182615a58</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010057157</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2012/09/010057157.pdf</url>
        </pdf-urls>
      </urls>
      <volume>61</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Objective: To investigate the tolerability of mefloquine intermittent preventive treatment (MQ IPTp) for malaria in HIV-infected pregnant women compared with HIV-negative women. Design: Prospective cohort study comparing samples of HIV-negative and HIV- infected pregnant women from 2 clinical trials conducted in Benin. Methods: One hundred and three HIV-infected women from the ongoing PACOME trial were compared with 421 HIV-negative women from a former trial, both trials aiming to evaluate the efficacy and tolerability of MQ IPTp, administered at the dose of 15 mg/kg. Descriptive analysis compared the proportion of women reporting at least 1 adverse reaction, according to HIV status. Multilevel logistic regression identified factors associated with the probability of reporting an adverse reaction for each MQ intake. Results: Dizziness and vomiting were the most frequent adverse reactions. Adverse reactions were less frequent in HIV-infected women (65% versus 78%, P = 0.009). In multilevel analysis, HIV infection [odds ratio (OR) = 0.23, 95% confidence interval (CI) = 0.08 to 0.61] decreased the risk for adverse reactions, whereas detectable viral load (OR = 2.46, 95% CI = 1.07 to 5.66), first intake (versus further intakes, OR = 5.26, 95% CI = 3.70 to 7.14), older age (OR = 1.62, 95% CI = 1.13 to 2.32), and higher education level (OR = 1.71, 95% CI = 1.12 to 2.61) increased the risk. Moderate and severe adverse reactions were more frequent when antiretrovirals were started concomitantly with a MQ intake. Conclusions: This study provides reassuring data on the use of MQ IPTp in HIV-infected pregnant women. However frequent, adverse reactions remained moderate and did not impair adherence to MQ IPTp. In this high-risk group, MQ might be an acceptable alternative in case sulfadoxine-pyrimethamine loses its efficacy for intermittent preventive treatment.</abstract>
      <custom6>052 ; 050</custom6>
      <custom1>UR216</custom1>
      <custom7>Bénin</custom7>
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