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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="normal" font="default" size="100%">Boyer, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Nishimwe, M. L.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Sagaon Teyssier, Luis</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">March, Laura</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Koulla-Shiro, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bousmah, M. Q.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Toby, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Mpoudi-Etame, M. P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Gueye, N. F. N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sawadogo, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kouanfack, C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ciaffi, L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Spire, B.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Delaporte, E.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Cost-effectiveness of three alternative boosted Protease inhibitor-based second-line regimens in HIV-infected patients in West and Central Africa</title>
        <secondary-title>Pharmacoeconomics-Open</secondary-title>
      </titles>
      <pages>45-60</pages>
      <keywords>
        <keyword>BURKINA FASO</keyword>
        <keyword>CAMEROUN</keyword>
        <keyword>SENEGAL</keyword>
      </keywords>
      <dates>
        <year>2020</year>
      </dates>
      <call-num>fdi:010077924</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Pharmacoeconomics-Open</full-title>
      </periodical>
      <isbn>2509-4262</isbn>
      <accession-num>ISI:000513273400006</accession-num>
      <number>1</number>
      <electronic-resource-num>10.1007/s41669-019-0157-9</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010077924</url>
        </related-urls>
        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers20-04/010077924.pdf</url>
        </pdf-urls>
      </urls>
      <volume>4</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background While dolutegravir has been added by WHO as a preferred second-line option for the treatment of HIV infection, boosted protease inhibitor (bPI)-based regimens are still needed as alternative second-line options. Identifying optimal bPI-based second-line combinations is essential, given associated high costs and funding constraints in low- and middle-income countries. We assessed the cost-effectiveness of three alternative bPI-based second-line regimens in Burkina Faso, Cameroon and Senegal. Methods We used data collected over 2010-2015 in the 2LADY trial/post-trial cohort. Patients with first-line antiretroviral therapy (ART) failure were randomly assigned to tenofovir/emtricitabine + lopinavir/ritonavir (TDF/FTC LPV/r; arm A), abacavir + didanosine + lopinavir/ritonavir (arm B), or tenofovir/emtricitabine + darunavir/ritonavir (arm C). Costs (US dollars, 2016), quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratios were computed for each country over 24 months of follow-up and extrapolated to 5 years using a simulated patient-level Markov model. We assessed uncertainty using cost-effectiveness acceptability curves, scenarios and prices threshold analysis. Results In each country, over 24 months, arm A was significantly less costly than arms B and C (incremental costs ranging from US$410-$US721 and US$468-US$546 for B and C vs A, respectively) and offered similar health benefits (incremental QALY: - 0.138 to 0.023 and - 0.179 to 0.028, respectively). Over 5 years, arm A remained the least costly, health benefits not being significantly different between arms. Compared with arms B and C, in each study country, Arm A had a &gt;= 95% probability of being cost-effective for a large range of cost-effectiveness thresholds, irrespective of the scenario considered. Conclusions Using TDF/FTC LPV/r as a bPI-based second-line regimen provided the best economic value in the three study countries.</abstract>
      <custom6>056</custom6>
      <custom1>UR259 / UR233</custom1>
      <custom7>Burkina Faso / Cameroun / Sénégal</custom7>
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