<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" 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:title>Cost-effectiveness of three alternative boosted Protease inhibitor-based second-line regimens in HIV-infected patients in West and Central Africa</dc:title>
  <dc:creator>Boyer, S.</dc:creator>
  <dc:creator>Nishimwe, M. L.</dc:creator>
  <dc:creator>/Sagaon Teyssier, Luis</dc:creator>
  <dc:creator>/March, Laura</dc:creator>
  <dc:creator>Koulla-Shiro, S.</dc:creator>
  <dc:creator>Bousmah, M. Q.</dc:creator>
  <dc:creator>Toby, R.</dc:creator>
  <dc:creator>Mpoudi-Etame, M. P.</dc:creator>
  <dc:creator>Gueye, N. F. N.</dc:creator>
  <dc:creator>Sawadogo, A.</dc:creator>
  <dc:creator>Kouanfack, C.</dc:creator>
  <dc:creator>Ciaffi, L.</dc:creator>
  <dc:creator>Spire, B.</dc:creator>
  <dc:creator>Delaporte, E.</dc:creator>
  <dc:description>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.</dc:description>
  <dc:date>2020</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010077924</dc:identifier>
  <dc:identifier>fdi:010077924</dc:identifier>
  <dc:identifier>Boyer S., Nishimwe M. L., Sagaon Teyssier Luis, March Laura, Koulla-Shiro S., Bousmah M. Q., Toby R., Mpoudi-Etame M. P., Gueye N. F. N., Sawadogo A., Kouanfack C., Ciaffi L., Spire B., Delaporte E.. Cost-effectiveness of three alternative boosted Protease inhibitor-based second-line regimens in HIV-infected patients in West and Central Africa. 2020, 4 (1),  45-60</dc:identifier>
  <dc:language>EN</dc:language>
  <dc:coverage>BURKINA FASO</dc:coverage>
  <dc:coverage>CAMEROUN</dc:coverage>
  <dc:coverage>SENEGAL</dc:coverage>
</oai_dc:dc>
