4.4 Article

Cost-effectiveness of first-line antiretroviral therapy for HIV-infected African children less than 3 years of age

Journal

AIDS
Volume 29, Issue 10, Pages 1247-1259

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0000000000000672

Keywords

Africa; cost-effectiveness; first-line antiretroviral therapy; IMPAACT; P1060 trial; pediatric HIV

Funding

  1. WHO
  2. National Institutes of Health through International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT)
  3. International Database to Evaluate AIDS (IeDEA)
  4. National Institute of Allergy and Infectious Diseases [K01 AI078754, R01 HD079214, K24 AI062476, R01 AI058736, R01 AI093269, U01 AI069911, U01AI09919]
  5. Harvard Center for AIDS Research
  6. March of Dimes Foundation
  7. Massachusetts General Hospital Executive Committee on Research
  8. National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH) (IMPAACT LOC) [UM1AI068632]
  9. National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH) (IMPAACT SDMC) [UM1AI068616]
  10. Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  11. National Institute of Mental Health (NIMH)
  12. National Institute of Allergy and Infectious Diseases (NIAID)
  13. NICHD [N01-DK-9-001/HHSN 267200800001C]
  14. National Cancer Institute

Ask authors/readers for more resources

Background:The International Maternal, Pediatric, and Adolescent Clinical Trials P1060 trial demonstrated superior outcomes for HIV-infected children less than 3 years old initiating antiretroviral therapy (ART) with lopinavir/ritonavir compared to nevirapine, but lopinavir/ritonavir is four-fold costlier.Design/methods:We used the Cost-Effectiveness of Preventing AIDS Complications (CEPAC)-Pediatric model, with published and P1060 data, to project outcomes under three strategies: no ART; first-line nevirapine (with second-line lopinavir/ritonavir); and first-line lopinavir/ritonavir (second-line nevirapine). The base-case examined South African children initiating ART at age 12 months; sensitivity analyses varied all key model parameters. Outcomes included life expectancy, lifetime costs, and incremental cost-effectiveness ratios [ICERs; dollars/year of life saved ($/YLS)]. We considered interventions with ICERs less than 1x per-capita gross domestic product (South Africa: $7500)/YLS as very cost-effective,' interventions with ICERs below 3x gross domestic product/YLS as cost-effective,' and interventions leading to longer life expectancy and lower lifetime costs as cost-saving'.Results:Projected life expectancy was 2.8 years with no ART. Both ART regimens markedly improved life expectancy and were very cost-effective, compared to no ART. First-line lopinavir/ritonavir led to longer life expectancy (28.8 years) and lower lifetime costs ($41350/person, from lower second-line costs) than first-line nevirapine (27.6 years, $44030). First-line lopinavir/ritonavir remained cost-saving or very cost-effective compared to first-line nevirapine unless: liquid lopinavir/ritonavir led to two-fold higher virologic failure rates or 15-fold greater costs than in the base-case, or second-line ART following first-line lopinavir/ritonavir was very ineffective.Conclusions:On the basis of P1060 data, first-line lopinavir/ritonavir leads to longer life expectancy and is cost-saving or very cost-effective compared to first-line nevirapine. This supports WHO guidelines, but increasing access to pediatric ART is critical regardless of the regimen used.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available