Table 3.
Sensitivity analysis results.
ART strategy (ordered by costs)a | Undiscounted LE (years) | Discounted LE (years) | Discounted lifetime costs | ICER ($/life-years saved) |
Alternative patient populations and healthcare costs | ||||
South Africa: in-utero/intrapartum infection; presenting age 6 months | ||||
No ART | 2.50 | 2.23 | 8520 | |
First-line LPV/r | 27.45 | 16.31 | 20 620 | 860 |
First-line NVP | 26.29 | 15.81 | 21 960 | Dominatedb |
South Africa: in-utero/intrapartum infection; presenting age 24 monthsc | ||||
No ART | 3.54 | 3.09 | 12 670 | |
First-line LPV/r | 28.71 | 17.10 | 27 220 | 710 |
First-line NVP | 27.52 | 16.59 | 29 600 | Dominated |
South Africa: in-utero/intrapartum infection; presenting age 35 monthsc | ||||
No ART | 4.71 | 4.03 | 14 420 | |
First-line LPV/r | 29.46 | 17.60 | 23 240 | 650 |
First-line NVP | 28.36 | 17.11 | 24 790 | Dominated |
Côte d’Ivoire: in-utero/intrapartum infection; presenting age 12 monthsd | ||||
No ART | 2.83 | 2.52 | 1820 | |
First-line LPV/r | 28.79 | 17.11 | 15 120 | 910 |
First-line NVP | 27.62 | 16.58 | 15 480 | Dominated |
Additional sensitivity analyses (South Africa, in-utero/intrapartum infection; presenting age 12 months) | ||||
One line of ART available | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line NVPa | 22.42 | 14.57 | 24 890 | 1210 |
First-line LPV/r | 23.84 | 15.31 | 26 490 | 2190 |
Stop second-line ART at failure | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line NVPa | 23.76 | 15.03 | 17 360 | 565 |
First-line LPV/r | 25.18 | 15.74 | 17 760 | 570 |
PENPACT-1 ART efficacies | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line LPV/r | 29.28 | 16.96 | 22 240 | Weakly dominatede |
First-line NVP | 30.42 | 17.39 | 22 370 | 810 |
Second-line NNRTI efficacy (40%) | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line LPV/r | 26.51 | 16.26 | 23 010 | 930 |
First-line NVP | 27.61 | 16.59 | 23 370 | 1110 |
2.1× late failure for first-line LPV/r (1.9%/month)f | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line LPV/r | 26.60 | 16.38 | 22 070 | 850 |
First-line NVP | 27.61 | 16.59 | 23 370 | 6310 |
4.5× cost of liquid LPV/r ($80–105 per month for children <3 years of age) | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line NVPa | 28.77 | 16.59 | 23 480 | Weakly dominated |
First-line LPV/r | 27.58 | 17.10 | 23 510 | 910 |
15.0× cost of liquid LPV/r ($260–330 per month for children <3 years of age) | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line NVPa | 27.58 | 16.58 | 23 780 | 960 |
First-line LPV/r | 28.79 | 17.09 | 28 170 | 8640 |
Liquid LPV/r used until age 5 | ||||
No ART | 2.83 | 2.52 | 10 290 | |
First-line LPV/r | 28.77 | 17.09 | 22 730 | 850 |
First-line NVP | 27.59 | 16.60 | 23 440 | Dominated |
Costs are in 2012 USD. Discounting is at 3% per year (results using alternative discount rates are shown in the Appendix (http://links.lww.com/QAD/A686). ART, antiretroviral therapy; DRV/r, darunavir/ritonavir; ICER, incremental cost-effectiveness ratio; LE, life expectancy; LPV/r, lopinavir/ritonavir; NNRTI, nonnucleoside reverse transcriptase inhibitor; NVP, nevirapine.
aStrategies are listed in order of increasing costs. As a result, the order of the three treatment strategies changes between scenarios. Scenarios in which first-line NVP is less expensive over a lifetime horizon than first-line LPV/r are highlighted with footnote (a).
b‘Dominated’ in this table refers to strong dominance: a strategy is both more expensive and less effective than its next less expensive alternative.
cIn these analyses, the model simulates a cohort of children presenting to care and initiating ART at ages 6, 12, 24, and 35 months. Morbidity and mortality occurring among children before these ages are not included in these analyses. As a result, children presenting to care at older ages have longer projected life expectancies both with and without ART. This occurs because the model incorporates age-stratified mortality risks from HIV and non-HIV causes. High mortality rates among young, untreated children mean that children who survive without treatment to present to care at older ages are generally less sick, reflecting the ‘survivor bias’ seen in most cohorts of HIV-infected children [16–18]. These analyses are intended to evaluate the impact of age at ART initiation on the comparison between the two first-line regimens, and not to compare the outcomes of early versus delayed ART initiation.
dBase-case results using Côte d’Ivoire costs are shown here. Full results for all analyses using Côte d’Ivoire costs are in the Appendix (http://links.lww.com/QAD/A686).
eWeakly dominated. Here, refers to extended dominance: the incremental cost-effectiveness ratio (ICER) of the nondominated strategy compared to the dominated strategy is less than the ICER of the dominated strategy compared to no ART, indicating that the dominated strategy is an inefficient use of healthcare resources.
fIn this scenario, we model a higher risk of late virologic failure (after initial suppression) for lopinavir/ritonavir in first-line ART, but no increase in late failure for nevirapine in first-line ART or for either second-line regimen. Such a scenario might occur if liquid lopinavir/ritonavir (administered to children too young to swallow pills) is much more difficult to tolerate than all other modeled regimens.