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. Author manuscript; available in PMC: 2008 May 5.
Published in final edited form as: AIDS. 2007 May 11;21(8):973–982. doi: 10.1097/QAD.0b013e328011ec53

Table 3.

Sensitivity analysis of key model input parameters and baseline assumptionsa.

Treatment strategy Undiscounted life expectancy NNRTI → PI (years) Undiscounted life expectancy PI → NNRTI (years) Cost-effectiveness ratio ($/year of life saved)a NNRTI resistance prevalence (%) where cost-effective to use PI → NNRTIb
Base case 8.89 7.99 910 76
ART starting criteria:
 CD4 cell count
 < 350 cells/μl or one
 opportunistic infectionc
9.42 8.49 930 76
ART starting criteria:
 CD4 cell count
 < 200 cells/ml or four
 opportunistic infection
or CD4 cell count
 < 350 cells/μl and one
 opportunistic infectionc
8.49 7.61 890 78
First-line ART failure criteria:
 CD4 cell count fall of 90%
or one opportunistic infectionc
8.76 7.92 920 65
Rate of CD4 cell count decline
 + 25% 8.43 7.54 910 74
 − 25% 9.51 8.61 920 79
Routine care costs
 + 50% 8.89 7.99 1040 78
 − 50% 8.89 7.99 950 75
CD4 cell count test costs
 + 50% 8.89 7.99 920 76
 − 50% 8.89 7.99 910 76
Discount rate
 5% 930 76
 0% 8.89 7.99 880 77

ART, antiretroviral therapy; CE, cost-effectiveness; PI, protease inhibitor; NNRTI, non-nucleoside reverse transcriptase inhibitor.

a

In all cases, the cost-effectiveness ratio of the sequence PI + 2NRTI → NNRTI + 2NRTI compared with co-trimoxazole alone is higher than the incremental cost-effectiveness ratio of the NNRTI + 2NRTI → PI + 2NRTI sequence compared with the PI + 2NRTI → NNRTI + 2NRTI. By accepted convention, when this occurs, the cost-effectiveness ratios are reported as ‘dominated’ [8,37]. Thus, the incremental cost-effectiveness ratio reported compares the NNRTI + 2NRTI → PI + 2NRTI sequence to no ART (co-trimoxazole alone).

b

Applying an incremental cost-effectiveness threshold criteria of three times the per capita gross domestic product for Côte d’Ivoire.

c

All strategies included co-trimoxazole prophylaxis starting at an observed CD4 cell count < 500/μl. Late-stage severe opportunistic infections included in the base case ART starting subset: severe fungal, isosporiasis, toxoplasmosis, non-tuberculosis mycobacterium, or other severe illnesses.