Table 1. Input parameters for model-based analyses.
Variable | Base Case Value | Range Examined | Reference |
Baseline cohort characteristics | |||
Undiagnosed HIV prevalence (%) | [10] | ||
Total | 0.4 | 0.1–1.0 | |
Age, mean years (SD) | 37 (14) | 27–47 | [10] |
Sex | [10] | ||
Male (%) | 35 | ||
Distribution of initial CD4, median cells/µl (IQR, SD) | |||
Chronic HIV infection* | 467 (606, 471) | [10] | |
Discount Rate (annual) | 3% | 0–3% | |
HIV RNA distribution in chronic HIV infection (%) | [15], [31] | ||
>100,000 copies/ml | 12.9 | ||
30,001–100,000 copies/ml | 12.9 | ||
10,001–30,000 copies/ml | 25.0 | ||
3,001–10,000 copies/ml | 25.2 | ||
501–3,000 copies/ml | 16.3 | ||
<500 copies/ml | 7.7 | ||
HIV testing protocols | |||
Average background HIV test frequency | Every 5 yrs | Every 3–7 yrs | [8] |
Sensitivity† (%) | 99.6 | [8], [32]–[35] | |
Specificity† (%) | 97.5 | [8], [32]–[35] | |
Provider strategy | |||
Test offer probability (%) | 36 | 30–100 | [10] |
Test acceptance probability (%)‡ | 75 | 30–100 | [10] |
Probability of HIV-detected to link to care (%) | 80 | 50–100 | [10] |
Counselor strategy | |||
Test offer probability (%) | 80 | 30–100 | [10] |
Test acceptance probability (%)‡ | 71 | 30–100 | [10] |
Probability of HIV-detected to link to care (%) | 80 | 50–100 | [10] |
Costs (2009 US$) | |||
Routine care (range by CD4, monthly) , off ART | 290–2,380 | [37]–[39] | |
Routine care (range by CD4, monthly), on ART | 240–1,080 | [37]–[39] | |
CD4 test | 70 | [40] | |
HIV RNA test | 120 | [40] | |
Acute OI events | [37]–[39] | ||
Pneumocystis jiroveci pneumonia | 13,120 | ||
Mycobacterium avian complex | 5,620 | ||
Toxoplasmosis | 31,320 | ||
Cytomegalovirus | 8,010 | ||
Fungal infections | 8,930 | ||
Other opportunistic infections | 6,010 | ||
Mortality (treated and untreated patients) | [37]–[39] | ||
Any OI event | 93,990 | ||
Chronic AIDS | 59,670 |
SD: Standard deviation; IQR: Inter-quartile range; OI: Opportunistic infection.
*Starting CD4 cell count, on average, for prevalent cases.
Sensitivity and specificity refer to the characteristics of a single rapid test, not the confirmatory process; test sensitivity is assumed to be 2.5% (the false positive rate) during the acute infection window period (approximately 2 months).
Probability of test acceptance is conditional upon being offered a test.