Table 1.
Epidemiological Data Point |
Value, Rio de Janeiro (age 15–59) |
Model Output |
Matched Model Parameter | Parameter Value (Fit to Data) |
Sensitivity Analysis Range |
Reference |
---|---|---|---|---|---|---|
TB incidence, per 100,000/yr |
122 | 122 | Number of TB transmissions per infectious person-year |
6.54 | 5.13–7.50 | City of Rio de Janeiro27 |
TB prevalence, per 100,000 |
132 | 132 | Rate of TB diagnosis and treatment |
0.87/year | 0.78–1.00 | World Health Organization28 |
TB mortality, per 100,000/yr |
6.5 | 6.5 | Pre-diagnosis TB mortality rate (HIV-negative) |
0.038/year | 0.023–0.054 | City of Rio de Janeiro20 |
TB incidence in PLHIV, per 100,000 pop/yr |
15.7 | 15.7 | Proportion of new TB infections resulting in rapid progression (HIV-positive) |
1.0a | 0.09–1.0 | City of Rio de Janeiro20 |
Rate of slow TB progression after remote infection (HIV-positive) |
0.10/yeara | 0.04–0.31 | Gilks et al29 Horsburgh et al30 |
|||
TB mortality in PLHIV, per 100,000/yr |
1.54 | 1.54 | Pre-diagnosis TB mortality rate (HIV, CD4 ≤350) |
0.087/yearb | 0.048–0.130 | City of Rio de Janeiro20 |
ART coverage, CD4 ≤350 |
80% | 80.0% | Rate of ART initiation | 1.04/year | 0.77–1.47 | UNAIDS31 |
Rate of ART discontinuation | 0.2/year | 0.12–0.29 | Assumption | |||
HIV prevalence, per 100,000 |
600 | 600 | HIV incidence | 3.8x10−4/year | 1.7–5.9x10−4 | City of Rio de Janeiro20 |
HIV mortality, per 100,000/yr |
24.6 | 24.6 | HIV mortality rate (CD4 ≤350, non-TB) |
0.061/yearb | 0.030–0.100 | City of Rio de Janeiro20 |
Proportion of retreatment cases |
0.274 | 0.274 | TB relapse rate | 0.013/year | 0.006–0.030 | City of Rio de Janeiro20 |
Proportion of TB that is MDR |
0.019 | 0.019 | Relative infectiousness of MDR-TB |
0.65 | 0.33–0.85 | World Health Organization28 |
Proportion of MDR-TB that is retreatment |
0.52 | 0.52 | Proportion of recoveries ending in new MDR-TB |
0.005 | 0.002–0.007 | World Health Organization28 |
Literature-Based Model Parameter |
Value (from Literature) |
Sensitivity Range |
Reference | |||
Relative infectiousness of TB in PLHIV, per person-day |
0.75 | 0.4–1.0 | Golub et al32 | |||
Partial immunity to TB re- infection if latently infected |
0.56 | 0.0–1.0 | Cohen et al23 Sutherland et al33 Vynnycky et al34 |
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Proportion of infections that progress rapidly to active TB |
0.087 | 0.066–0.100 | Vynnycky et al34 | |||
Rate of slow progression from remote TB infection (HIV-negative) |
0.0005/year | 0.0002–0.0011 | Horsburgh et al30 | |||
Protective efficacy of IPT against reactivation TBc |
0.67 | 0.5–1.0 | Ferebee3 Akolo et al5 |
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Rate of CD4 progression to ≤350 cells/mm3 |
0.2 | 0.0–0.4 | Sanders et al35 | |||
Non-HIV, non-TB mortality | 0.004/year | 0.0–0.008 | City of Rio de Janeiro20 |
Initial estimates were that 25% of TB infections would result in rapid progression, and the rate of slow progression after remote infection was 0.026/year.30 However, these estimates resulted in substantial underestimates of the burden of HIV/TB. Reasoning that this was more likely due to underestimation of recent, rather than remote, infection (e.g., clustering of recent infection), we allowed the ratio between these two parameters to remain constant, even though this ultimately resulted in an estimated proportion of rapid TB progression equal to 1.0. This provides a maximally conservative estimate of the impact of IPT, which has no benefit against reinfection TB in the model. We also performed sensitivity analysis around a protective effect of antiretroviral therapy (ART) against TB infection of 0.0–1.0.
We assumed that HIV-infected populations with either CD4 nadir >350 cells/mm3 or use of ART would experience mortality rates at the mean of the rates listed for HIV-infected (CD4 ≤350) and -uninfected populations in the Table.
IPT was assumed to have a duration of effect of at least five years (the duration of the analysis); in a sensitivity analysis, this duration of effect was reduced to six months, as described in the text.