Table 1.
Parameters in the simulation
| Parameter in simulation | Value |
|---|---|
| Size of cohort | 2000 subjects |
| Duration of follow-up | 5 years |
| Proportion of subjects with CD4 <200 cells/ml | 30% |
| Proportion of subjects virologically suppressed | |
| CD4 <200 cells/ml | 50% |
| CD4 ⩾200 cells/ml | 80% |
| Probability of TMP-SMX prescription if CD4 <200 cells/ml | 80% |
| Probability of TMP-SMX adherence | |
| HIV viral load <1000 copies/ml | 100% |
| HIV viral load ⩾1000 copies/ml | 25% |
| Baseline risk of SSTI | 0·000125/day |
| Hazard ratio of SSTI* | |
| CD4 <200 cells/ml (immunological effect) | 3 |
| HIV viral load <1000 copies/ml | 0·5 |
| TMP-SMX use | 0·7 |
TMP-SMX, Trimethoprim-sulfamethoxazole; SSTI, skin and soft tissue infection.
This is the independent multiplicative increase in risk associated with each factor. That is to say, those with CD4 count <200 cell/ml experience a risk of SSTI which is triple that observed in subjects with a higher CD4 count, subjects with HIV viral load <1000 copies/ml experience a risk of SSTI which is half that seen in subjects with higher viral loads, and TMP-SMX users experience a risk of SSTI which is 0·7-fold that seen in subjects not using TMP-SMX.