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. 2016 May 4;144(13):2889–2898. doi: 10.1017/S0950268816000789

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.