Table 1.
N. gonorrhoeae | C. trachomatis | M. genitalium | T. pallidum | HIV | |
---|---|---|---|---|---|
Are host-pathogen interactions amenable to screening? | |||||
1. Undetected infection typically associated with serious adverse clinical outcomes | + | + | − | +++ | +++++ |
2. Long period between infection and disease onset | − | − | − | ++ | +++ |
3. Not spontaneously cleared by immune system | − | − | − | +++ | +++++ |
4. Natural immunity from recovered infection | +++ | + | +++ | + | ++++ |
High risk of inducing AMR? | |||||
1. High risk of inducing AMR in pathogen itself given standard therapy | ++++ | + | ++++ | + | − |
2. High risk of inducing AMR in microbiome given standard therapy | +++ | ++ | +++ | + |
Example 1. For the first criterion, there is little or no evidence that MG is associated with serious adverse clinical outcomes and MG is thus scored ‘−’, whereas there is plenty of evidence that HIV is associated with severe outcomes and HIV is thus scored ‘+++++’.
Example 2. In the case of HIV for the fourth criterion, an HIV infection is not eradicated by the immune system and thus there is no immunity. HIV thus gets a favourable score for being amenable to screening on this criterion.
This scoring is not based on a systematic review but on a subjective assessment of the authors’ evaluation of the scientific literature. Each infection is rated from ‘−’ to ‘+++++’ according to the evidence base underpinning the criterion and the clinical significance.