Background: Rapid tests offer the advantage of providing immediate test results to improve the effectiveness of follow-ups.
Objectives: We compare syphilis rapid tests with the standard (i.e., RPR/TP-PA) for screening MSM in an outreach program in the US.
Methods: We estimated the number of “successful referrals” for treatment (i.e., identified infected individuals who eventually present for treatment) and the total costs for three screening strategies: treponemal and nontreponemal dual antigen POC (Dual-POC, $11), Treponemal POC (TrepOnly-POC, $10) and the RPR($7)/TP-PA($22) (includes, test kits and labor cost). Treatment cost was not included. Assumptions: perfect performance for RPR/TP-PA (i.e., 100% sensitivity and specificity); individuals have perfect memory of their syphilis history; for the Dual-POC, nontrep-trep+ were retested with EIA if they had no history (conclude previous infection otherwise); if nontrep+trep+ or only trep+ and have had syphilis before, draw blood for quantitative RPR. Probabilities of presenting for treatment, no test results, 80%; if initial results provided (i.e., nontrep+/-trep+ or only trep+), 90% for repeat infections and 95% for new infections.
Results: For 10,000 individuals (1% infected and 10% previously infected), we estimated 10,000 blood-draws for RPR/TP-PA; 10,000 fingersticks for both POCs; 960 blood-draws for TrepOnly-POC; 295 blood-draws for Dual-POC. The final results: TrepOnly-POC – successful referrals 91, total cost $114,000, cost-effectiveness ratio (CE) $1,253; Dual-POC – successful referrals 91, total cost $116,000, CE $1,274; RPR/TP-PA – successful referrals 80, total cost $164,000, CE $2,050. The TrepOnly-POC strategy required drawing blood unnecessarily from a substantially higher number of individuals than the Dual-POC strategy (950 vs. 285). The Dual-POC was more cost-effective than the TrepOnly-POC ($1,274 vs $1,363) when the costs were the same ($11).
Conclusions: The Dual-POC test offers the additional advantage of eliminating unnecessary follow-ups for nontrep-trep+ individuals with previous infections.
Implications for Programs, Policy, and Research: Excluding information provided by the nontreponemal tests may result in unnecessary blood-draws/follow-ups.