http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6005a1.htm?s_cid=mm6005a1_wI have been a medical technologist since 1974. When I learned to perform basic syphilis serologies we did the RPR test. If this was positive, a test called FTA-ABS was done to confirm the positive, as RPR's do have some cross-reactivity with other disease states. This fact has been known for a long time. The other test that was performed for syphilis testing is the VDRL. This is a manual test that requires a bit more finesse in performance than an RPR. I can remember performing 50+ RPR's per day, as back then, we did them on all new admits. We kept track of the positives. Follow-up testing with the FTA-ABS test was not done that often.
This testing issue is much more complex than what is stated in the lead article. Labs are looking for methods that are automated and accurate that can be performed on hundreds of specimens per day (in the case of large reference laboratories). This article is about methodology, not lab error.
I am familiar with some of the terminology in the article cited above, but I will admit that I would have to sit down and really study it before I understand it. If you have no medical or lab background, I guarantee you will have problems understanding the jargon and the issues.
Please do NOT assume that it is always the lab's fault. It is a very regulated industry. We perform controls on testing that requires them and inspectors always look at QC logs first. Labs are inspected by JCAHO, CAP, State health departments and other entities, depending on what type of lab it is and what testing is performed there.