I'll set the stage with what I consider my well researched knowledge of PEth testing. I'm not defending the test, just summarizing what I've learned from a multitude of research papers and my own personal experience.
The test is looking for the presence of a phospholipid in the red blood cycles called Phosphatidyl ethanol (PEth). PEth is formed when an enzyme (PLD) does it's work in the presence of ethanol. Normally PLD utilizes water, but ethanol is more chemically available/active for the reactions performed by PLD and thus the products are modified in solutions containing ethanol.
Unless one can figure out a way to make a significant number of clean red blood cells (which would have it's own medical consequences) there is no "cheating the system". PEth is effectively sequestered in the cell membrane of RBCs until they die and are recycled, or PEth naturally degrades and is removed from the blood.
There are a few isomers of PEth, with the most common one used for testing being PEth 16:0/18:1 (numbers have to do with bond locations and carbon chain lengths in the molecule). Most intravenous testing is using liquid chromatography with tandem mass spectrometry for analysis. A highly sensitive and accurate methodology with a level of detection and quantification well below the cutoffs.
The typical cutoff for a PEth test is 20ng/ml in the U.S. Being above this cutoff indicates "moderate to heavy drinking". Overseas the cutoffs vary and are much higher. It's not uncommon to see cutoffs in the 200 ng/ml range being considered as "excessive drinking". There is not a lot of consensus that the detected level can be used to quantitatively measure the consumption of alcohol due to differences in PEth production and metabolism varying between individuals. The test is intended to qualitatively measure drinking and most specifically detect binge drinking (1-2 isolated heavy drinking sessions) or long term low level consumption of alcohol (1-2 beers per day across weeks).
The general forensic consensus is that a substance is detectable for 5 half lives in the human body. Most research is showing PEth with approximately a 4-5 day half life. This varies by subject, and there does seem to be evidence that half life is effected by the subject's history of drinking. Given this half life, the standard lookback window for the test is accepted to be a maximum of 28 days.
My opinion is that a test administered 2-5 days after a night out of heavy drinking has a high probability of resulting higher than the 20ng/ml cutoff.
Those interpreting the results are admonished that the test is not the end all be all, but should be used as a data point in the overall clinical and behavioral picture of the subject. Of course, many still view the test as the gold standard single point needed to detect undesired alcohol consumption. Additionally, PEth test are considered "laboratory developed tests" and are not "approved" by the FDA. They do not require the FDA to review trials data or research data before being marketed to the public.
The most common methods of testing are intravenous blood draw, or dried blood spot collection. It is possible to test hair or fingernails for PEth, but testing these mediums are much less common and there is little consensus of cutoffs.
Dried blood spot collection is (as demonstrated here) controversial and many believe the test to be prone to false positives. It appears DBS testing was developed by a company (USDTL) with a long history or marketing substance abuse testing. The protocol for DBS collection is fairly specific, and is not always performed by someone with adequate training. Furthermore, the post collection handling of collected samples can vary wildly as they are returned to the lab for analysis.
A little searching will pull up quite a few people that are not happy with USDTL for one reason or another. Those interested can research USDTL and draw their own conclusions.
I have read research that indicated PEth can form in blood samples outside the body (in vitro) if the sample contains ethanol. Were a sample to be collected from someone with alcohol in their system, or were that sample to be contaminated with ethanol it's feasible that elevated PEth levels would result. Remember, bacteria and fungus form alcohol during their normal metabolic proccess. It's not too far of a stretch to think a DBS sample could encounter alcohol producing bacteria or yeasts post or pre collection.
On the intravenous side, it would be highly inadvisable to allow the collecting phlebotomist to use an ETHYL alcohol swab prior to sticking you with the needle. I have not read anything that indicates other alcohols (isopropyl etc) could be an issue, but I would request an alternative sterilization technique just to be safe. Most practitioners should be happy to accommodate the request with iodine or some other agent.
Ironically, one study found that alcoholic's samples were more sensitive to this in vitro phenomenon.
My opinion is PEth testing is a pretty effective tool in assessing a subject's abstinence. The long lookback and high sensitivity make it very difficult for a substance abuser to game the system by timing tests. It also offers those in recovery a tool to prove compliance when some other much less reliable test produces a false positive (think ETG). If requested to take a dried blood spot PEth test I would refuse and offer to take the intravenous test. If I were "forced" to take a DBS, my next stop would for an intravenous one as backup. I'll take my chance with a medical laboratory over the method of administration for the DBS.
Thanks for the response, I am aware of what these tests are looking at, my question is in the regards of the legitimacy/false positives. A case for a possible false positive would be a Peth test taken via dried blood spot being positive and an intravenous 14 days later showing negative.
Assuming the dried blood spot was accurate, this would be a normal result. The additional 14 days provides the donor with 3 more half lives of time before the intravenous test. I would be even more suspicious if the DBS test quantified the PEth level near the 150 ng/ml range as this would give the normal metabolic processes in most donors time to drop the PEth level below the 20ng/ml cutoff.
Also a nail ETG test 25 days later (with a look back window of 90 days) being negative as well.
Nail ETG has a well documented high false negative rate. I've seen plenty of studies that put it around 70% accurate in catching someone drinking at best. Most of that 70% are those that are either drinking consistently or binging repeatedly during the lookback window. There's a delay between consumption of alcohol and ETG making it into the nail matrix. Some place this delay at up to 3 weeks, some claim it's much sooner. Either way it's not instant. There's also still quite a bit of controversy over just what the nail cutoffs should be for various substances.
There have also been documented cases of Peth tests taken the same day as coming back negative and positive. Was curious if any AME’s/lab techs that have heard of cases throughout the community or heard anything informal from the FAA about the test.
That would definitely indicate a problem with the testing. Assuming different samples (DBS and whole blood), different labs, and the same cutoff values I would accept the whole blood intravenous test as the more accurate result in this case.