4.7 Review

Correlation between oral fluid and blood THC concentration: A systematic review and discussion of policy implications

Journal

ACCIDENT ANALYSIS AND PREVENTION
Volume 173, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.aap.2022.106694

Keywords

Cannabis; Marijuana; THC; Oral fluid; Blood; Impaired driving

Funding

  1. National Public Health Institute (Helsinki, Finland) [SUB-B27020B-E3-S07.18222-2002, TREN-05-FP6TR-S07.61320-518404-DRUID]
  2. European Commission [SUB-B27020B-E3-S07.18222-2002, TREN-05-FP6TR-S07.61320-518404-DRUID]
  3. U.S National Highway Traffic Safety Administration (NHSTA)

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Cannabis is the second most commonly used impairing substance by drivers, and there is concern about the increase of cannabis-impaired driving as more countries legalize cannabis. However, the correlation between oral fluid THC and blood THC at the individual level is poor. Oral fluid THC testing as a biomarker for illegal THC concentrations in randomly selected drivers may result in a large number of false positive tests.
Cannabis is the second most commonly used impairing substance by drivers, after alcohol. As more countries legalize cannabis, there is concern that cannabis-impaired driving will increase. In many countries, police use roadside devices to test for oral fluid THC (the primary psychotropic component in cannabis) to identify drivers who used cannabis; including in countries with non-zero per se limits for THC in blood. This practice is questioned as previous research demonstrates a poor correlation between oral fluid and blood THC concentrations at the individual level. We conducted a meta-analysis to identify all research that compared oral fluid with blood THC levels. We obtained individual-level data from study authors and analyzed pooled individual-level data to calculate sensitivity and specificity of oral fluid THC (at various cut-off values) to detect blood THC above different concentration limits. Finally, we explored practical implications of using oral fluid THC in an enforcement context. Our review found THC concentrations measured in over 18,000 paired samples of oral fluid and blood. We found a good correlation between the presence of THC in oral fluid and presence of THC in blood (sensitivity = 71.2%, specificity = 97.7%). However oral fluid THC, at commonly used cut-off values, is less sensitive and less specific when used as a biomarker to detect people with blood THC concentrations above commonly used per se limits (such as 5 ng/mL). As such, there will be a large number of false positive tests if oral fluid THC testing were used as a biomarker for illegal THC concentrations in randomly selected drivers. We argue that the adverse implications of false positive oral fluid THC tests in this context outweigh the possible road safety benefits and we recommend against oral fluid THC screening in randomly selected drivers in countries with nonzero per se limits for blood THC. In contrast, oral fluid THC tests appear to be useful for investigating high-risk drivers who come to police attention because of evidence of impairment.

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