From: Management of pharmaceutical and recreational drug poisoning
Toxicological screening methods | Comments–interpretation | ||
---|---|---|---|
Rapid screening methods on an automated chemistry analyzer | Immunological and enzymatic | Urine screens for illicit drugs and/or their metabolites (cocaine, amphetamines, opiates, etc.) without assay | Useful for “conventional” drugs, excluding NPS |
These tests need to be carefully interpreted (molecule identified by antibody, toxicokinetics, screening window, interferences, etc.) | |||
Limits of interpretation on urine | |||
Specific drug or toxin screens with blood and/or urine assays | Useful for blood assays (drugs, ethanol, etc.) | ||
Limits of interpretation on urine | |||
Drug class screens (benzodiazepines, tricyclic antidepressants, etc.) in blood and/or urine | Limits of interpretation for a drug of the class identified by antibody due to cross-reactions with other drugs of the same class and possible interferences | ||
Need for biological interpretation with respect to the toxicity thresholds of each drug | |||
Limits of interpretation for urine | |||
Chromatographic confirmation of screening methods | Liquid or gas chromatography | Detection by diode arrays and/or mass spectrometry in blood and/or urine | Useful for broader targeted screening (up to 1200 molecules and/or metabolites) |
Need for biological interpretation of the nature of the molecules identified, the level of screening (sensitivity) and interpretation with respect to reported toxic concentrations | |||
A semiquantitative approach can be used simultaneously with screening for certain molecules | |||
Limits of interpretation on urine | |||
Liquid chromatography | High-resolution mass spectrometry (HRMS) | Useful to identify unknown chemical structures (non-targeted screening) (e.g. NPS) |