Required section · Section 4 of 6
Guided case: resolve the opiate screen
An outpatient pain-management urine specimen collected at a scheduled visit has an opiate immunoassay positive using a local 300 ng/mL morphine-equivalent cutoff, not a forensic collection. The patient reports hydrocodone/acetaminophen twice daily, with the last dose about 14 hours before collection.
Reflex LC-MS/MS reports hydrocodone 850 ng/mL, norhydrocodone 210 ng/mL, and hydromorphone 40 ng/mL. Hydrocodone identification requires a quantifier transition, qualifier transition with accepted ion ratio, retention-time match, and stable-isotope internal standard; a single peak at one retention time is not definitive identification.
Norhydrocodone with hydrocodone is consistent with hydrocodone metabolism, and the small hydromorphone concentration can be a minor metabolic finding. Absence of 6-monoacetylmorphine argues against recent heroin exposure within that analyte's detection window, but its short window prevents a broader exclusion. The definitive pattern supports language such as consistent with prescribed hydrocodone therapy.
Urine creatinine is 62 mg/dL and specific gravity is 1.018. These values do not meet the federal dilute or substituted criteria stated in the table. They do not turn urine concentrations into a dose measurement.
Use a metabolite pattern to explain a result, then stop at the boundary of what that pattern supports. Compare the pattern with the method limits. Do not convert it into an adherence clock.
Illustrative drawing — this picture was drawn rather than captured.
| Test or measure | Result | Method or criterion | Interpretive use |
|---|---|---|---|
| Opiate screen | Positive | Immunoassay, local cutoff 300 ng/mL morphine-equivalent | Presumptive class signal |
| Hydrocodone | 850 ng/mL | LC-MS/MS | Definitive target analyte |
| Norhydrocodone | 210 ng/mL | LC-MS/MS | Consistent metabolic marker |
| Hydromorphone | 40 ng/mL | LC-MS/MS | May be minor hydrocodone metabolite |
| 6-monoacetylmorphine | Not detected | LC-MS/MS, detection limit 2 ng/mL | No evidence at this window |
| Creatinine / specific gravity | 62 mg/dL / 1.018 | Specimen validity measures | Does not meet federal dilute or substituted criteria |
| Hydrocodone identification evidence | Quantifier/qualifier transitions, accepted ion ratio, retention-time match, stable-isotope internal standard | Validated LC-MS/MS | Combined transitions, accepted ion ratio, retention-time match, and stable-isotope internal standard support definitive identification. |
| Classification | Creatinine | Specific gravity |
|---|---|---|
| Dilute | at least 2 and less than 20 mg/dL | greater than 1.0010 and less than 1.0030 |
| Substituted | less than 2 mg/dL | at most 1.0010 or at least 1.0200 |
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