Drugs of Abuse Panel, Meconium - Screen with Reflex to Confirmation/Quantitation
Preferred meconium test to detect and document maternal drug use during pregnancy approximately the last trimester of a full-term birth. Targeted single-drug class testing is appropriate if only a particular drug class or classes are of clinical interest, or when quantity of meconium available for testing is very small (eg <1g).
Qualitative Enzyme-Linked Immunosorbent Assay/Quantitative Liquid Chromatography-Tandem Mass Spectrometry
Meconium. All meconium (blackish material) excreted until milk/formula based stool (yellow-green) appears.
Transport all available meconium (4 g is preferred). (Min: 2 g or 3/4 inch cube on each side)
Ambient: 1 week; Refrigerated: 3 months; Frozen: 1 year
|Drugs Covered and Cutoff Concentrations|
|Amphetamines||30 ng/g||20 ng/g|
|Barbiturates||75 ng/g||50 ng/g|
|Benzodiazepines||75 ng/g||20 ng/g|
|Buprenorphine||40 ng/g||20 ng/g|
|Cocaine||30 ng/g||20 ng/g|
|Marijuana||30 ng/g||5 ng/g|
|Methadone||40 ng/g||10 ng/g|
|Opiates||30 ng/g||20 ng/g|
|Phencyclidine||15 ng/g||10 ng/g|
Meconium begins to form between the 12th and 16th week of gestation. Meconium drug testing can detect maternal drug use during the last 4 to 5 months of pregnancy. A negative result does not exclude the possibility that a mother used drugs during pregnancy. Detection of drug use depends on the quantity and quality of the specimen tested as well as the pattern and frequency of drug(s) used by the mother. Although not likely, drugs administered during labor and delivery may be detected in meconium. Interpretive questions should be directed to the laboratory.
The concentration at which the screening test can detect a drug or metabolite varies within a drug class. The concentration value must be greater than or equal to the cutoff to be reported as positive.
For medical purposes only; not valid for forensic use.
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
If the specimen screens positive, then Confirmation/Quantitation by LC-MS/MS will be added. Additional charges apply.
Unless ARUP is otherwise notified, reflex confirmation testing will be performed in the following order of priority:
Amphetamines (0.125 g sample required)
Cocaine (0.25 g sample required)
Opiates (0.125 g required)
Buprenorphine (0.125 g required)
Marijuana (0.125 g required)
Benzodiazepines (0.125 g sample required)
Methadone (0.125 g sample required)
Phencyclidine - PCP (0.25 g sample required)
Barbiturates (0.25 g sample required)
80307; if reflexed, add 80324; 80345; 80346; 80348; 80349; 80353; 80358; 80359; 80361; 80365; 83992 (Reflexed Alt Code: G0480 )
|Component Test Code*||Component Chart Name||LOINC|
- Pain Management