Drug Monitoring, Assess Panels, Quantitative, Urine
Test codes:
Clinical use
Clinical background
Drug testing in the clinical setting can provide information that improves patient care and prompts important clinical discussions with patients.1 For example, absence of an expected drug could suggest poor adherence or diversion, whereas detection of a nonprescribed licit or illicit drug could raise concerns regarding substance misuse.
Urine drug testing provides an objective assessment of drug use. Testing can be divided into presumptive and definitive tests. Presumptive drug tests (eg, immunoassays) are used to detect possible use of many drug classes at the point of care. However, they do not necessarily determine which drug a patient is taking.
Definitive drug tests use more complex methods (eg, liquid chromatography-tandem mass spectrometry [LC-MS/MS]) to identify specific drugs and metabolites in the test specimen. They can be used to confirm presumptive test results, or as an initial screen, but require specialty laboratory expertise. Quantitative tests indicate drug levels in the urine, whereas qualitative tests indicate the presence or absence of a given drug relative to established cut-off levels.
Panel testing that simultaneously measures a broad array of drug classes using definitive mass spectrometry–based testing is a means of establishing baseline drug use (prescription and non-prescription) in some patients. However, no single panel can be used to address all clinical needs; the availability of multiple testing options allows more flexibility for the physician.2
The Drug Monitoring, Assess Panels, Quantitative, Urine (test codes 39989, 39991, and 39992) provide options for assessing the presence of different drug classes, depending on clinical needs (Table 1). Panel components may be ordered separately. In addition, medMATCH® reports (test code 39158) can be ordered for these panels to match assay results to prescription information.
Table 1. Drugs (Individual Test Codes) Included in the Panels
Base panel (test code 39989) |
Plus panel (test code 39991) |
Extended panel (test code 39992) |
The American Society for Addiction Medicine (ASAM) has guidance on the clinical need to include various drugs in panel testing.3 Panels should be based on the patient’s drug(s) of choice, prescribed medications, and drugs commonly used in the patient’s geographical location and peer group.3
In general, the frequency of testing depends on the physician’s clinical judgment based on the patient’s diagnosis and reason for drug testing.2 For outpatients and partially hospitalized patients, ASAM recommends more frequent testing during the addiction stabilization period, tapering from methadone and buprenorphine, and the period thereafter; less frequent testing is indicated during the maintenance phase of treatment.3
The Centers for Disease Control and Prevention (CDC) recommends that clinicians consider the benefits and risks of drug testing before starting opioid treatment and at least annually during opioid treatment.4
Individuals suitable for testing
Method
Interpretive information
A "positive" result indicates that a drug or its metabolite has been definitively quantified at or above its cut-off value. A "negative" result indicates that a drug or its metabolite was not present at levels above the cut-off value.
medMATCH reports, if ordered, indicate whether a detected drug was prescribed ("consistent") or not prescribed ("inconsistent") or whether a prescribed drug was not detected ("inconsistent"). The latter result may indicate noncompliance with the treatment plan or diversion.
Quantitative values indicate drug and/or metabolite levels in the urine specimen but cannot be used to assess the drug dose because excreted drugs are extensively metabolized; many factors, including genetics, age, weight, health conditions, and other medications, may influence how the body processes drugs.
Urine specimen validity results indicating a pH outside the 4.5 to 9.0 range, creatinine <20 mg/dL with abnormal specific gravity, and/or presence of oxidants ≥200 μg/mL are considered to render the drug testing results invalid because of suspected adulteration, dilution, or both.2
These panels are not designed to determine clinical impairment. For example, assessment of clinical impairment due to opioid misuse should be based on behavior, cognitive function, motor performance, and somnolence, independent of the presence of an opioid or its metabolite.5
No single monitoring approach provides adequate information about the pattern or dose of patient drug use. Safest prescribing habits should include a combination of tools and laboratory test results to correctly detect drug use patterns.
References
Content reviewed 9/2025
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
The tests listed by specialty and category are a select group of tests offered. For a complete list of Quest Diagnostics tests, please adjust the filter options chosen, or refer to our Directory of Services.