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VA/DoD CLINICAL PRACTICE GUIDELINE FOR OPIOID THERAPY FOR CHRONIC PAIN

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<strong>VA</strong>/<strong>DoD</strong> Clinical Practice Guideline for Opioid Therapy for Chronic Pain<br />

Appendix B: Urine Drug Testing<br />

A. Benefits of Urine Drug Testing<br />

Substance misuse in patients on LOT is more than 30% in some series.[107] The inaccuracies inherent to<br />

patient self-report coupled with the evident mortality and morbidity to the treated patients, their families,<br />

and others require additional methods to ascertain patient and public safety. UDT and confirmatory<br />

testing is an additional method of examining for patient substance misuse and adherence to the<br />

prescribed regimen as well as the development of trust within the provider-family-patient relationship. It is<br />

critical that the UDT and confirmatory testing be done in a timely, confidential, accurate, and easily<br />

available manner to assure the prescribers, patients, and public that safety, fairness, and trust are being<br />

addressed.<br />

Within the <strong>VA</strong>, verbal informed consent is required prior to UDT. While a patient can decline to consent to<br />

UDT, a provider can factor that declination into their thinking about whether it is safe to continue with OT<br />

for that patient which is ultimately required if LOT is to be instituted/continued. For more information, see<br />

the <strong>VA</strong> National Center for Ethics in Health Care website (http://www.ethics.va.gov/).<br />

B. Types of Urine Drug Testing<br />

There are three main types of UDT currently being utilized in clinical settings: immunoassay, GCMS<br />

confirmatory testing, and liquid chromatography-mass spectrometry (LCMS) confirmatory testing.<br />

Immunoassay screening is inexpensive, fast and widely available. However, there are a number of<br />

drawbacks for using this test alone. There is a higher potential for false positives and negatives as well as<br />

lack of specificity of the actual opiate or benzodiazepine being tested. GCMS is highly sensitive and<br />

specific; however, it is expensive and time consuming. LCMS is less expensive than GCMS but more<br />

expensive than immunoassay. It can give a confirmation for a large number of medications, substances<br />

and drugs at one time and may be helpful in many patients at initiation of OT, periodically during OT, and<br />

following cessation of OT if SUD is a possibility. See Table B-1 through Table B-4 and Figure B-1 for more<br />

information.<br />

Table B-1. Urine Toxicology Specimen Validity and Normal Characteristics of a Urine Sample<br />

[189-191]<br />

Urine Toxicology Specimen Validity<br />

Normal Characteristics of a Urine Sample<br />

• Urine samples that are adulterated, substituted, or Temperature within 4 minutes of voiding: 90-100⁰F<br />

diluted may avoid detection of drug use<br />

pH: 4.5-8.0<br />

• Urine collected in the early morning is most<br />

concentrated and most reliable<br />

Creatinine: >20 mg/dL<br />

• Excessive water intake and diuretic use can lead to<br />

Specific gravity: >1.003<br />

diluted urine samples (creatinine

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