Drug and alcohol specimens are collected to help identify a patients drug or alcohol use.1 This information may be needed to obtain evidence for a possible criminal charges (such as after an accident), to help determine a cause of death, and to screen for employment suitability or adherence to an ongoing drug addiction rehabilitation program. Its also used to establish a differential diagnosis for a patient experiencing an altered mental state or who has signs and symptoms as slurred speech, dizziness, confusion, blurred vision, anxiety, hallucinations, memory impairment, lack of muscle coordination, or hyperthermia. The collection method and source of the specimens vary, based on the reason for testing. Because of the variability in local and state laws, each facilitys guidelines must be strictly followed.
Drug testing thats performed to determine employment suitability and rehabilitation program adherence usually involves a urine sample collected under highly controlled conditions.1 Although collection requirements may vary slightly, depending on the employer and type of employment or rehabilitation program, most include a designated collection site, security for the collection site, use of authorized personnel, privacy during collection, integrity and identity of the specimen, and chain-of-custody documentation. Some rehabilitation programs and employment circumstances may require the specimen collection to be observed. Testing is usually limited to five drug types: marijuana, cocaine, opiates, amphetamines, and phencyclidine (PCP). In the case of employment screening, if the results of the initial test are positive, a test using gas chromatographymass spectrometry follows to confirm the results.
Depending on the reason for collection and state laws, the patient or a family member may need to provide informed consent before you obtain the sample. Consent may not be required if its an emergency, if results will be used only for a differential diagnosis in an acute crisis, or if the patient is not in a condition to grant permission.2 In a criminal case, a law enforcement officer cant order blood to be drawn and doesnt have the legal right to grant permission if the patient refuses consent.
Blood specimens are collected in 10-mL gray-top blood collection tubes that contain a preservative (100 mg of sodium fluoride) to help prevent deterioration of the specimen, including changes in alcohol concentration and the breakdown of cocaine. The tubes also contain an anticoagulant (20 mg of potassium oxalate) to prevent the sample from clotting.3 The integrity and identity of the specimen must be maintained and, if indicated, chain-of-custody documentation preserved.
In general, prescription and over-the-counter drugs can be detected in blood within 4 to 24 hours and in urine for 2 to 4 days. Detection times for alcohol and other drugs vary. (See Drug detection times.)
This procedure focuses on drug and alcohol specimen collection for medicolegal reasons. When specimens are collected for a patient whos experiencing an altered mental state or other signs and symptoms, be sure to use the appropriate collection tubes. (See the "Venipuncture" procedure.)
Gloves chain of custody labels chain of custody form with multiple copies labels pen "limited access" signs Optional: vital signs monitoring equipment, pulse oximeter and probe, secure refrigerator.
Urine Specimen Collection
Urine collection container with temperature measurement device attached in sealed covering 90-mL plastic, screw-top specimen container in sealed covering adhesive label plastic sealable shipping bag absorbent material bluing agent for toilet water lockable cabinet or box
Blood Sample Collection
Two 10-mL gray-top Vacutainer blood tubes containing sodium fluoride and potassium oxalate with adhesive labels venipuncture supplies alcohol-free swab (povidone-iodine) evidence seals padded transport box laboratory biohazard transport bag Optional: 2" × 2" (5 cm × 5 cm) gauze pads, soap (non-alcohol containing) and water solution.
Note: Prepackaged blood and urine collection kits are commercially available and contain everything necessary to collect and preserve the chain of custody for the specimens.
Inspect all equipment and supplies. If a product is expired, is defective, or has compromised integrity, remove it from patient use, label it as expired or defective, and report the expiration or defect as directed by your facility. Make sure that access to collection materials and specimens is adequately restricted. Make sure that LIMITED ACCESS signs are posted in the specimen collection area to ensure patient privacy during the specimen collection process.
Urine Sample Collection
Blood Sample Collection
NURSING ALERT Complete all of the above steps in full view of the patient and, if applicable, the appropriate law enforcement officer.
If specimen collection is performed with no subsequent medical follow-up, serious medical conditions may go unidentified, causing the patient to experience adverse effects. Mishandling of the specimen or improper documentation of the chain of custody may lead to the evidence being inaccurate or inadmissible in court.
There are many ways for patients to circumvent testing: adding adulterants to urine at the time of testing, diluting urine through excessive water ingestion, consuming substances that interfere with testing, and substituting a clean urine sample. Appropriate collection techniques and tests of specimen integrity can reduce the risk of tampering.1
Record the date and time, what test was performed, the reason for the test, and the type of specimen that was obtained. Note whether a law enforcement officer was present for the specimen collection, including the agency the officer represented and the officers badge number. Document that the chain of custody was preserved. Document teaching provided to the patient and family (if applicable), their understanding of that teaching, and any need for follow-up teaching.
Ordering and interpretation
. American Family Physician, 99(1), 3339. https://www.aafp.org/afp/2019/0101/p33.html (Level VII)Patients rights. 42 C.F.R. § 482.13(b)(2)
.Accreditation requirements for acute care hospitals
. Chicago, IL: Accreditation Association for Hospitals and Health Systems. (Level VII)Recommendations of the Healthcare Infection Control Practices Advisory Committee and the HICPAC/SHEA/APIC/IDSA Hand Hygiene Task Force
. MMWR Recommendations and Reports, 51(RR-16), 145. https://www.cdc.gov/mmwr/pdf/rr/rr5116.pdf (Level II)Infection control. 42 C.F.R. § 482.42
.Accreditation requirements for acute care hospitals
. Chicago, IL: Accreditation Association for Hospitals and Health Systems. (Level VII)Patients rights. 42 C.F.R. § 482.13(c)(1)
.Accreditation requirements for acute care hospitals
. Chicago, IL: Accreditation Association for Hospitals and Health Systems. (Level VII)Accreditation requirements for acute care hospitals
. Chicago, IL: Accreditation Association for Hospitals and Health Systems. (Level VII)Medical record services. 42 C.F.R. § 482.24(b)
.Accreditation requirements for acute care hospitals
. Chicago, IL: Accreditation Association for Hospitals and Health Systems. (Level VII)