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Mayo Test ID ALC Ethanol, Blood


Ordering Guidance


This test is not performed using chain of custody. For chain of custody testing order ALCX / Ethanol, Chain-of-Custody, Blood.



Specimen Required


Container/Tube:

Preferred: Gray top (potassium oxalate/sodium fluoride)

Acceptable: Lavender top (EDTA) or green top (sodium heparin)

Specimen Volume: 2 mL

Collection Instructions:

1. Do not use alcohol to clean arm. Use an alternative, such as Betadine, to cleanse arm before collecting any specimen for volatile testing.

2. Specimen must be sent in original tube. Do not aliquot.


Useful For

Detection of ethanol (ethyl alcohol) in blood to document prior consumption or administration of ethanol

 

Quantification of the concentration of ethanol in blood correlates directly with degree of intoxication

 

This test is not intended for use in employment-related testing.

Method Name

Headspace Gas Chromatography with Flame Ionization Detector (HSGC-FID)

Reporting Name

Ethanol, B

Specimen Type

Whole Blood NaFl-KOx

Specimen Minimum Volume

0.5 mL or amount to fill 1 tube

Specimen Stability Information

Specimen Type Temperature Time Special Container
Whole Blood NaFl-KOx Refrigerated (preferred) 14 days
  Frozen  28 days
  Ambient  24 hours

Reject Due To

Gross lipemia Reject
Gross icterus OK

Clinical Information

Ethanol is one of the most widely abused legal substances in the United States. It is the active agent in beer, wine, vodka, whiskey, rum, and other liquors.

 

Ethanol acts on cerebral functions as a depressant similar to general anesthetics. This depression causes most of the typical symptoms such as impaired thought, clouded judgment, and changed behavior. As the level of alcohol increases, the degree of impairment becomes progressively increased.

 

In most jurisdictions in the United States, the level of prima facie evidence of being under the influence of alcohol for purposes of driving a motor vehicle is 80 mg/dL (0.08% in whole blood).

Reference Values

Not detected (Positive results are quantified.)

Limit of detection: 10 mg/dL (0.01 g/dL)

Legal limit of intoxication is 80 mg/dL (0.08 g/dL).

Toxic concentration is dependent upon individual usage history.

Potentially lethal concentration: ≥400 mg/dL (0.4 g/dL)

Interpretation

The presence of ethanol in blood at concentrations above 30 mg/dL (>0.03% or g/dL) is generally accepted as a strong indicator of the use of an alcohol-containing beverage.

 

Blood ethanol levels above 50 mg/dL (>0.05%) are frequently associated with a state of increased euphoria.

 

Blood ethanol level above 80 mg/dL (>0.08%) exceeds Minnesota's legal limit for driving a motor vehicle. These levels are frequently associated with loss of manual dexterity and with sedation.

 

A blood alcohol level of 400 mg/dL (≥0.4%) or higher may be lethal as normal respiration may be depressed below the level necessary to maintain life.

 

The blood ethanol level is also useful in diagnosis of alcoholism. A patient who chronically consumes ethanol will develop a tolerance to the drug and requires higher levels than described above to achieve various states of intoxication. An individual who can function in a relatively normal manner with a blood ethanol level above 150 mg/dL (>0.15%) is highly likely to have developed a tolerance to the drug achieved by high levels of chronic intake.

Cautions

Whole blood is required (not serum or plasma).

Clinical Reference

Langman LJ, Bechtel LK, Holstege CP. Clinical toxicology. In: Rifai N, Chiu RWK, Young I, Burnham CAD, Wittwer CT, eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier; 2023:454

Method Description

Specimens are analyzed and quantitated using headspace gas chromatography with flame ionization detection.(Baselt RC. Disposition of Toxic Drugs and Chemicals in Man. 10th ed. Biomedical Publications; 2014:2211)

Day(s) Performed

Monday through Saturday

Report Available

1 to 2 days

Specimen Retention Time

2 weeks

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

80320

G0480 (if appropriate)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
ALC Ethanol, B 56478-1

 

Result ID Test Result Name Result LOINC Value
30908 Ethanol, B 56478-1