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Test ID: VLTB
Volatile Screen, Blood

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Useful For Suggests clinical disorders or settings where the test may be helpful

Detection and quantitation of acetone, methanol, isopropanol, and ethanol in whole blood

 

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

 

Evaluation of toxicity to the measured volatile substances

Method Name A short description of the method used to perform the test

Headspace Gas Chromatography-Flame Ionization Detector (HSGC-FID)
Includes methanol, ethanol, isopropanol, and acetone.

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Volatile Scrn, B

Aliases Lists additional common names for a test, as an aid in searching

Acetone
Alcohol
Ethanol
Ethyl Alcohol
ETOH (Ethanol)
Isopropanol
Methanol

Specimen Type Describes the specimen type needed for testing

Whole blood

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

Container/Tube: 

Preferred: Grey top (potassium oxalate/sodium fluoride)

Acceptable: Any anticoagulant

Specimen Volume: 1 mL

Collection Instructions: Do not use alcohol to clean arm. Use alternative such as Betadine to cleanse arm before collecting any specimen for volatile testing.

Additional Information: Ethylene glycol requires a separate request. See ETGL/8749 Ethylene Glycol, Serum.

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

0.5 mL or amount to fill 1 tube

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis

Mild OK; Gross OK

Lipemia

Mild OK; Gross OK

Icterus

Mild OK; Gross OK

Other

NA

 

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
Whole bloodRefrigerated (preferred)72 hours
 Frozen 14 days
 Ambient 24 hours

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Volatile substances in the blood include ethanol, methanol, isopropanol, and acetone. Acetone is generally elevated in metabolic conditions such as diabetic ketoacidosis. Methanol and isopropanol are highly toxic and result from exogenous ingestion.

 

Ethanol is the single most important substance of abuse in the United States. It is the active agent in beer, wine, vodka, whiskey, rum, and other liquors. Ethanol acts on cerebral function 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 progressively increases.

 

In most jurisdictions in the United States, the per se blood level for being under the influence of alcohol (ethanol) for purposes of driving a motor vehicle is 80 mg/dL.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

METHANOL

Not detected (Positive results are quantitated.)

Toxic concentration: > or =10 mg/dL

 

ETHANOL

Not detected (Positive results are quantitated.)

Toxic concentration: > or =400 mg/dL

 

ISOPROPANOL

Not detected (Positive results are quantitated.)

Toxic concentration: > or =10 mg/dL

 

ACETONE

Not detected (Positive results are quantitated.)

Toxic concentration: > or =10 mg/dL

Interpretation Provides information to assist in interpretation of the test results

Toxic concentrations:

-Methanol: > or =10 mg/dL

-Ethanol: > or =400 mg/dL

-Isopropanol: > or =10 mg/dL

-Acetone: > or =10 mg/dL

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

This test does not detect ethylene glycol.

Clinical Reference Provides recommendations for further in-depth reading of a clinical nature

1. Caplan YH: In Forensic Science Handbook. Vol. 1. Edited by R Saferstein. Englewood Cliffs, Prentice Hall, 1982

2. Goodman and Gilman's: The Pharmacological Basis of Therapeutics. Seventh edition. Edited by TW Rall, F Murad. New York, McMillan Publishing, 1985

3. Porter WF, Moyer TP: Clinical toxicology. In Tietz Textbook of Clinical Chemistry. Fourth edition. Edited by CA Burtis, ER Ashwood. Philadelphia, WB Saunders Company, 1993, pp 1155-1235

4. Principles of Forensic Toxicology. Edited by B Levine. Washington DC, American Association of Clinical Chemistry, 1999

Method Description Describes how the test is performed and provides a method-specific reference

Specimens are analyzed and quantitated by headspace gas chromatography-flame ionization detection.(Sunshine I: Methodology for Analytical Toxicology. Cleveland, OH, CRC Press, 1975, p 145)

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Monday through Sunday; Varies

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

Same day/1 day

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

1 day

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

14 days

Performing Laboratory Location The location of the laboratory that performs the test

Rochester

Test Classification Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.

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

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

84600-Screen

82010-Acetone (if appropriate)

82055-Ethanol (if appropriate)

82491-Isopropanol (if appropriate)

82491-Methanol (if appropriate)

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
89190Volatile Scrn, B41266-8
30921Methanol, B9334-4
30922Ethanol, B5640-8
30923Acetone, B9425-0
30924Isopropanol, B5667-1
34377Chain of CustodyN/A