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Test ID: CDP
Chlordiazepoxide, Serum

Secondary ID A test code used for billing and in test definitions created prior to November 2011

8610

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

Monitoring chlordiazepoxide therapy  

 

Because chlordiazepoxide has a wide therapeutic index and dose-dependent toxicity, routine drug monitoring is not indicated in all patients

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

High-Performance Liquid Chromatography (HPLC)

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

Chlordiazepoxide, S

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

Benzodiazepines
Librium (Chlordiazepoxide)

Specimen Type Describes the specimen type needed for testing

Serum Red

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: Red top

Specimen Volume: 3 mL

Collection Instructions: Spin down within 2 hours of draw.

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.

1.1 mL

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

Hemolysis

Mild OK; Gross reject

Lipemia

Mild OK; Gross reject

Icterus

Mild OK; Gross reject

Other

Serum gel tube

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
Serum RedRefrigerated (preferred)14 days
 Ambient 14 days
 Frozen 14 days

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

Chlordiazepoxide (Librium) is a benzodiazepine widely used in the treatment of anxiety. It is also used in the treatment of alcohol withdrawal symptoms, as a premedication for anesthesia, in obstetrics during labor, as a muscle relaxant, and as an anticonvulsant. Toxic manifestations can include confusion, ataxia, sedation, tachycardia, hyperreflexia, and hypertension. Fatalities resulting from overdose are rare.

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.

Therapeutic concentration: 1.0-3.0 mcg/mL

Chronic use: 5.0-10.0 mcg/mL

Toxic concentration: > or =15.0 mcg/mL

 

The reference range cited (5.0-10.0 mcg/mL) relates to chronic therapy with chlordiazepoxide. Concentrations in the range of 1.0-3.0 mcg/mL are typical for occasional, non-chronic use. Concentrations as high as 80 mcg/mL may be observed in aggressive therapy with chlordiazepoxide for treatment of delirium tremens.

Interpretation Provides information to assist in interpretation of the test results

A therapeutic dose will yield a serum concentration of 1 to 3 mcg/mL.

 

In the treatment of delirium tremens, concentrations up to 10 mcg/mL are typical.

 

Toxic concentration: > or =15 mcg/mL.

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

No significant cautionary statements

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

1. Judd LL: The therapeutic use of psychotropic medications: antianxiety or anxiolytic medications. In Harrison's Principles of Internal Medicine. 12th edition. Edited by JD Wilson, E Braunwald, KJ Isselbacher, et al. New York, McGraw-Hill Book Company, 1991, pp 2143-2144

2. Scharf MB, Khosla N, Brocker N, Goff P: Differential amnestic properties of short- and long-acting benzodiazepines. J Clin Psychiatry 1984;45:51-53

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

Chlordiazepoxide is extracted from neutral serum into an organic phase that is then dried under nitrogen to concentrate the specimen. A small aliquot of the specimen is then analyzed by HPLC.

                                                             

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.

Thursday; 9:00 a.m.

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

7 days

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.

80154

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
8610Chlordiazepoxide, S3457-9