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Test ID HYPOG Hypoglycemic Agent Screen, Serum

Useful For

Evaluation of suspected insulinoma characterized by hypoglycemia and increased plasma insulin concentration.

 

Detecting drugs that stimulate insulin secretion

 

If hypoglycemia is the result of 1 of these drugs, the test will detect the drug at physiologically significant concentrations in serum during an episode of hypoglycemia.

 

Drugs detected by this procedure are:

-The first-generation sulfonylureas-acetohexamide, chlorpropamide, tolazamide, and tolbutamide

-The second-generation sulfonylureas--glimepiride, glipizide, and glyburide

-The meglitinide-repaglinide

 

Drugs designed to make tissues more sensitive to insulin that do not induce hypoglycemia, such as pioglitazone, rosiglitazone, and troglitazone (recently withdrawn from the United States market) are not included in this screen test.

 

Drugs that lower blood glucose through mechanisms not related to stimulation of insulin secretion, such as acarbose, metformin, and miglitol are not included in this screen test.

Method Name

Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)

Reporting Name

Hypoglycemic Agent Scrn, S

Specimen Type

Serum Red

Collection Container/Tube: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 3 mL

Specimen Minimum Volume

1.1 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Red Frozen (preferred) 14 days
  Ambient  14 days
  Refrigerated  14 days

Clinical Information

The metabolic and hormonal profiles of insulinoma and sulfonylurea-induced hypoglycemia are identical. Therefore, in the evaluation of the hypoglycemic patient, the possible use of oral hypoglycemic agents as the cause for low blood glucose and elevated plasma insulin must be considered. Absence of hypoglycemic drugs in blood serum during an episode of low blood glucose should be demonstrated before considering pancreatic exploration for suspected insulinoma.

Reference Values

ACETOHEXAMIDE

Negative: <1,000 ng/mL

 

CHLORPROPAMIDE

Negative: <1,000 ng/mL

 

TOLAZAMIDE

Negative: <20 ng/mL

 

TOLBUTAMIDE

Negative: <50 ng/mL

 

GLIMEPIRIDE

Negative: <20 ng/mL

 

GLIPIZIDE

Negative: <3 ng/mL

 

GLYBURIDE

Negative: <3 ng/mL

 

REPAGLINIDE

Negative: <3 ng/mL

Note: The report indicates a specific drug is positive if that drug is detected at a concentration greater than the sensitivity limit. The test sensitivity limit listed for each drug is lower than the concentration that will cause increased insulin and decreased glucose.

Cautions

Proper interpretation requires that the blood specimen be drawn during or close to the time of a hypoglycemic episode. Drugs will not be detected (and are not likely to be present) if blood is drawn when blood glucose is normal in nondiabetic patients.

 

All drugs that stimulate insulin secretion undergo extensive metabolism before excretion. The parent drug is therefore not present in urine. Blood serum is the specimen of choice for detecting use of the hypoglycemic drugs: urine or plasma is not an acceptable specimen.

 

This test is not intended for therapeutic drug monitoring.

Day(s) Performed

Monday, Wednesday, Friday (9 a.m. cutoff)

Report Available

2 days

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

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

80304

G0479 (if appropriate)

NY State Approved

Yes