Search our extensive Laboratory Test Directory to find test codes, ordering recommendations, specimen stability information, Test Fact Sheets, and more.
Recommendations when to order or not order the test. May include related or preferred tests.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is New York state approved.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
Collect at 60 minutes post-glucose load.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
Gray (sodium fluoride/potassium oxalate).
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Separate plasma from cells within 24 hours. Transport 1 mL plasma. (Min: 0.2 mL)
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Refrigerated.
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
After separation from cells: Ambient: 24 hours; Refrigerated: 1 week; Frozen: 1 year
Methodology
Process(es) used to perform the test.
Quantitative Enzymatic Assay
Performed
Days of the week the test is performed.
Sun-Sat
Reported
Expected turnaround time for a result, beginning when ARUP has received the specimen.
Within 24 hours
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Values > 140 mg/dL constitute a positive screen. Positive screens on pregnant patients should be followed by a diagnostic three-hour oral glucose tolerance test (Glucose Tolerance Test, Pregnancy 0020543).
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Compliance Category
FDA
Note
Additional information related to the test.
Administer 50 g glucola. Do not mix with water unless directions on product label indicate to do so. The patient does not need to be fasting for the screen. During the test period, the patient should remain inactive and receive nothing by mouth (including tobacco); a small sip of water or ice is permissible. Reasons for invalid results include emesis and conditions that delay stomach emptying.
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.