Recommendations when to order or not order the test. May include related or preferred tests.
May be used as an adjunct to IGF-1 in diagnosis of growth disorders.
Unique test identifier.
Process(es) used to perform the test.
Quantitative Enzyme-Linked Immunosorbent Assay
Days of the week the test is performed.
Expected turnaround time for a result, beginning when ARUP has received the specimen.
New York DOH Approval Status
Indicates test has been approved by the New York State Department of Health.
This test is New York DOH approved.
Plain Red or Serum Separator Tube (SST).
Allow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube (Min: 0.2 mL). Freeze Immediately.
CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Moderately or grossly hemolyzed or severely lipemic specimens
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Prepubertal (0-11 years old)
Postpubertal (12 years and older)
Background information for test. May include disease information, patient result explanation, recommendations, details of testing, associated diseases, explanation of possible patient results.
Refer to report.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
Additional information related to the test.
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.