Ordering Recommendation

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Lavender (K2EDTA), pink (K2EDTA), or K3EDTA. Collection tube must be siliconized glass or plastic.

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL plasma to an ARUP standard transport tube and freeze immediately. (Min: 0.5 mL)

Storage/Transport Temperature

CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.

Unacceptable Conditions

Serum, heparinized plasma, tissue, or urine. Grossly hemolyzed specimens.

Remarks
Stability

After separation from cells: Ambient: 3 hours; Refrigerated: 4 hours; Frozen: 10 weeks (No freeze/thaw cycles.)

Methodology

Quantitative Electrochemiluminescent Immunoassay (ECLIA)

Performed

Sun-Sat

Reported

Within 24 hours

Reference Interval

Interpretive Data

This assay measures intact ACTH 1-39; some types of synthetic ACTH and ACTH fragments are not detected by this assay.

Compliance Category

FDA

Note

Hotline History

N/A

CPT Codes

82024

Components

Component Test Code* Component Chart Name LOINC
0070300 Adrenocorticotropic Hormone, LP1 2141-0
* 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.

Aliases

Adrenocorticotropic Hormone, LP1