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0098275
Substance P, EIA
SUB P
Ordering Recommendation
New York DOH Approval Status
This test is not New York state approved. There are no New York state-approved laboratories available. Submit a Non-Permitted Laboratory Request Form (NPL) to the NYDOH prior to collection of specimen. If NPL is approved by NYDOH, and sample is received at ARUP, testing will be performed.
Specimen Required
Patient Preparation
Collect
Serum separator tube (SST).
Specimen Preparation
Separate serum from cells ASAP or within 2 hours of collection. Transfer 5 mL serum to ARUP standard transport tube and freeze immediately. (Min: 1 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.
Storage/Transport Temperature
CRITICAL FROZEN.
Unacceptable Conditions
Remarks
Stability
Ambient: Unacceptable; Refrigerated: Unacceptable; Frozen: 1 month
Methodology
Quantitative Enzyme Immunoassay (EIA)
Performed
Varies
Reported
6-13 days
Reference Interval
By report
Interpretive Data
Compliance Category
Performed by non-ARUP Laboratory
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
83520
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0098275 | Substance P, EIA | 2971-0 |
* 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
Substance P, EIA
BioAgilytix Diagnostics
