Preferred initial panel for the evaluation of lung inflammation or injury in various types of interstitial lung disease (ILD).
Quantitative Enzyme-Linked Immunosorbent Assay/ Quantitative Immunoturbidimetric
New York DOH Approval Status
Allow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection. Transfer 3 mL serum to ARUP Standard Transport Tube. (Min: 1.5 mL)
Plasma, CSF, or other body fluids. Contaminated, heat-inactivated, hemolyzed, icteric, or severely lipemic specimens.
Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 month
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)
|Component Test Code*||Component Chart Name||LOINC|
|3001867||Krebs von den Lungen-6||93369-7|
|3001970||Human Surfactant Protein D||74541-4|
- Lung Injury Panel