Ordering Recommendations

Only intended for use in patients with non-alcoholic liver disease (NAFLD); results may be inaccurate in patients with other etiologies of liver disease.

Orderable SIM Number(s)

334163

Synonyms

  • Nonalcoholic Fatty Liver Disease
  • Noninvasive Liver Biopsy
  • Fatty Liver Disease
  • Steatohepatitis
  • NAFLD
  • FibroSure
  • LAB123395

ARUP Test Code

2012521

Patient Preparation

Overnight fasting specimen is required.

Collect

Lavender (EDTA) or Pink (K2EDTA) for platelet count AND Serum Separator Tube (SST).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 2 mL serum to an ARUP Standard Transport Tube. (Min: 1.2 mL)

Storage/Transport Temperature

Serum: Frozen. Do not send the EDTA whole blood to ARUP.

*For Clinics:
Please send EDTA sample to ARL refrigerated.


*EDTA sample ONLY needed for platelet count. ARL hematology department will perform testing to obtain count.

Unacceptable Conditions

Hemolyzed specimens. All required specimens not received. No platelet count received. No weight received.

Stability (from collection to initiation)

Serum: Ambient: 24 hours; Refrigerated: 1 week; Frozen: 2 weeks

Special Handling Instructions

 Weight is required and must be entered when test is ordered.

Remarks

This test requires an automated platelet count performed on the EDTA whole blood sample at the client site. Include the platelet count with the patient test submission information. This test requires the patient's weight (in pounds). Include the patient's weight with the sample submission.

Reference Interval

By report

Interpretive Data

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.

Notes

This test requires an automated platelet count performed on the EDTA whole blood sample at the client site. Include the platelet count with the patient test submission information. This test requires the patient's weight (in pounds). Include the patient's weight with the sample submission.

Compare to FibroSure.

CPT Codes

84450; 84460; 82728; 82947 (Alt code: 81599)

Billable SIM Number(s)


3018445003 (CPT 84450)
3018446003 (CPT 84460)
3018272803 (CPT 82728)
3018294702 (CPT 82947)


 

LOINC

  • 26515-7
  • 77616-1
  • 1920-8
  • 1742-6
  • 2276-4
  • 2345-7
  • 29463-7
  • 11526-1
  • 48767-8
  • 48794-2
Overview

Ordering Recommendations

Only intended for use in patients with non-alcoholic liver disease (NAFLD); results may be inaccurate in patients with other etiologies of liver disease.

Orderable SIM Number(s)

334163

Synonyms

  • Nonalcoholic Fatty Liver Disease
  • Noninvasive Liver Biopsy
  • Fatty Liver Disease
  • Steatohepatitis
  • NAFLD
  • FibroSure
  • LAB123395

ARUP Test Code

2012521
Specimen

Patient Preparation

Overnight fasting specimen is required.

Collect

Lavender (EDTA) or Pink (K2EDTA) for platelet count AND Serum Separator Tube (SST).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 2 mL serum to an ARUP Standard Transport Tube. (Min: 1.2 mL)

Storage/Transport Temperature

Serum: Frozen. Do not send the EDTA whole blood to ARUP.

*For Clinics:
Please send EDTA sample to ARL refrigerated.


*EDTA sample ONLY needed for platelet count. ARL hematology department will perform testing to obtain count.

Unacceptable Conditions

Hemolyzed specimens. All required specimens not received. No platelet count received. No weight received.

Stability (from collection to initiation)

Serum: Ambient: 24 hours; Refrigerated: 1 week; Frozen: 2 weeks

Special Handling Instructions

 Weight is required and must be entered when test is ordered.

Remarks

This test requires an automated platelet count performed on the EDTA whole blood sample at the client site. Include the platelet count with the patient test submission information. This test requires the patient's weight (in pounds). Include the patient's weight with the sample submission.
Interpretive

Reference Interval

By report

Interpretive Data

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.

Notes

This test requires an automated platelet count performed on the EDTA whole blood sample at the client site. Include the platelet count with the patient test submission information. This test requires the patient's weight (in pounds). Include the patient's weight with the sample submission.

Compare to FibroSure.
Coding

CPT Codes

84450; 84460; 82728; 82947 (Alt code: 81599)

Billable SIM Number(s)


3018445003 (CPT 84450)
3018446003 (CPT 84460)
3018272803 (CPT 82728)
3018294702 (CPT 82947)


 

LOINC

  • 26515-7
  • 77616-1
  • 1920-8
  • 1742-6
  • 2276-4
  • 2345-7
  • 29463-7
  • 11526-1
  • 48767-8
  • 48794-2