Liver Fibrosis, Chronic Viral Hepatitis (Echosens FibroMeter)

2005661
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Enhanced Report
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Supplemental Resources
Ordering Recommendation

Noninvasive, serum surrogate marker test for assessment of liver fibrosis in patients with chronic viral hepatitis.

Mnemonic
FIBRO V
Methodology

Quantitative Nephelometry/Quantitative Enzymatic/Quantitative Spectrophotometry/Automated Cell Count/ Electromagnetic Mechanical Clot Detection

Performed

Tue, Thu

Reported

1-5 days

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation

Include an automated platelet count. Platelet count should be performed on the EDTA whole blood sample at the client site within 3 days of submission for testing.

Collect

Lavender (EDTA) or Pink (K2EDTA) AND Serum Separator Tube (SST) AND Light Blue (Sodium Citrate)

Specimen Preparation

Separate serum and citrated plasma from cells ASAP or within 2 hours of collection. Do not send the EDTA whole blood to ARUP.
Transfer 3 mL serum to an ARUP Standard Transport Tube. (Min: 1.2 mL)
Transfer 1 mL platelet-poor citrated plasma to an ARUP Standard Transport Tube (Min: 0.5 mL)

Storage/Transport Temperature

Serum: Frozen.
Plasma (Citrated): CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.

Unacceptable Conditions

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

Remarks
Stability

Serum: Ambient: 8 hours; Refrigerated: 1 week; Frozen: 2 weeks
Plasma: Ambient: 24 hours; Refrigerated: Unacceptable; Frozen: 2 weeks

Reference Interval

By report

Interpretive Data

Refer to report.

Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.

Note
Hotline History
N/A
CPT Codes

83883; 84450; 84460; 84520; 82977 (Alt code: 81599)

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Components
Component Test Code* Component Chart Name LOINC
2005664 FibroMeter Platelet Count 26515-7
2005666 Fibrometer Prothrombin Index 6302-4
2005675 FibroMeter Patient Score 77616-1
2005676 Fibrosis Metavir Classification 48794-2
2005677 EER Fibrometer Report 11526-1
2005684 FibroMeter Interpretation 48767-8
2009244 InflaMeter Metavir Classification
2009247 InflaMeter Patient Score
2009248 CirrhoMeter Patient Score
2010928 Aspartate Aminotransferase, FibroMeter 1920-8
2010929 Alanine Aminotransferase, FibroMeter 1742-6
2010930 Gamma Glutamyl Transferase, FibroMeter 2324-2
2010931 Urea Nitrogen, Serum, FibroMeter 3094-0
2010932 Alpha-2-Macroglobulin, FibroMeter 1835-8
* 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
  • FibroSure
Liver Fibrosis, Chronic Viral Hepatitis (Echosens FibroMeter)