Liver Fibrosis Risk Profile With Hepatic Function Panel, Complete Blood Count (CBC) With Differential, FIB-4, and APRI

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Turnaround Time: Within 1 day
Test Type: 4 mL Serum

Overview:

Use: Screening patients suspected to be at risk for liver fibrosis.

AST to Platelet Ratio Index (APRI) is reported to be a simple, noninvasive, and readily available laboratory test index that can stratify patients with HCV and Non-Alcoholic Fatty Liver Disease (NAFLD) who are at high or low risk for significant fibrosis and cirrhosis with high degree of accurancy.

FIB-4 index is reported to be a simple, accurate, noninvasive, and readily available laboratory test index that can help in evaluation of patients with HCV and Non-Alcoholic Fatty Liver Disease (NAFLD) for the presence of liver fibrosis indication for liver biopsy, and other liver-related complications.

Limitations: Clumping may cause false low platelet count. Platelet satellitism around neutrophils will cause a pseudothrombocytopenia. RBC or WBC fragments including fragmented fragile leukemic cells and neutrophil pseudoplatelets may cause falsely elevated counts.

Methodology: See individual test components.

 

Collection Details:

Collection Instructions:

Specimen: Serum and whole blood

Volume: 4 mL (serum); fill-tube to capacity (whole blood)

Minimum Volume: 2.5 mL (serum) and 0.5 mL (whole blood) (Note: This volume does not allow for repeat testing.)

Container: Gel-barrier tube or red-top tube and lavender-top (EDTA) tube

Collection: Separate serum from cells within 45 minutes of collection; invert EDTA tube immediately 8 to 10 times once tube is filled at the time of collection.

Storage Instructions: Room temperature.

Causes for Rejection: Serum: Gross hemolysis; improper labeling

Whole blood: Hemolysis; clotted specimen; tube not filled with minimum volume; improper labeling; transfer tubes with whole blood; specimen diluted or contaminated with IV fluid; specimen received with plasma removed; specimen collected in any anticoagulant other than EDTA