Test Overview
Test Methodology

Chromogenic Substrate Assay

Test Usage

Used to monitor treatment with unfractionated (standard) heparin. Specifically for patients with history of Eliquis (Apixaban) or Xarelto (Rivaroxaban) therapy.

Reference Range *

Due to concurrent or recent therapy with an Anti-Xa inhibitor, the UNFH is measured by an Anti-IIa Assay.
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The therapeutic range for the Adult ACS/AFib and stroke nomograms is 0.2-0.5 IU/mL. The therapeutic range for the Adult DVT/PE nomogram is 0.3-0.7 IU/mL. Patients not being followed with the Adult UMHS nomogram, the therapeutic range for unfractionated heparin is 0.3 to 0.7 IU/mL

* Reference ranges may change over time. Please refer to the original patient report when evaluating results.

Test Details
Days Set Up
Daily, 24 hours
Analytic Time

2 hours

Soft Order Code
UFH2A
MiChart Code
Anti-IIa, Unfractionated Heparin
Laboratory
Hematopathology
Section
Coagulation
STAT Availability

STAT requests for this test will be performed on a STAT basis (supervisory staff approval is not required).

Specimen Requirements
Collection Instructions

Collect specimen in a blue top (citrate 3.2%) tube. Mix by inversion. Specimen should arrive at lab within one hour of collection; transport at room temperature. Alternatively, centrifuge, aliquot plasma into a plastic vial, and freeze the specimen within 1 hour of collection. Transport frozen specimen on dry ice. Collection of the blood through lines that have been previously flushed with heparin should be avoided. If the blood must be drawn through a VAD (vascular access device), the line should be flushed with 5 mL of saline and the first 5 mL of blood or six dead space volumes of the VAD discarded.

Special Handling

Specimen must be received in lab within one hour of collection. Alternatively, aliquot and freeze within 1 hour of collection.

Contraindications
Test is not indicated if the patient is receiving low molecular weight heparin. This test is not indicated for patients on Argatroban or Dabigatran.
Normal Volume
Full 2.7mL tube or 1mL plasma aliquot
Minimum Volume
Full 1.8mL tube or 1mL plasma aliquot
Storage Temperature
Room temperature for whole blood or frozen aliquot of citrated plasma
Rejection Criteria
Specimens will be rejected if not properly filled, clotted, grossly hemolyzed, contaminated with heparin, or received outside acceptable time limits.
Billing
CPT Code
85130
Fee Code
BA017