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Test Code THRMB THROMBOTIC RISK PANEL

Important Note

This test may require pre-authorization or have limited coverage.  Please check with your appropriate insurance carrier to determine any specific requirements.

Additional Codes

Software Test Code
Label Text                                  THRMB                                                 
EPIC LAB20139
Label Text  CTHRMB - Chemistry Portion of Panel

Performing Laboratory

NorDx Laboratories

Mayo Laboratories

Useful For

Diagnosing thrombotic disorders

Panel includes:

Antithrombin III Activity

Factor V Leiden Mutation

Fibrinogen

Hematocrit

Homocysteine, Total

Silica Screen

Silica Confirmation

DRVVT Screen

DRVVT Confirmation

Partial Thromboplastin Time (PTT)

Protein C Activity

Protein S Antigen

Prothrombin Gene (G20210A)

INR, plasma

Thrombin Time

CTHRMB labeled specimens:

Beta-2-Glycoprotein, IgG, IgM

Cardiolipin Antibodies, IgA, IgG, IgM

Interpretation

If an abnormal lupus screen is detected the following tests will be performed at an additional cost:

DRVVT Mixing Assay

Silica Mixing Study

PTT using reagent more sensitive to factor deficiencies (Dade Actin FS)

Thrombin Time

If the thrombin time is greater than 30, a Reptilase Time will be performed.

Tests may be ordered individually.

Method Name

Chemiluminescent Microparticle Immunoassay (CMIA)

Clauss Clot-Based Assay

Enzyme Linked Immunosorbent Assay (ELISA)

Impedance

Polymerase Chain Reaction (PCR) with DNA probes

Synthetic Substrate (Chromogenics)

Reference Values

An interpretive report will be issued

Days and Times Test Performed

Monday through Friday

Varies

Report Available

14-21 Days

Specimen Type

Submit all of the following:

~ Plasma

~ Serum

~ Whole Blood

Preferred Container

Lavender Top Tube (EDTA) – Collect 3 tubes 

Light Blue Top Tube (Sodium Citrate) – Collect 3 tubes.  **Citrate tubes must be filled--short draws will be rejected

Serum Separator Tube (SST)- Collect 1 tube

Minimum Volume

Collecting minimum volumes can result in a need for sample recollection, and/or a delay in results. Minimum volumes are subjective and cannot account for all aspects of specimen and testing needs. Refer to the Preferred Volume section for optimal volumes for laboratory specimens.

 

Light Blue Top Tube (Sodium Citrate) – Collect 3 tubes.

Lavender Top Tube (EDTA) – Collect 2 tubes.  Each must have at least 2.0 mL.

Serum Separator Tube (SST)- Collect 1 tube.  Must have at least 4.0 mL.

Specimen Collection and Handling

BLOOD, PLASMA, AND SERUM ARE REQUIRED FOR THIS TEST:

 

BLOOD FOR FACTOR 5 LEIDEN and PROTHROMBIN 20210:

1. Draw blood in a lavender-top (EDTA) tube

2. Send 5.0 mL of EDTA whole blood at ambient temperature.

 

PLASMA FOR HOMOCYSTEINE, TOTAL:

1. Draw blood in a lavender-top (EDTA) tube from a fasting patient.

2. IMMEDIATELY spin down and IMMEDIATELY separate plasma from cells.

3. Send 1.0 mL of plasma refrigerated in a plastic screw-capped vial.

 

BLOOD FOR HEMATOCRIT:

1. Draw blood in a lavender-top (EDTA) tube.

2. Mix specimen well.

3. Send a minimum of 1mL EDTA whole blood refrigerated.

4. This hematocrit is a non-reportable internal test to be run at no charge. This is done to rule out abnormal results from blue-top tubes due to a high hematocrit (55%).

5. If a high hematocrit is detected, the client will be contacted to determine the need for a recollect in properly adjusted blue-top tubes. A coagulation pathologist will assess this need with the client.

 

PLASMA FOR ANTITHROMBIN III, FIBRINOGEN, LUPUS ANTICOAGULANT, PROTEIN C and S, REPTILASE TIME, THROMBIN TIME, INR, and PTT:

Collect specimen(s) as follows:

1. Draw blood in 3 light blue-top (3.2% sodium citrate) tube(s). Tube(s) must be full upon collection.

2. Separate plasma from cells as soon as possible within 4 hours of collection in a centrifuge at 2,500 rpm for 15 minutes or 3,000 rpm for 10 minutes.

3. Using a plastic transfer pipette (do not use a glass pipette) decant the plasma to a screw-capped, plastic (polypropylene) vial. Glass vials will not be accepted.

4. Spin the plasma again at 2,500 rpm for 15 minutes or 3,000 rpm for 10 minutes. Note: Double spinning the specimen ensures platelet poor plasma (<10,000 uL)

5. Divide the plasma into as many 0.5-1.0 mL aliquots as possible and cap the vial(s) tightly.

6. Place tubes upright and flash freeze specimen(s) immediately at ≤ – 20° C or below.

7. Three frozen aliquots should be forwarded to Scarborough Referrals for Protein C activity and Protein S antigen. 

8. Send specimen(s) FROZEN on dry ice.

NOTE: Label all specimens appropriately (serum or plasma).

 

SERUM FOR CARDIOLIPIN ANTIBODIES and BETA-2-GLYCOPROTEIN ANTIBODIES:

1. Draw blood in either a plain, red-top tube or a serum separator tube.

2. Spin down and send 3.0 mL of serum.

TO PROCESS:

1. Label all specimens appropriately (serum or plasma).
Thrombotic Risk Panel Test Components

Thrombotic Risk Panel Processing Checklist

Thrombotic Risk Panel Specimen Overview

Coagulation Double Spin Process

Click here to view the Procedure for Collecting a Specimen from an A-line

Specimen Stability Information

Specimen Type: Plasma

Must be spun/separated within: 4 Hours

Note: Whole blood that remains capped and unspun is stable for up to 4 hours when stored at room temperature (18 – 24°C). Frozen plasma is stable 2 weeks @ -20°C and 12 months @ -70°C. Blue top tubes for coag assays must not be refrigerated or placed on ice.

Specimen Type: Serum

Refrigerated: 48 Hours

Must be spun/separated within: 2 Hours

Specimen Type: Whole Blood

Refrigerated: 24 Hours

Add On Capable

Not Permitted

Advance Beneficiary Notice Requirements

This test, when ordered on Medicare patients, is subject to the National Coverage Determination (NCD) policies. Please verify that the diagnosis code (ICD code) you have chosen demonstrates medical necessity for the test as documented in the physician’s patient record. The CMS web site is available to assist you with this verification. A properly executed Advance Beneficiary Notice (ABN) must be submitted with the specimen if medical necessity is not demonstrated by the ICD code chosen.

CPT Code Information

CPT Code

CPT Description

CPT Disclaimer

81240 F2 (Prothrombin, Coagulation Factor Il) Gene Analysis, 20210G>A Variant  
81241 F5 (Coagulation Factor V) Gene Analysis, Leiden Variant  
83090 Homocysteine, Quantitative  
84285 Assay of Silica, Quantitative if Indicated
85300 Clotting Inhibitors or Anticoagulants, Antithrombin III, Activity  
85303 Clotting Inhibitors or Anticoagulants, Protein C, Activity  
85306 Clotting Inhibitors or Anticoagulants, Protein S, Free  
85384 Fibrinogen, Activity  
85610 Prothrombin Time  
85613 Russell Viper Venom Time (Includes Venom); Diluted if Indicated
85670 Thrombin Time, Plasma  
85730 Thromboplastin Time, Partial (PTT), Plasma or Whole Blood  
85732 Thromboplastin Time, Partial (PTT), Plasma Fractions, Each  
86146 x2 Beta-2-glycoprotein antibody, each  
86147 x3 Cardiolipin (Phospholipid) Antibody, Each Ig Class  

Performing Laboratory Location

NorDx Laboratories

Acceptable Alternative Container(s)

Red Top Tube (for SST only)

Rejection Information

Underfilled Citrate tubes (<90%), clotted, or grossly hemolyzed samples.

Clinical Significance

This test is will include a pathologist interpretation. The physician professional component will be billed separately by the consulting physician.