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Test Code LAB3943 Thromboelastograph, Heparin Neutralized

Important Note

Notify the Laboratory at x7-2727 before collecting or sending this test to ensure timely results.

Clinical System Name

Thromboelastograph, Heparin Neutralized

Synonyms

Thromboelastograph, Heparin reversal

LAB3943

TEG

TEG6s

TEG HR, TEG -HR

TEG HN,  TEG -HN

Description

Please see the TEG Quick Guide for Providers

 

The TEG6s Global Hemostasis cartridge with Heparin Neutralization provides comparative time to clot with and without heparinase to identify heparin effects, evaluates clot strength (fibrinogen and platelet contribution), and measures lysis time. The TEG6s instrument with the Global Hemostasis – HN cartridge assesses blood viscoelastic properties using resonance technology, exposing the blood to a fixed vibration frequency range upon adding calcium and exposure to kaolin, kaolin and heparinase, kaolin with tissue factor and heparinase, kaolin and tissue factor with a platelet inhibitor abciximab and heparinase. In addition to coagulation factor levels, TEG results may be influenced by platelet count, hematocrit, and other hemostatic variables. Accurate results require proper specimen collection; underfilled tubes or improper sample handling may lead to inaccurate results. TEG6s assays are not validated for monitoring therapeutic anticoagulants. For anticoagulation monitoring, drug-specific assays are recommended.

 

Results can be viewed in Epic upon test completion. Anesthesia can view results in real-time by launching TEG Manager (access in Citrix Workspace with your SCH network username and password). For TEG Manager access issues, please submit a ServiceNow ticket. 

Sample Requirements

Specimen: Whole Blood

Acceptable Container(s):  Lt. Blue/Citrate, (1) 1.3 mL or  (1) 1.8 mL or  (1) 2.7 mL.

Required Volume: Tubes must be filled to ensure the blood-to-anticoagulant ratio. Overfilled, underfilled, or clotted tubes are not accepted for this test.

 

Note: Cannot be shared with other coagulation tests.

 

Preferred method of collection is venipuncture with vacuum fill. Test results are affected by incorrect blood volume. Use of a Vascular Access Device for the collection of coag testing is not recommended. Please review the Coagulation Lab Collection Job Aid for detailed instructions.

 

Stability

Specimen Type Temperature Time
Whole blood Room temp ≤ 2 hours
  Refrigerated N
  Frozen N

 

Availability

STAT Performed TAT
Y daily 2 h

 

Processing Instructions

Deliver whole blood to the Coag bench and place in the TEG rack. Coag Technologist will process. Do not centrifuge sample. Testing from the OR must be initiated as soon as possible. Perform testing immediately. 

 

Reject due to: clotted, insufficient quantity (underfill), or improper collection (overfill).

Spin :N

Aliquot :N

Storage location: Core 5 Fridge

 

 

Off-site collection: Cannot be collected outside Children's Main Campus. Do not collect at Seattle Children's Regional Clinic locations.

Performing Laboratory

Seattle Children's Laboratory    

Department

Department:   Coagulation

 

Phone Number: 206 987-2617 (Client Services)

Methodology

Method: TEG6s harmonic resonance elasticity. 

Analytical Volume: 400 µL whole blood

Limitations: Results may be influenced by anticoagulants (e.g. bivalirudin, heparin), hematocrit, and platelet count. Viscoelastic testing (TEG) is not a specific or validated assay for monitoring therapeutic anticoagulation. Drug-specific assays (e.g., bivalirudin level or unfractionated heparin activity) should be used for anticoagulation monitoring, when applicable. Improper specimen collection (e.g., underfilled tubes, hemolysis) may lead to inaccurate results.

 

TEG Manager is an accessory application that provides remote viewing of TEG analyzer test results and administration of all connected analyzers. Anesthesia can launch TEG Manager (access in Citrix Workspace with your SCH network username and password); other teams can view results in Epic upon test completion. 

 

CK: Kaolin is a standardized reagent consisting of dry Kaolin  and 0.85% Saline solution. Kaolin -activated tests methods are used to reduce variability and to reduce the running time of a native whole blood sample. Use of these particles of hydrated aluminum silicate shortens the coagulation time because Kaolin acts as a contact surface activator (intrinsic pathway), which activates Factor XII and platelets and stimulates the reserve clotting ability of a blood sample. Kaolin is combined with CaCl2 to neutralize any sodium citrate in the blood

 

CKH: Heparin is commonly used as an anticoagulant in surgical procedures. Even in very low concentrations of heparin, fractions of IU/mL of blood, can noticeably increase the R time and can even completely anticoagulate the blood, making it difficult if not impossible to monitor developing coagulopathies that are masked by high levels of therapeutic heparin. The addition of heparinase in the assay cartridge neutralizes the effect of heparin in the sample. CaCl2 is included to neutralize any sodium citrate in the blood. 

 

CRTH: RapidTEG maximally accelerates the clotting process by simultaneously activating the intrinsic and extrinsic coagulation pathways using a high concentration of Kaolin and Tissue Factor (TF). This closely reflects the physiological clotting process and yields results significantly faster than the native, Kaolin, and/or TF activated test. The addition of heparinase in the assay cartridge neutralizes the effects of heparin in the sample. CaCl2 is included to neutralize any sodium citrate in the blood. 

 

 CFFH: The Functional Fibrinogen reagent activates the extrinsic pathway using tissue factor and inhibits platelet aggregation using a platelet inhibitor that binds to GPIIb/IIIa receptors. By excluding the platelet aggregation contribution to clot strength (MA), the reagent measures fibrinogen contribution. The addition of heparinase in the assay cartridge neutralizes the effects of heparin in the sample. Functional Fibrinogen is combined with CaCl2 to neutralize any sodium citrate in the blood. 

Reference Range

CK - R 3.7 - 9.3 minutes
CK - MA 49.8 - 71.3 milimeters
CKH - R 3.6 - 9.2 minutes
CKH - LY30 0.0 - 4.7 %
CRTH 50.4 - 71.7 milimeters
CFFH 13.3 - 32.2 milimeters

 

CPT Codes

85390

Critical Values

Not defined for this test.