Sign in →

Test Code LAB3784 Direct Oral Anticoagulant (DOAC) Screen

Clinical System Name

Direct Oral Anticoagulant (DOAC) Screen

Description

The Direct Oral Anticoagulants (DOAC) screen is intended to rapidly identify patients who may be taking direct oral anticoagulants. This information may be useful in making decisions about performing surgery or treating with fibrinolytic agents. Direct Xa Inhibitor Screen will detect direct Xa inhibitors, while the thrombin time will detect direct thrombin inhibitors (DTI).

This screen does not indicate amount of specific DOAC present.

Panel Includes (3 separately reported results):

  • Direct Xa Inhibitor Screen (units/mL)
  • Thrombin Time (TT) (seconds)
  • Anticoagulant Screen Interpretation

 

Direct Xa Inhibitor Screen
(Anti-Xa units/mL)
Thrombin Time
(TT sec)
Anticoagulant Screen Interpretation Notes
≥0.10 >25 Heparin presence likely; cannot rule out presence of direct oral anticoagulant. Recommend specimen re-draw and repeat testing.  
<0.10 >25 Direct Thrombin inhibitor (DTI) (e.g. dabigatran) likely present. Order specific drug level if indicated  
<0.10 ≤25 No detectable factor Xa inhibitor or direct thrombin inhibitor present  
0.10 - 0.30 ≤25 Low level factor Xa inhibitor likely present (e.g apixaban, rivaroxaban, edoxaban, enoxaparin, and/or fondaparinux). Order specific drug level if indicated.  Direct Xa inhibitor screen and direct Xa drug level may not be valid after administration of andexanet alfa.
>0.30 ≤25 Factor Xa inhibitor likely present (e.g. apixaban, rivaroxaban, edoxaban, enoxaparin, and/or fondaparinux). Order specific drug level if indicated.  Direct Xa inhibitor screen and direct Xa drug level may not be valid after administration of andexanet alfa.

A significantly elevated Direct Xa result may indicate presence of direct Xa inhibitor (apixaban, rivaroxaban, edoxaban, enoxaparin, and/or fondaparinux), heparin or abnormal fibrin. Order specific drug level if indicated. Presence of direct Xa inhibitor or heparin is excluded with a direct Xa inhibitor level of <0.1 units/mL.
 
A significantly elevated Thrombin Time (TT) result may indicate presence of direct thrombin inhibitor (Dabigatran, bivalirudin, and/or argatroban), heparin or abnormal fibrin. Order specific drug level if indicated. Presence of direct thrombin inhibitor or heparin unlikely with a normal TT.

Sample Requirements

Specimen: Whole Blood

Container(s): Lt Blue/Citrate

Required Vol: (1) 1.8 mL or (1) 2.7 mL

Minimum Vol: N

 

Note:  This is enough for a PT, PTT, TT, and Fibrinogen to be run on the same sample.

 

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.

Processing Instructions

Deliver whole blood to Coag bench. Coag Technologist will process.

 

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

Spin: Y

Aliquot: Y

Storage location: Core 14 Freezer ( -70 C).

 

Specimen should be centrifuged within one hour of collection. Transfer upper 3/4 layer of plasma to plastic tube affixed with large Epic aliquot label. Do not pool. Assay immediately.

Stability

Specimen Type Temperature Time
Citrated platelet-poor plasma Room temp ≤4 h
  Refrigerated N
  Frozen   -20 C or -70 C ≤3 m

 

Performing Laboratory

Seattle Children's Laboratory    

 

Department

Department:  Coagulation

Phone Number: 206 987-2617 (Client Services)

 

 

Synonyms

LAB3784

DOAC

DOAC Screen

Direct Xa Inhibitor Screen

Anti-Xa Inhibitor Screen

EPIC Order Code 1230121854

Availability

STAT Performed TAT
Y

Daily

1 h

 

Methodology

Method: Chromogenic Substrate by STA-R MAX

Analytical Volume: 1 mL plasma

This is enough for a PT, PTT, DOAC Screen, and Fibrinogen on the same sample.

 

Limitations: This assay requires antithrombin III (ATIII) in patient's plasma. Low level of ATIII may underestimate the heparin level.

Results affected by moderate lipemia, moderate hemolysis, and moderate icterus.

High hematocrit greater than or equal to 56% requires a citrate adjusted tube.

CPT Codes

85520

85670

Therapeutic Range

N/A

Order specific drug level if indicated. 

DOAC activity is reported in Anti-Xa IU/mL (Anti-Xa International Units/mL).

Critical Value

N/A

Critical or elevated results do not necessarily correlate with anticoagulant concentration. Order specific drug level if indicated.

Related Tests