Find Locations
For hours, walk-ins and appointments.Unable to load global navigation.
Test Includes
LA-sensitive activated partial thromboplastin time (PTT-LA); dilute Russell viper venom time (dRVVT); dilute prothrombin time (dPT); dPT confirm ratio; thrombin time. If PTT-LA, dRVVT or thrombin time are extended, reflex testing is performed and additional charges/CPT code(s) will apply.
Expected Turnaround Time
2 - 3 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Related Information
Related Documents
For more information, please view the literature below.
Procedures for Hemostasis and Thrombosis: A Clinical Test Compendium
Specimen Requirements
Specimen
Plasma, frozen
Volume
3 mL
Minimum Volume
2 mL (Note: This volume does not allow for repeat testing.)
Container
Blue-top (sodium citrate) tube
Collection
Citrated plasma samples should be collected by double centrifugation. Blood should be collected in a blue-top tube containing 3.2% buffered sodium citrate.1 Evacuated collection tubes must be filled to completion to ensure a proper blood to anticoagulant ratio.2,3 The sample should be mixed immediately by gentle inversion at least six times to ensure adequate mixing of the anticoagulant with the blood. A discard tube is not required prior to collection of coagulation samples.4,5 When noncitrate tubes are collected for other tests, collect sterile and nonadditive (red-top) tubes prior to citrate (blue-top) tubes. Any tube containing an alternate anticoagulant should be collected after the blue-top tube. Gel-barrier tubes and serum tubes with clot initiators should also be collected after the citrate tubes. Centrifuge for 10 minutes and carefully remove 2/3 of the plasma using a plastic transfer pipette, being careful not to disturb the cells. Deliver to a plastic transport tube, cap, and recentrifuge for 10 minutes. Use a second plastic pipette to remove the plasma, staying clear of the platelets at the bottom of the tube. Transfer the plasma into a Labcorp PP transpak frozen purple tube with screw cap (Labcorp No. 49482). Freeze immediately and maintain frozen until tested.
Please print and use the Volume Guide for Coagulation Testing to ensure proper draw volume.
Storage Instructions
Freeze.
Patient Preparation
Ideally, the patient should not be on anticoagulant therapy. Avoid warfarin (Coumadin®) therapy for two weeks prior to the test and heparin, direct Xa, and thrombin inhibitor therapies for about three days prior to testing.
Causes for Rejection
Severe hemolysis; improper labeling; clotted specimen; specimen diluted with IV fluids; samples thawed in transit; improper sample type; sample out of stability
Test Details
Use
Qualitative detection of lupus anticoagulants in plasma6
Methodology
Clot-based clotting time assays
Additional Information
Lupus anticoagulants are antibodies that inhibit one or more of the in vitro phospholipid-dependent tests of coagulation.6-10 Recently, the SCC Subcommittee for the Standardization of Lupus Anticoagulants provided guidelines for the laboratory diagnosis of LA.6 No single screening test can detect all LA-positive patients. The ISTH recommends that any sample suspected of having LA be tested using two or more LA screening tests.6,7 The screening tests commonly used to detect LA assess inhibitors of the intrinsic pathway (aPTT) and the common pathways (dRVVT). The dPT assay screens for phospholipid-dependent inhibitors of a different part of the coagulation cascade, the extrinsic pathway.11 The thrombin time is included to rule out heparin and other thrombin inhibitors.
Footnotes
1. Adcock DM, Kressin DC, Marlar RA. Effect of 3.2% vs 3.8% sodium citrate concentration on routine coagulation testing. Am J Clin Pathol. 1997 Jan; 107(1):105-110. 8980376
2. Reneke J, Etzell J, Leslie S, Ng VL, Gottfried EL. Prolonged prothrombin time and activated partial thromboplastin time due to underfilled specimen tubes with 109 mmol/L (3.2%) citrate anticoagulant. Am J Clin Pathol. 1998 Jun; 109(6):754-757. 9620035
3. National Committee for Clinical Laboratory Standardization. Collection, Transport, and Processing of Blood Specimens for Coagulation Testing and General Performance of Coagulation Assays; Approved Guideline. 5th ed. Villanova, Pa; 2008. NCCLS Document H21-A5:28(5).
4. Gottfried EL, Adachi MM. Prothrombin time and activated partial thromboplastin time can be performed on the first tube. Am J Clin Pathol. 1997 Jun; 107(6):681-683. 9169665
5. McGlasson DL, More L, Best HA, Norris WL, Doe RH, Ray H. Drawing specimens for coagulation testing: Is a second tube necessary? Clin Lab Sci. 1999 May-Jun; 12(3):137-139. 10539100
6. Brandt JT, Triplett DA, Alving B, et al. Criteria for the diagnosis of lupus anticoagulants: An update. On behalf of the Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibody of the Scientific and Standardization Committee of the ISTH. Thromb Haemost. 1995 Dec; 74(4):1185-1190. 8560433
7. Brandt JT, Barna LK, Triplett DA. Laboratory identification of lupus anticoagulants: Results of the Second International Workshop for Identification of Lupus Anticoagulants. On behalf of the Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies of the ISTH. Thromb Haemost. 1995 Dec; 74(6):1597-1603. 8772243
8. Alving BM. The antiphospholipid syndrome: Clinical presentation, diagnosis, and patient management. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. Philadelphia, Pa: WB Saunders Co; 2002:181-196.
9. Levine JS, Branch DW, Rauch J. The aAntiphospholipid syndrome. N Engl J Med. 2002 Mar 7; 346(10):752-763. 11882732
10. Greaves M, Cohen H, MacHin SJ, Mackie I. Guidelines on the investigation and management of the antiphospholipid syndrome. Br J Haematol. 2000 Jun; 109(4):704-715. 10929019
11. Arnout J, Vanrusselt M, Huybrechts E, Vermylen J. Optimization of the dilute prothrombin time for the detection of the lupus anticoagulant by use of a recombinant tissue thromboplastin. Br J Haematol. 1994 May; 87(1):94-99. 7947261
LOINC® Map
| Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
|---|---|---|---|---|---|---|
| 117054 | Lupus Anticoagulant Comp | 103620-1 | 005201 | Dilute Prothrombin Time(dPT) | sec | 75508-2 |
| 117054 | Lupus Anticoagulant Comp | 103620-1 | 005203 | dPT Confirm Ratio | Ratio | 75884-7 |
| 117054 | Lupus Anticoagulant Comp | 103620-1 | 109009 | Thrombin Time | sec | 3243-3 |
| 117054 | Lupus Anticoagulant Comp | 103620-1 | 117003 | PTT-LA | sec | 34571-0 |
| 117054 | Lupus Anticoagulant Comp | 103620-1 | 117891 | dRVVT | sec | 6303-2 |
| 117054 | Lupus Anticoagulant Comp | 103620-1 | 117893 | Lupus Reflex Interpretation | 75514-0 |
| Reflex Table for Thrombin Time | ||||||
|---|---|---|---|---|---|---|
| Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
| Reflex 1 | 117110 | TT Mix+TTN | 117171 | Thrombin Time Mix | sec | 33525-7 |
| Reflex Table for Thrombin Time | ||||||
|---|---|---|---|---|---|---|
| Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
| Reflex 1 | 117110 | TT Mix+TTN | 117203 | Thrombin Neutralization | sec | 46224-2 |
| Reflex Table for PTT-LA | ||||||
|---|---|---|---|---|---|---|
| Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
| Reflex 1 | 117040 | PTT-LA Mix | 117005 | PTT-LA Mix | sec | 75510-8 |
| Reflex 2 | 117020 | Hexagonal Phase Phospholipid | 117842 | Hexagonal Phase Phospholipid | sec | 3282-1 |
| Reflex Table for PTT-LA | ||||||
|---|---|---|---|---|---|---|
| Order Code | Order Name | Result Code | Result Name | UofM | Result LOINC | |
| Reflex 1 | 117040 | PTT-LA Mix | 117005 | PTT-LA Mix | sec | 75510-8 |
| Reflex 2 | 117035 | PTT-LA Incub Mix | 117036 | PTT-LA Incub Mix | sec | 50760-8 |
| Reflex 3 | 117020 | Hexagonal Phase Phospholipid | 117842 | Hexagonal Phase Phospholipid | sec | 3282-1 |
© 2021 Laboratory Corporation of America® Holdings and Lexi-Comp Inc. All Rights Reserved.
CPT Statement/Profile Statement
The LOINC® codes are copyright © 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Permission is granted in perpetuity, without payment of license fees or royalties, to use, copy, or distribute the LOINC® codes for any commercial or non-commercial purpose, subject to the terms under the license agreement found at https://loinc.org/license/. Additional information regarding LOINC® codes can be found at LOINC.org, including the LOINC Manual, which can be downloaded at LOINC.org/downloads/files/LOINCManual.pdf