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Test Code HEXLA Hexagonal Lupus Anticoagulant, Plasma


Specimen Required


Only orderable as part of a reflex. For more information see:

ALUPP / Lupus Anticoagulant Profile, Plasma

ACBL / Bleeding Diathesis Profile, Comprehensive, Plasma

ALBLD / Bleeding Diathesis Profile, Limited, Plasma

AATHR / Thrombophilia Profile, Plasma and Whole Blood

APROL / Prolonged Clot Time Profile, Plasma

ADIC / Disseminated Intravascular Coagulation/Intravascular Coagulation and Fibrinolysis (DIC/ICF) Profile, Plasma


Useful For

Confirming or excluding the presence of a lupus anticoagulant (LA), in conjunction with other appropriate coagulation tests

 

Differentiating between deficiencies or inhibitors of specific coagulation factors and LA inhibitors

 

Evaluating a prolonged activated partial thromboplastin time resulting from inhibition

Method Name

Only orderable as part of a reflex. For more information see:

ALUPP / Lupus Anticoagulant Profile, Plasma

ACBL / Bleeding Diathesis Profile, Comprehensive, Plasma

ALBLD / Bleeding Diathesis Profile, Limited, Plasma

AATHR / Thrombophilia Profile, Plasma and Whole Blood

APROL / Prolonged Clot Time Profile, Plasma

ADIC / Disseminated Intravascular Coagulation/Intravascular Coagulation and Fibrinolysis (DIC/ICF) Profile, Plasma

 

Spectrophotometric

Reporting Name

HEX LA, P

Specimen Type

Plasma Na Cit

Specimen Stability Information

Specimen Type Temperature Time Special Container
Plasma Na Cit Frozen 60 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject

Clinical Information

Lupus anticoagulant (LA) is one of several antibodies referred to as antiphospholipid antibodies (APA). Lupus anticoagulants are immunoglobulins (IgG, IgM, IgA, or a combination of these) that interfere with specific coagulation factor-phospholipid interactions, typically causing prolongation of one or more phospholipid-dependent clotting time tests (eg, activated partial thromboplastin time [aPTT]; dilute Russell's viper venom time due to inhibition). The characteristic in vitro inhibition caused by the presence of LA inhibitors can be overcome by additional phospholipid, which can be used to confirm the presence of LA. However, the most common in-vivo clinical manifestations of presence of APA are vascular thrombosis and recurrent miscarriage, among other organ manifestations. The combination of clinical manifestations and persistent presence of APA satisfies the criteria for APA syndrome. The hexagonal LA assay system enhances the sensitivity and specificity of aPTT-based LA detection by employing:

1. A partial thromboplastin that is more responsive to LA than many other reagents.

2. Inverted hexagonal phase phospholipid for neutralization of LA inhibition.

Reference Values

Only orderable as part of a reflex. For more information see:

ALUPP / Lupus Anticoagulant Profile, Plasma

ACBL / Bleeding Diathesis Profile, Comprehensive, Plasma

ALBLD / Bleeding Diathesis Profile, Limited, Plasma

AATHR / Thrombophilia Profile, Plasma and Whole Blood

APROL / Prolonged Clot Time Profile, Plasma

ADIC / Disseminated Intravascular Coagulation/Intravascular Coagulation and Fibrinolysis (DIC/ICF) Profile, Plasma

 

<13 seconds

Day(s) Performed

Monday through Friday

Report Available

2 to 4 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

85598