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, PSpecimen Type
Plasma Na CitSpecimen 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 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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