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Test ID F9_IS Factor IX Inhibitor Screen, Plasma

Method Name

Only orderable as a reflex. For more information see:

9INHE / Factor IX Inhibitor Evaluation, Plasma

ALUPP / Lupus Anticoagulant Profile, Plasma

ALBLD / Bleeding Diathesis Profile, Limited, Plasma

APROL / Prolonged Clot Time Profile, Plasma

 

Optical Clot-Based

Reporting Name

Factor IX Inhib Scrn

Specimen Type

Plasma Na Cit

Specimen Minimum Volume

2 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Plasma Na Cit Frozen 14 days

Reference Values

Only orderable as a reflex. For more information see:

9INHE / Factor IX Inhibitor Evaluation, Plasma

ALUPP / Lupus Anticoagulant Profile, Plasma

ALBLD / Bleeding Diathesis Profile, Limited, Plasma

APROL / Prolonged Clot Time Profile, Plasma

 

Negative

Day(s) Performed

Monday through Friday

Report Available

1 to 3 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

85335

LOINC Code Information

Test ID Test Order Name Order LOINC Value
F9_IS Factor IX Inhib Scrn 30086-3

 

Result ID Test Result Name Result LOINC Value
7802 Factor IX Inhib Scrn 30086-3

NY State Approved

Yes


Specimen Required


Only orderable as a reflex. For more information see:

9INHE / Factor IX Inhibitor Evaluation, Plasma

ALUPP / Lupus Anticoagulant Profile, Plasma

ALBLD / Bleeding Diathesis Profile, Limited, Plasma

APROL / Prolonged Clot Time Profile, Plasma

 

See Coagulation Guidelines for Specimen Handling and Processing in Special Instructions: Guidelines for Specimen Handling and Processing.


Useful For

Detecting the presence of a specific factor inhibitor directed against coagulation factor IX