Test ID CH8BP Chromogenic Factor VIII Inhibitor Bethesda Profile, Plasma
Advisory Information
This test is for detection of presence of specific inhibitors against factor VIII (FVIII). If the presence or type of inhibitor is unknown, APROL / Prolonged Clot Time Profile, Plasma or ALUPP / Lupus Anticoagulant Profile, Plasma should be ordered first.
This test is indicated for testing for FVIII inhibitors in patients being treated with the specific antibody emicizumab (Hemlibra).
Multiple coagulation profile tests are available. See Coagulation Profile Comparison in Special Instructions for testing that is performed with each profile.
Shipping Instructions
Send all vials in the same shipping container.
Specimen Required
See Coagulation Guidelines for Specimen Handling and Processing in Special Instructions.
Patient Preparation: If drawing sample through a port/line, be sure to waste the appropriate amount prior to collection
Specimen Type: Platelet-poor plasma
Collection Container/Tube: Light-blue top (citrate)
Submission Container/Tube: Plastic vials
Specimen Volume: 2 mL in 2 plastic vials, each containing 1 mL
Collection Instructions:
1. Specimen must be drawn prior to factor replacement therapy.
2. Centrifuge, transfer all plasma into a plastic vial, and centrifuge plasma again.
3. Aliquot plasma into 2 separate plastic vials (1 mL in each) leaving 0.25 mL in the bottom of centrifuged vial.
4. Freeze plasma immediately (no longer than 4 hours after collection) at -20° C or, ideally, ≤-40° C.
Additional Information:
1. Double-centrifuged specimen is critical for accurate results as platelet contamination may cause spurious results.
2. If a priority specimen, mark request form, give reason, and request a call-back.
3. Each coagulation assay requested should have its own vial.
Forms
1. Coagulation Patient Information (T675) in Special Instructions.
2. If not ordering electronically, complete, print, and send a Coagulation Test Request (T753) with the specimen.
Useful For
Detecting the presence and titer of a specific factor inhibitor directed against coagulation factor VIII for patients on emicizumab (Hemlibra). This assay is also useful in patients not on emicizumab (Hemlibra)
This test is not useful for detecting the presence of inhibitors directed against other clotting factors and will not detect the presence of lupus anticoagulants.
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
CH8 | Chromogenic FVIII, P | Yes | Yes |
CH8B | Chromogenic FVIII Inhibitor Titer,P | No | Yes |
CH8BI | Chromogenic FVIII Inhibitor Interp | No | Yes |
Special Instructions
Method Name
Chromogenic
Reporting Name
Chromogenic FVIII Inhibitor ProfileSpecimen Type
Plasma Na CitSpecimen Minimum Volume
See Specimen Required
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma Na Cit | Frozen | 14 days |
Reference Values
Chromogenic Factor VIII Activity Assay (CH8)
Adults: 55-200%
Normal, full-term newborn infants or healthy premature infants usually have normal or elevated factor VIII.*
*See Pediatric Hemostasis References section in Coagulation Guidelines for Specimen Handling and Processing in Special Instructions.
BETHESDA TITER (CH8B)
≤0.5 Bethesda Units
Day(s) and Time(s) Performed
Monday through Friday; Varies
Performing Laboratory

Test Classification
See Individual Test IDsCPT Code Information
CH8-85130
CH8B-85335
CH8BI-85390
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CH8BP | Chromogenic FVIII Inhibitor Profile | 95121-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CH8 | Chromogenic FVIII, P | 49865-9 |
CH8B | Chromogenic FVIII Inhibitor Titer,P | 93450-5 |
606844 | Chromogenic FVIII Inhibitor Interp | 95122-8 |
606865 | Reviewed by | 18771-6 |