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Coagulation Factor assays
Short Description : Coagulation Factor
Also known as : [Coagulation assays],[Factor 10 (Coagulation factor assay)],[Factor 11(Coagulation factor assay)],[Factor 12(Coagulation factor assay)],[Factor 13(Coagulation factor assay)],[Factor 7 (Coagulation factor assay)],[Factor assays],[Factor II assay],[Factor V Assay],[Factor VII Assay (Coagulation factor assay)],[Factor X Assay],[Factor XI Assay],[Factor XII Assay],[Factor XIII Assay],[FII],[FV],[FVII (Coagulation factor assay )],[FVIII (Coagulation factor assay )],[FX],[FXI],[FXII],[FXIII]


Blood
Test performed by: LabPLUS Haematology


Specimen Collection

Assays are available for all coagulation factors. Please discuss with Technical Specialist of the haemostasis laboratory, Haematology Registrar, or Haematologist.

For Factor VIII and Factor iX assays, please refer to:

Factor VIII/Factor IX


Citrate

2.7 mL Adult Citrate Blood

or


2xCitrate

1.8 mL 2xCitrate Blood

  • If the specimen is collected from outside Auckland Hospital: send 2x 1.5 ml plasma aliquot, frozen.

  • Reference Intervals

    Normal Reference Intervals:

    Factors VIII and IX 55 - 150%
    All others 50 - 200%

    Factors Uncertainty of measurement
    VIII , IX, XI , XII 18%
    II , V , VII , x , XIII 12%

    • Paediatric reference intervals are age stratified and given on the result report



    Turnaround Time: Within 2 weeks

    Unless URGENT


    Diagnostic Use and Interpretation

    Factor assays are generally used to identify the cause of bleeding disorders. However, factors II, VII and VIII are included in the investigation of thrombosis.

    The Chromogenic FVIII is used in suspected mild haemophilia A and not usually required for management. Requests for Chromogenic FVIII must be referred through a Haematologist or Haemophilia Centre.

    See Bleeding History

    Limitations of procedure:

    Factor assays may be affected by sample activation or the presence of inhibitors.

    Interpretation:

    Coagulation factors may be reduced due to defective production (congenital or acquired defects), consumption (DIC), dilution (massive transfusion), destruction (specific inhibitors), and in the case of factors II, VII, IX, or X, vitamin K deficiency/warfarin ingestion.


    Contact Information

    For further information contact the Haematology laboratory (Ext 22067) or:

    Dr Nicola Eaddy Ext 22005
    Dr Peter Bradbeer Ext 22062
    Dr Anna Ruskova Ext 22137
    Dr Nikhil Rabade Ext 22071



    Last updated at 13:09:28 11/09/2024