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Factor II Activity (1:20)

Coagulation

FII activityProthrombin (Factor II) activity

Review status

Currently under review

Pending specialist review and validation.

What it shows

The Factor II 1:20 test measures the functional activity of prothrombin (also called Factor II), a clotting protein produced by your liver with the help of vitamin K. Your plasma is diluted and tested in a clot-based system to see how well Factor II participates in forming a stable clot.

Results are reported as activity in units per milliliter relative to normal plasma. This test is often performed along with screening tests such as PT and aPTT or with other specific factor assays to understand where a clotting problem may be occurring.

Why it matters

Too little Factor II activity can lead to easy bruising, nosebleeds, heavy menstrual bleeding, or bleeding after injuries or procedures. Low activity may be inherited or acquired, such as from vitamin K deficiency, liver disease, certain autoimmune conditions, or medicines that reduce the production or function of clotting proteins.

Your clinician may order this test when screening tests are abnormal, when there is unexplained bleeding, before surgery in someone with bleeding symptoms, or when an inhibitor against Factor II is suspected. It can also help assess the impact of vitamin K antagonist therapy and guide treatment of reversible causes like vitamin K deficiency.

Understanding your results

If your Factor II activity is lower than expected, your clinician will interpret it together with PT, aPTT, mixing studies, and other factor levels to decide whether the cause is a deficiency or an inhibitor. They may review your medicines, check vitamin K status, and evaluate liver function, since these can strongly affect Factor II.

Higher than expected activity is less common and is usually interpreted in the context of your clinical history, medicines, and hormonal status. Follow-up may include repeat confirmation, treatment of reversible causes, or referral to a specialist for further evaluation, including genetic testing if a rare inherited disorder is suspected.

Reference ranges

0.51.5 U/mL
All sexes
0 days – 150 years

Reference intervals vary by laboratory, analyzer, methodology, population, and units. The ranges shown here are for education only. Always interpret your results against the reference interval printed on your own lab report.

Factors that could impact Factor II Activity (1:20)

  • Anticoagulant medicines

    Vitamin K antagonists reduce the liver’s production of Factor II, lowering measured activity. Heparin, direct thrombin inhibitors, and some direct factor Xa inhibitors can interfere with clot-based assays, sometimes causing falsely low activity.

  • Sample collection and handling

    Underfilled citrate tubes, high hematocrit, contamination from heparinized lines, delays to centrifugation or freezing, and improper storage temperature can artifactually change clotting results and lead to inaccurate Factor II activity.

  • Liver and vitamin K status

    Because Factor II is made in the liver using vitamin K, liver disease, malnutrition, malabsorption, prolonged antibiotic use, or cholestasis can lower activity. Correcting vitamin K deficiency may improve results over time.

  • Autoantibodies and inhibitors

    Specific inhibitors to Factor II or antiphospholipid antibodies associated with hypoprothrombinemia can reduce measured activity. Mixing studies and inhibitor screens help distinguish deficiency from an inhibitor effect.

  • Pregnancy and hormones

    Physiologic changes in coagulation during pregnancy and with estrogen-containing therapies can shift clotting factor levels. Your clinician will interpret results in this context and may recommend repeat testing if needed.

  • Recent transfusion or factor products

    Transfusion of plasma or prothrombin complex concentrates can temporarily raise Factor II activity, potentially masking an underlying deficiency. Tell your care team about recent infusions.

2026

References

  1. McGill University Health Centre. (2015, March 01). Factor II 1:20 (Task CD 701455). Laboratory reference ranges.
  2. Clinical and Laboratory Standards Institute. (2008). Collection, transport, and processing of blood specimens for testing plasma-based coagulation assays; approved guideline (5th ed.) (CLSI document H21-A5). Wayne, PA: CLSI.
  3. Kitchen, S., Gray, E., Mackie, I., Baglin, T., & Makris, M. (2014). Measurement of non-coumarin anticoagulants and their effects on tests of haemostasis: Guidance from the British Committee for Standards in Haematology. British Journal of Haematology, 166(6), 830–841.
  4. Peyvandi, F., Menegatti, M., & Palla, R. (2019). Rare bleeding disorders: A practical review. Haemophilia, 25(5), 671–682.