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Factor XI

Coagulation

Coagulation factor XI activityFactor 11FXIPlasma thromboplastin antecedentPTA

Review status

Currently under review

Pending specialist review and validation.

What it shows

The Factor XI test measures the activity of factor XI, a clotting protein made in your liver that helps your blood form stable clots. It is part of the intrinsic pathway of coagulation and works together with several other proteins to stop bleeding after injury or surgery.

Your sample is usually a blood draw collected in a citrate tube and analyzed in a coagulation laboratory. Some labs measure activity, some measure the amount of the protein, and sometimes both are done to help find the cause of a bleeding tendency.

Why it matters

Low factor XI activity can be inherited or acquired and may increase the chance of bleeding, especially with dental work, surgery, or injuries involving tissues that easily bleed. The degree of bleeding does not always match the level, so your personal history and planned procedures matter when decisions are made.

Clinicians order this test when the activated partial thromboplastin time is prolonged, when there is a family history of factor XI deficiency, before procedures in people with possible bleeding disorders, or to investigate unexplained bruising or bleeding. Changes can also be seen with liver disease or conditions that consume clotting factors.

Occasionally, higher levels are seen with inflammation or other physiologic states. Your care team interprets the result in context with other clotting tests, your medications, and your clinical situation.

Understanding your results

Your factor XI result is interpreted alongside your bleeding history, physical exam, and other lab tests such as the activated partial thromboplastin time and levels of other clotting factors. If the activity is lower than expected, your clinician may repeat the test, check the amount of the protein, or perform specialized studies to look for an inhibitor or an acquired cause.

If you have a deficiency, planning for dental work, childbirth, or surgery may involve a hematology team to reduce bleeding risk. Treatment plans are individualized and may include preventive measures or factor replacement products when appropriate. If a result is unexpectedly high or low, a repeat sample and review of medicines that affect clotting are common next steps.

Do not start or stop any medication on your own. Share all prescription drugs, over‑the‑counter products, and supplements with your care team so they can interpret the test accurately and advise you on safe follow‑up.

Reference ranges

0.41.5 U/mL
All sexes
0 days – 1 month
0.71.4 unit/mL
All sexes
0 days – 150 years
0.71.4 U/mL
All sexes
0 days – 150 years
0.51.5 U/mL
All sexes
1 month – 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 XI

  • Specimen collection quality

    Underfilled or clotted citrate tubes, delayed processing, or improper storage can distort factor XI measurements. A clean venipuncture and timely delivery to the lab help ensure reliable results.

  • Anticoagulant medications

    Heparin, direct oral anticoagulants, and other blood thinners can affect clotting assays or their interpretation. Always tell your clinician and the lab about any anticoagulants you take.

  • Liver health

    Because factor XI is made in the liver, conditions such as hepatitis, cirrhosis, or acute liver injury can lower levels. Your provider may check liver tests if results are unexpected.

  • Inflammation and acute illness

    Acute infections, inflammation, or stress can transiently change clotting factor levels. If you were ill at the time of testing, your clinician may recommend repeating the test when recovered.

  • Inherited deficiency

    Some people inherit lower factor XI activity and may have variable bleeding, especially after procedures. Family history and, in some cases, genetic testing can help clarify the cause.

  • Other clotting factor abnormalities

    Deficiencies in multiple factors, vitamin K issues, or the presence of inhibitors can influence results and symptoms. Your team may order a panel of tests to see the full picture.

2026

References

  1. McGill University Health Centre. (2016, March 17). Factor XI (Task CD 18461590). Laboratory reference ranges.
  2. World Federation of Hemophilia. (2012). Factor XI deficiency. Treatment of Hemophilia monograph.
  3. Seligsohn, U. (2014). Factor XI deficiency. In M. P. Adam et al. (Eds.), GeneReviews. University of Washington, Seattle.