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Introduction ⬇

The prothrombin fragment 1 + 2 (F1 + 2) is the amino terminus fragment liberated from the prothrombin molecule when it is activated by factor Xa to form thrombin. Thrombin may be rapidly inactivated by AT III. Prothrombin F1 + 2, however, has a half-life of about 1.5 hours, making it a useful marker for activated coagulation.

Prothrombin F1 + 2 is used to detect activation of the coagulation system before actual thrombosis occurs. It is used to identify patients with low-grade intravascular coagulation (DIC) and to judge the effectiveness of oral anticoagulant therapy. F1 + 2 levels may assist in the study of the hypercoagulable states and in the assessment of thrombotic risk.

Normal Findings ⬆ ⬇

7.4–102.9 μg/L or 0.2–2.78 nmol/L

Levels rise slightly with age older than 45 years.

Procedure ⬆ ⬇

  1. Draw a 5-mL sample of venous blood into a blue-topped (sodium citrate anticoagulant) Vacutainer tube. Label the specimen with the patient’s name, date and time of collection, and test(s) ordered.

  2. Use the two-tube technique. (Some methods may use lithium heparin.)

Clinical Implications ⬆ ⬇

Increased prothrombin F1 + 2 is found in the following:

  1. DIC (early)

  2. Congenital deficiencies of AT III

  3. Congenital deficiencies of protein S and protein C

  4. Leukemias

  5. Severe liver disease

  6. Post MI

Interventions ⬆ ⬇

Pretest Patient Care

  1. Explain test purpose and procedure.

  2. Avoid prolonged use of tourniquet.

  3. Follow guidelines in Chapter 1 for safe, effective, informed pretest care.

Posttest Patient Care

  1. Review test results; report and record findings. Modify the nursing care plan as needed. Counsel the patient regarding abnormal findings; explain the need for possible follow-up testing and treatment. Monitor for DIC and thrombosis.

  2. Follow guidelines in Chapter 1 for safe, effective, informed posttest care.

  3. Have the patient resume normal activities.

Interfering Factors ⬆

  1. Levels will be high in the immediate postoperative period.

  2. Decreased with oral anticoagulants (warfarin)

  3. Decreased in patients treated with AT III