eMedicine Specialties > Hematology > Coagulation, Hemostasis, and Disorders
Factor II: Treatment & Medication
Updated: Dec 2, 2008
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
Treatment
Medical Care
Treatment of factor II deficiency should be individualized and aimed at restoring circulating factor II to levels sufficient for hemostasis. Levels greater than 30% of normal are usually adequate. Additionally, in patients with acquired factor II deficiency, the underlying cause should be found and treated.
- Infusion of fresh frozen plasma (FFP) is usually sufficient to treat most cases of bleeding. A loading intravenous (IV) dose of 15-20 mL/kg is administered, followed by a maintenance dose of 3-6 mL/kg IV q12-24h.
- Plasma exchange transfusion may be used to increase factor II levels before surgery.
- Prothrombin complex concentrates (PCCs) have also been used to increase factor II levels.35 PCCs contain factors II, VII, IX, and X, along with protein C. PCCs should be used judiciously because of the risk of thromboembolic complications.
- Vitamin K administration may be useful in patients with acquired factor II deficiency.
Consultations
- Hematologists
- Genetic counselors (in patients with congenital factor II deficiency)
Diet
No dietary restrictions are necessary in individuals with factor II deficiency. Patients should be advised to decrease consumption of alcohol to reduce the risk of alcohol-induced liver disease.
Activity
Activity should be regulated based on the severity of the factor II deficiency and the presence or absence of symptoms. Because of the risk of hemorrhage following traumatic injury, activities with high levels of physical contact are not recommended.
Medication
The goals of pharmacotherapy in those with factor II deficiency are to reduce morbidity and to prevent complications.
Blood Products
Blood products are indicated for the correction of abnormal hemostatic parameters.
Fresh frozen plasma
Plasma is the fluid compartment of blood that contains the soluble clotting factors. Indications for using FFP include bleeding in patients with congenital coagulation defects and multiple coagulation factor deficiencies (severe liver disease).
Adult
Loading dose: 15-20 mL/kg IV
Maintenance dose: 3-6 mL/kg IV q12-24h (half-life of factor II is ~3 d)
Pediatric
Administer as in adults.
None reported
Documented hypersensitivity
Pregnancy
A - Fetal risk not revealed in controlled studies in humans
Precautions
Viral contamination and infection are possible, but they are unlikely because of prescreening; may induce an anamnestic response
Prothrombin complex concentrates
Product made from pooled human plasma. Prothrombin complex concentrates contain factors II, VII, IX, X; protein C; and trace amounts of heparin to guard against thrombosis. Currently recommended for patients with coagulation factor inhibitors only.
Adult
Dosages must be clinically determined and are case dependent; the typical dosage is 50-125 U/kg; because of the risk of thrombotic complications, no more than 3 standard doses should be administered in the first 36-48 h
Pediatric
Administer as in adults.
When administered simultaneously with recombinant FVIIa, may lead to thrombotic complications; should not be used in combination with antifibrinolytics, as this combination may increase the risk of thrombosis
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Monitor for thrombotic complications and hypersensitivity reactions; clinical response, PT, and aPTT should be closely monitored throughout the therapy; if there is no clinical response to the therapy with prothrombin complex concentrates, another treatment should be considered.
Vitamins, Fat-Soluble
Fat-soluble vitamins may play essential role in the function of clotting factors.
Phytonadione (AquaMEPHYTON)
Fat-soluble vitamin K absorbed by the gut and stored in the liver. Necessary for the function of clotting factors in the coagulation cascade. Used to replace essential vitamins that are not obtained in sufficient quantities in the diet or to further supplement levels.
Adult
10 mg PO/IV/IM/SC to replete liver stores
Pediatric
1 mg IM as single dose
Antagonizes the effects of warfarin, sodium, and dicumarol
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Ineffective in hereditary hypoprothrombinemia; rapid infusion may result in flushing and a feeling of constriction in the chest; relatively nontoxic, even in massive doses
More on Factor II |
| Overview: Factor II |
| Differential Diagnoses & Workup: Factor II |
Treatment & Medication: Factor II |
| Follow-up: Factor II |
| References |
| Further Reading |
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References
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Further Reading
Related eMedicine Topics
Keywords
factor II, acquired factor II deficiency, inherited factor II deficiency, deficiency of factor II, prothrombin deficiency, hypoprothrombinemia, FII, F II, prothrombin, vitamin K–dependent proenzyme, vitamin K deficiency, prothrombin abnormality, clotting, coagulation, coagulation disorder, blood coagulation cascade, dysprothrombinemia, prothrombin complex concentrates, prothrombin 20210a, thrombophilia
Treatment & Medication: Factor II