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antithrombin III |
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antithrombin /an·ti·throm·bin/ (-throm´bin) any naturally occurring or therapeutically administered substance that neutralizes the action of thrombin and thus limits or restricts blood coagulation.
antithrombin I fibrin, referring to its capacity to adsorb thrombin and thus neutralize it. antithrombin III a plasma α of the serpin family that inactivates thrombin and also inhibits certain coagulation factors and kallikrein. Inherited deficiency is associated with recurrent deep vein thrombosis and pulmonary emboli; the complications are prevented and treated with a preparation of antithrombin III from pooled human plasma. antithrombin [an″te-throm´bin] any naturally occurring or therapeutically administered substance that neutralizes the action of thrombin and thus limits or restricts blood coagulation. antithrombin I fibrin, referring to the capacity of fibrin to adsorb thrombin and thus neutralize it. antithrombin III a naturally occurring inhibitor of blood coagulation; it is an α2-globulin member of the serpin group, synthesized in the liver and found in the plasma and various extravascular sites. It inactivates thrombin as well as certain coagulation factors and kallikrein. Inherited deficiency of the protein, an autosomal dominant disorder, is associated with recurrent deep vein thrombosis and pulmonary emboli. Complications from the disorder are prevented and, in conjunction with heparin, treated with a preparation of antithrombin III from pooled human plasma, administered intravenously.
antithrombin III, human (AT-III, heparin cofactor 1) Thrombate III Pharmacologic class: Blood derivative, coagulation inhibitor Therapeutic class: Antithrombin Pregnancy risk category B ActionInactivates thrombin and activated forms of factors IXa, Xa, XIa, and XIIa, thereby inhibiting coagulation and thromboembolism formation AvailabilityInjection: 500 international units, 1,000 international units ⊘Indications and dosages ➣ Thromboembolism related to AT-III deficiency Adults: Initial dosage is individualized to amount required to increase AT-III activity to 120% of normal (determined 20 minutes after administration). Usual infusion rate is 50 to a maximum of 100 international units/minute I.V. Dosage calculation is based on anticipated 1.4% increase in plasma AT-III activity produced by 1 international unit/kg of body weight. Use this formula to calculate dosage: Required dosage (international units) equals desired activity (%) minus baseline AT-III activity (%) multiplied by weight (kg) divided by 1.4 (international units/kg). Maintenance dosage is individualized to amount required to maintain AT-III activity at 80% of normal. ContraindicationsNone PrecautionsUse cautiously in: Administration• Reconstitute drug concentrate with 10 ml of sterile water, normal saline solution, or dextrose 5% in water.
Adverse reactionsCNS: dizziness, light-headedness, headache CV: vasodilation, reduced blood pressure, chest pain EENT: perception of "film" over eyes GI: nausea, sensation of intestinal fullness GU: diuresis Musculoskeletal: muscle cramps Respiratory: dyspnea, shortness of breath Skin: urticaria, oozing lesions, hives, hematoma Other: foul taste, chills, fever InteractionsDrug-drug. Heparin: increased anticoagulant effect Patient monitoring• Monitor AT-III activity levels regularly. Patient teaching☞ Instruct patient to immediately report chest tightness, dizziness, and fever. antithrombin III Hematology A 58 kD α2-glycoprotein with a single polypeptide chain that inactivates serine proteases–thrombin and other coagulation proteins including factor Xa, IXa, kallikrein and others by an
irreversible heparin-dependent reaction Function AT III dissolves blood clots that normally form within the circulation; heparin's anticoagulant activity hinges on activation of AT-III; AT-III-deficient individuals do not benefit from heparin
therapy; ↓ AT-III may be a congenital AD condition, or acquired, occurring in DIC–due to 'consumption' or in liver disease–due to ↓ AT-III production, resulting in an ↑ risk of coagulation; AT III is ↓ in
congenital deficiency, liver transplant, DIC, nephrotic syndrome, cirrhosis, chonic liver disease, carcinoma, mid-menstrual cycle; AT III is defective in 0.14% to 0.5% of the general population. See Hereditary thrombophilia, Recombinant human
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