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Mayo Test Catalog, (Sorted By Test Name) - Mayo Medical ...

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F_9<br />

9065<br />

FACTV<br />

9054<br />

disorders, certain antibiotic therapies, some malignancies, and old age. Inhibitors of factor VIII coagulant<br />

activity are the most commonly occurring of the specific factor inhibitors.<br />

Useful For: Detection and quantitation of inhibitor to factor II<br />

Interpretation: Normally, there is no inhibitor, ie, negative. If the screening assays indicate the<br />

presence of an inhibitor, it will be quantitated and reported in Bethesda (or equivalent) units.<br />

Reference Values:<br />

FACTOR II ACTIVITY ASSAY<br />

Adults: 75-145%<br />

Normal, full-term newborn infants or healthy premature infants may have decreased levels (> or<br />

=25%) which may remain below adult levels for > or =180 days postnatal.*<br />

*See Pediatric Hemostasis References in Coagulation Studies in Special Instructions.<br />

FACTOR II INHIBITOR SCREEN<br />

Negative<br />

Clinical References: 1. Feinstein DI: Acquired inhibitors of blood coagulation. In Hematology:<br />

Basic Principles and Practice. Edited by R Hoffman, EJ Benz Jr, SJ Shattil, et al. New York,<br />

Livingstone Press, 1991, pp 1380-1394 2. Kasper CK: Treatment of factor VIII inhibitors. Prog Hemost<br />

Thromb 1989;9:57-86<br />

Coagulation Factor IX Activity Assay, Plasma<br />

Clinical Information: Factor IX is a vitamin K-dependent serine protease synthesized in the liver<br />

and participates in the intrinsic coagulation pathway. Its biological half-life is 18 to 24 hours.<br />

Congenital deficiency inherited as an X-linked recessive bleeding disorder (hemophilia B). Severe<br />

deficiency ( or =180 days postnatal.*<br />

*See Pediatric Hemostasis References in Coagulation Studies in Special Instructions.<br />

Clinical References: 1. Barrowcliffe TW, Raut S, Sands D, Hubbard AR: Coagulation and<br />

chromogenic assays of factor VIII activity: general aspects, standardization, and recommendations.<br />

Semin Thromb Hemost 2002 Jun;28(3):247-256 2. Franchini M, Lippi G, Favaloro EJ: Acquired<br />

inhibitors of coagulation factors: part II. Semin Thromb Hemost 2012 Jul;38(5):447-453 3. Carcao MD:<br />

The diagnosis and management of congenital hemophilia. Semin Thromb Hemost 2012<br />

Oct;38(7):727-734<br />

Coagulation Factor V Activity Assay, Plasma<br />

Clinical Information: Factor V is a vitamin K-independent protein synthesized in the liver and in<br />

other tissues (endothelium, megakaryocytes/platelets). In its thrombin-activated form (factor Va), it<br />

serves as an essential cofactor in the prothrombinase enzyme complex which converts prothrombin to<br />

thrombin (the prothrombinase complex consists of the enzyme, activated factor X, factor Va cofactor, a<br />

phospholipid surface, and calcium). Deficiency of factor V may cause prolonged prothrombin time and<br />

Current as of January 3, 2013 2:22 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong>Laboratories.com Page 489

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