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F8INH<br />

83102<br />

FX13M<br />

57302<br />

FOGT<br />

Clinical References: 1. Nichols WL, Heit JA: Activated protein C resistance and thrombosis. <strong>Mayo</strong><br />

Clin Proc 1996;71:897-898 2. Dahlback B, Carlsson M, Svensson PJ: Familial thrombophilia due to a<br />

previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C:<br />

prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 1993;90:1004-1008 3. Bertina<br />

RM, Koeleman BP, Koster T, et al: Mutation in blood coagulation factor V associated with resistance to<br />

activated protein C. Nature 1994;369:64-67 4. Grody WW, Griffin JH, Taylor AK, et al: American<br />

college of medical genetics consensus statement on factor V Leiden mutation testing. Genet Med<br />

2001;3:139-148 5. Press RD, Bauer KA, Kujovich JL, Heit JA: Clinical utility of factor V Leiden<br />

(R506Q) testing for the diagnosis and management of thromboembolic disorders. Arch Path Lab Med<br />

2002;126:1304-1318<br />

Factor VIII Inhibitor Evaluation<br />

Clinical Information: Factor VIII inhibitors are IgG antibodies directed against coagulation FVIII<br />

that typically result in development of potentially life-threatening hemorrhage. These antibodies may<br />

develop in 1 of 4 different patient populations: -Patients with congenital FVIII deficiency (hemophilia A)<br />

in response to therapeutic infusions of factor VIII concentrate -Elderly nonhemophiliac patients (not<br />

previously factor VIII deficient) -Women in postpartum period -Patients with other autoimmune illnesses<br />

Useful For: Detecting the presence and titer of a specific factor inhibitor directed against coagulation<br />

factor VIII<br />

Interpretation: Normally, there is no inhibitor, (ie, negative result). 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 VIII ACTIVITY ASSAY<br />

Adults: 55-200%<br />

Normal, full-term newborn infants or healthy premature infants usually have normal or elevated factor<br />

VIII.*<br />

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

FACTOR VIII INHIBITOR SCREEN<br />

Negative<br />

BETHESDA TITER<br />

0 Units<br />

Clinical References: 1. Kasper CK: Treatment of factor VIII inhibitors. Prog Hemost Thromb<br />

1989;9:57-86 2. Peerschke EI, Castellone DD, Ledford-Kraemer M, et al: Laboratory assessment of FVIII<br />

inhibitor titer. Am J Clin Pathol 2009;131(4):552-558 3. Pruthi RK, Nichols WL: Autoimmune factor<br />

VIII inhibitors. Curr Opin Hematol 1999;6(5):314-322<br />

Factor XIII, Qualitative, with Reflex to Factor XIII 1:1 Mix<br />

Reference Values:<br />

Factor XIII, Qualitative: No Lysis<br />

Factor XIII, 1:1 Mix: Not Applicable<br />

<strong>Test</strong> Performed by: ARUP <strong>Laboratories</strong><br />

500 Chipeta Way<br />

Salt Lake City, UT 84108<br />

False Oat Grass, IgE<br />

82379<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 708

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