thromboplastin and Factor-XIII-Deficiency

thromboplastin has been researched along with Factor-XIII-Deficiency* in 5 studies

Reviews

1 review(s) available for thromboplastin and Factor-XIII-Deficiency

ArticleYear
Familial multiple coagulation factor deficiencies. I. Review of the literature: Differentiation of single hereditary disorders associated with multiple factor deficiencies from coincidental concurrence of single factor deficiency states.
    Seminars in thrombosis and hemostasis, 1981,Fall, Volume: 7, Issue:2

    Topics: Blood Coagulation Disorders; Blood Transfusion; Calcium; Factor V Deficiency; Factor VIII; Factor X Deficiency; Factor XI Deficiency; Factor XII Deficiency; Factor XIII Deficiency; Female; Hemophilia A; Hemophilia B; Humans; Hypoprothrombinemias; Male; Pedigree; Thromboplastin

1981

Other Studies

4 other study(ies) available for thromboplastin and Factor-XIII-Deficiency

ArticleYear
In vitro inhibition of factor XIII retards clot formation, reduces clot firmness, and increases fibrinolytic effects in whole blood.
    Anesthesia and analgesia, 2009, Volume: 109, Issue:4

    Thrombelastography has received renewed interest in the perioperative setting. The main determinants of thrombelastographic results are coagulation factor concentrations (various zymogens and fibrinogen) and platelet count; thus, platelet inhibition renders these assays mainly coagulation factor dependent. Assays with and without platelet inhibition are thus increasingly used to trigger and monitor replacement therapy with blood products. In this study, we evaluated the effect of factor XIII inhibition and additional glycoprotein (GP) IIb/IIIa blockade on (platelet-inhibited) whole blood thrombelastography and whether a modified routine assay (using factor XIII antibody) can be used to detect factor XIII deficiency.. Normal whole blood was incubated with increasing amounts of a nonspecific antibody, an anti-GPIIb/IIIa antibody, or a neutralizing anti-factor XIII antibody; samples were analyzed with a tissue factor-activated and platelet-inhibited whole blood thrombelastographic assay. Clotting time, clot formation time, maximum clot firmness, and clot lysis at 60 min were evaluated in triplicate. Also, 25 whole blood routine samples were evaluated for factor XIII deficiency using a new thrombelastographic assay incorporating a factor XIII antibody and using a standard factor XIII assay for comparison.. Although GPIIb/IIIa inhibition did not alter the results of the platelet-inhibited whole blood thrombelastography, factor XIII inhibition significantly reduced maximum clot firmness (P = 0.020) and increased clot formation time (P = 0.025) and clot lysis (P = 0.007), leaving clotting time unchanged; a ceiling effect seemed to be present with increasing antibody concentrations in whole blood (but not plasma). The thrombelastographic assay for factor XIII deficiency (<70% activity) had a 90% sensitivity and negative predictive value (area under receiver operating characteristic curve 0.803, P = 0.0015); for a deficiency <60%, sensitivity and negative predictive value were 100% (area under receiver operating characteristic curve 0.84, P = 0.0037).. Factor XIII has significant impact on platelet-inhibited activated whole blood thrombelastography. This phenomenon should be considered when interpreting thrombelastographic results in the bleeding patient, especially when the results trigger procoagulant therapy. Antibody-mediated factor XIII inhibition can be used to establish thrombelastography-based assays to detect factor XIII deficiency.

    Topics: Abciximab; Antibodies; Antibodies, Monoclonal; Blood Coagulation; Factor XIII; Factor XIII Deficiency; Fibrinolysis; Humans; Immunoglobulin Fab Fragments; Platelet Aggregation Inhibitors; Platelet Glycoprotein GPIIb-IIIa Complex; Predictive Value of Tests; ROC Curve; Sensitivity and Specificity; Thrombelastography; Thromboplastin; Time Factors

2009
Laboratory diagnosis of congenital coagulation defects.
    Clinics in haematology, 1979, Volume: 8, Issue:1

    Topics: Afibrinogenemia; Blood Coagulation Disorders; Blood Coagulation Tests; Factor V Deficiency; Factor VII Deficiency; Factor X Deficiency; Factor XI Deficiency; Factor XII Deficiency; Factor XIII Deficiency; Hemophilia A; Hemophilia B; Humans; Hypoprothrombinemias; Kaolin; Phosphatidylethanolamines; Prekallikrein; Prothrombin Time; Thrombin; Thromboplastin; von Willebrand Diseases

1979
[Studies on congenital factor XIII deficiency and detection of the carrier in his family (author's transl)].
    [Rinsho ketsueki] The Japanese journal of clinical hematology, 1979, Volume: 20, Issue:11

    Topics: Child; Factor XIII Deficiency; Genetic Carrier Screening; Humans; Male; Thromboplastin

1979
Platelet aggregation by Thrombofax.
    Acta Universitatis Carolinae. Medica. Monographia, 1972, Volume: 53

    Topics: Adenosine Diphosphate; Afibrinogenemia; Anti-Inflammatory Agents; Aspirin; Blood Platelets; Citrates; Densitometry; Dose-Response Relationship, Drug; Drug Stability; Drug Storage; Epinephrine; Factor V Deficiency; Factor VII Deficiency; Factor XIII Deficiency; Fatty Acids, Nonesterified; Heparin; Humans; Platelet Adhesiveness; Serum Albumin; Temperature; Thromboplastin; Time Factors

1972