The natural history of factor VIII:C inhibitors in patients with hemophilia A: a national cooperative study. II. Observations on the initial development of factor VIII:C inhibitors. 1988

C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
University of Connecticut School of Medicine.

During a 4-year multicenter cooperative study of acquired factor VIII inhibitors in persons with hemophilia A, new inhibitors were detected in 31 of 1,306 patients who entered the study without an inhibitor or the history of an inhibitor. The incidence of new inhibitors was eight per 1,000 patient-years of observation. The factor VIII:C level before inhibitor development was less than or equal to 0.03 U/mL in 29 individuals and 0.06 U/mL and 0.07 U/mL in the remaining two. Factor VIII:Ag levels were measured in 27 individuals and were less than 0.03 U/mL in 23 and 0.05 to 0.11 U/mL in the remaining four. Maximum inhibitor levels ranged from 1.0 to 9,044 Bethesda U/mL. In seven patients under the age of 20, relatively weak inhibitors (none higher than 4.3 Bethesda U/mL) were detected on only a single occasion despite continued factor VIII challenge. In the other 24 patients with inhibitors detected on multiple occasions, 50% had appeared by age 20 and 71% by age 30. Seventeen of the 31 inhibitors, including 12 of 15 with maximum values greater than 10 Bethesda U/mL, developed within 75 exposure days to factor VIII.

UI MeSH Term Description Entries
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D005169 Factor VIII Factor VIII of blood coagulation. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin. Coagulation Factor VIII,Factor VIII Clotting Antigen,Factor VIII Coagulant Antigen,Factor VIII Procoagulant Activity,Thromboplastinogen,Blood Coagulation Factor VIII,F VIII-C,Factor 8,Factor 8 C,Factor Eight,Factor VIIIC,Hyate-C,Hyatt-C,F VIII C,Hyate C,HyateC,Hyatt C,HyattC
D006467 Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. Factor VIII Deficiency,Hemophilia,Autosomal Hemophilia A,Classic Hemophilia,Deficiency, Factor VIII,Factor 8 Deficiency, Congenital,Factor VIII Deficiency, Congenital,Haemophilia,Hemophilia A, Congenital,Hemophilia, Classic,As, Autosomal Hemophilia,Autosomal Hemophilia As,Classic Hemophilias,Congenital Hemophilia A,Congenital Hemophilia As,Hemophilia A, Autosomal,Hemophilia As,Hemophilia As, Autosomal,Hemophilia As, Congenital,Hemophilias, Classic
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000367 Age Factors Age as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or the effect of a circumstance. It is used with human or animal concepts but should be differentiated from AGING, a physiological process, and TIME FACTORS which refers only to the passage of time. Age Reporting,Age Factor,Factor, Age,Factors, Age
D000906 Antibodies Immunoglobulin molecules having a specific amino acid sequence by virtue of which they interact only with the ANTIGEN (or a very similar shape) that induced their synthesis in cells of the lymphoid series (especially PLASMA CELLS).
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor

Related Publications

C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
January 1985, Archivos de investigacion medica,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
February 1984, Blood,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
January 1984, Progress in clinical and biological research,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
December 2009, International journal of laboratory hematology,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
June 1987, Archives of internal medicine,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
January 1996, Acta haematologica,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
August 1984, Annals of internal medicine,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
January 1971, Nordisk medicin,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
December 1985, Revue francaise de transfusion et immuno-hematologie,
C W McMillan, and S S Shapiro, and D Whitehurst, and L W Hoyer, and A V Rao, and J Lazerson
March 1996, American journal of hematology,
Copied contents to your clipboard!