The Effectiveness of Continuous Infusion of Factor VIII Concentrate in Patients with Hemophilia
Keywords:
Continuous infusion, Factor VIII, Hemophilia, InhibitorAbstract
Abstract : A continuous infusion of factor VII centrate was given to 9 patients with hemophilia A (FVIII C < 1% to 3.5%) who received orthopedic surgery (8 cases) or had serious bleeding in vital organs (1 case). The ages ranged from 6 to 18 years old. The patient showed good response with a high and steady level of F VIII C. The continuous infusion of 0.046 unickg/h raised the F VIII:C by 1 U/dL (1%). Thrombophlebitis was found in 4 cases which was minimized by the addition of heparin into the reconstituted factor concentrate. Inhibitor was found in 3 cases. However, no excessive bleeding was found. This study showed that the continuous infusion of factor VII concentrate was effective in controlling bleeding disorders in hemophiliac patients. It is recommended
for hospitalized patient with serious bleeding or undergoing surgery.
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Mc Milian CW, Webster WP, Roberts HR, Blythe WB. Continuous intravenous infusion of factor VIII in classic hemophilia. Br J Haematol 1970;18:659-67.
Hathaway WE, Christain MJ, Clarke SL, Hasiba U. Comparison of continuous and intermittent factor VIII concentrate therapy in hemophilia A. Am J Hematol 1984;17:85-8.
Martinowitz U, Schulman S, Gitel S, Horozowski H, Heim M, Varon D. Adjusted dose continuous infusion of factor VIII in patients with hemophilia A. Br J Haematol 1992;82:729-34.
Schulman S, Varon D, Keller N, Gitel S, Martinowitz U. Monoclonal puritied F VIII for continuous infusion stability, microbiological safety and clinical experience. Thromb Haemost 1994;72:403-7.
Schulman S, Gitel S, Martinowitz U. Stability of factor VIII concentrates after reconstitution. Am J Hematol 1994;45:217-23.
Hardisty RM, Macpherson JC. A one-stage factor VIII (antihemophilic globulin) assay and its use on venous blood and capillary plasma. Thromb Diath Haemorrh 1962;7:215-8.
Kasper CK, Aledort MI, Counts RB, et al. A more uniform measurement of factor VIll inhibitor. Thromb Diath Haemorrh 1975;34:869-72.
Martinowitz U, Schulman S. Fibrin sealant in surgery of patients with a hemorrhagic diathesis. Thromb Hemost 1995;74:486-92.
Bonna RD, Weinstein A, Weisman SJ, Bartolomeo A, Rickles FR. The use of continuous infusion of factor concentrates in the treatment of hemophilia. Am J Hematol 1989;32:8-13.
Chuansumrit A, Isarangkura P, Hathirat P, et al. Care of Thai hemophilia from 1969-1991. J Med Asso Thailand 1993;76(suppl2):92-102.
Van Leewan EF, Mauser-Bunschoten EP, van Diken PJ, et al. Disappearance of factor VIII:C antibodies in patients with hemophilia upon frequent administration of factor VIII in intermediate or low dose. Br J Haematol 1986;64:291-7.
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