By Inge Scharrer, Wolfgang Schramm, G. Auerswald, A. Kurth, J. Oldenburg, W. Schramm, B. Zieger
This publication comprises the contribution to the thirty sixth Hemophilia Symposium, Hamburg 2005. the most issues are epidemiolgy, hemophilia treatment, orthopedic therapy in hemophiliacs, hemostaseologic analysis and pediatric hemostaseology. the amount is rounded off through various loose papers and posters on hemophilia, inhibitors in hemophilia and diagnostics.
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Extra resources for 36th Hemophilia Symposium Hamburg 2005: Epidemiology; Hemophilia Therapy - Management of Bleedings and Inhibitors; Orthopedic Treatment in Hemophiliacs; ... Pediatric Hemostaseology; Free Lectures
Van DK, van der Bom JG, Lenting PJ, de Groot PG, Mauser-Bunschoten EP, Roosendaal G, Grobbee DE, van den Berg HM. Factor VIII half-life and clinical phenotype of severe hemophilia A. Haematologica 2005; 90: 494–8. 29. Vlot AJ, Mauser-Bunschoten EP, Zarkova AG, Haan E, Kruitwagen CL, Sixma JJ, van den Berg HM. The half-life of infused factor VIII is shorter in hemophilic patients with blood group O than in those with blood group A. Thromb Haemost 2000; 83: 65–9. 30. Bjorkman S, Berntorp E. Pharmacokinetics of coagulation factors: clinical relevance for patients with haemophilia.
Prof. Landesklinikum St. Pölten, A-St. Pölten I. Epidemiology Chairmen: L. Gürtler (Greifswald) W. Schramm (Munich) HIV Infection and Causes of Death in Patients with Hemophilia in Germany (Year 2004/2005 Survey) H. Krebs, and W. Schramm on Behalf of the Participating German Hemophilia centers Introduction The annually survey »HIV Infection and Causes of Death in Patients with Hemophilia in Germany« already goes along with a fine tradition. Already in the late 1970s Professor Landbeck began to survey annually hemophiliacs in West Germany for causes of death and the prevalence of diseases.
Regarding data back to 1999 the inhibitor prevalence observed in our cohort is slightly declining as depicted in Figure 3. Combining these data with further data of other authors and surveys presented at the Hamburg Hemophilia-Symposium since 1978 (see Fig. 5 % successful immune tole- H. Krebs, W. Schramm % F:VIII inhibitors 6 Fig. 3. Prevalence of patients with hemophilia A and inhibitors since 1999 rance therapies per year there is also no indication of an increasing prevalence of inhibitors in patients with hemophilia A.