Successful treatment of patients with von Willebrand disease using a high-purity double-virus inactivated factor VIII/von Willebrand factor concentrate (Immunate®)

被引:19
作者
Auerswald, G
Eberspächer, B
Engl, W
Güthner, C
Koksch, M
Kreuz, W
Nimtz, A
Pindur, G
Scheel, H
Schreiber, JD
Siekmann, J
Turecek, PL
Wolf, HH
机构
[1] Baxter Deutschland GmbH, Heidelberg, Germany
[2] Prof Hess Kinderklin, Bremen, Germany
[3] Univ Leipzig, Innere Med Klin, Leipzig, Germany
[4] Univ Frankfurt, Zentrum Kinderheilkunde, D-6000 Frankfurt, Germany
[5] Kinderklin Klinkum Frankfurt, Frankfurt, Germany
[6] Univ Klin Saarlandes, Homburg, Germany
[7] Univ Halle Wittenberg, Klin Innere Med 4, Halle An Der Saale, Germany
[8] Univ Ulm, Klin & Poliklin, Abt Innere Med 3, Ulm, Germany
[9] Baxter AG, Vienna, Austria
关键词
von Willebrand disease; surgery; acute bleeds; Immunate; clinical efficacy;
D O I
10.1055/s-2002-27822
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fourteen patients with different types of von Willebrand disease (vWD) having acute bleeds or elective surgery were treated with Immunate(R), a double-virus inactivated factor VIII/von Willebrand factor (FVIII/vWF) concentrate. The concentrate was applied as a bolus or via continuous infusion. FVIII activity (FVIIIc), vWF antigen (vWF:Ag), ristocetin cofactor activity (vWF:RCo), collagen binding activity (vWF:CB), activated partial thromboplastin time (aPTT), and von Willebrand multimers (vW-multimers) were monitored for 48 hours. Pharmacokinetic analyses were performed. The clinical efficacy was rated excellent or good. Bleeding complications occurred in 3 patients due to an additional FXIII deficiency in one patient, to a surgically induced bleed in another patient, and a rather short substitution period in the third patient. There were no serious adverse experiences. One patient showed a phlebitic reaction at the site of venous access after more than 100 hours of continuous infusion, requiring a change to application via bolus.
引用
收藏
页码:203 / 213
页数:11
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