A monoclonally-purified factor VIII (FVIII) concentrate, containing little von Willebrand factor (vWF), was infused to 11 patients with severe von Willebrand disease and unmeasurable levels of plasma vWF. In comparison with the historical data obtained infusing hemophiliacs in the same conditions, monoclonally-purified FVIII had a significantly shorter half-life and faster clearance from plasma but similar in vivo recovery and volume of distribution. Two additional patients with severe von Willebrand disease were also infused with recombinant FVIII totally devoid of vWF. Half-life was very short and in vivo recovery low, with a larger volume of distribution than for monoclonally-purified FVIII. We conclude that in patients with severe von Willebrand disease the small amounts of vWF contained in the monoclonally-purified FVIII concentrate are not sufficient to stabilize infused FVIII, nor to support the normal circulation of endogenous FVIII that these patients produce at a normal rate.

PHARMACOKINETICS OF MONOCLONALLY-PURIFIED AND RECOMBINANT F VIII IN PATIENTS WITH SEVERE VON WILLWBRAND DISEASE / Morfini, M; Mannucci, Pm; Tenconi, Pm; Longo, G; Mazzucconi, Maria Gabriella; Rodeghiero, F; Ciavarella, N; DE ROSA, V; Arter, A.. - In: THROMBOSIS AND HAEMOSTASIS. - ISSN 0340-6245. - 70:(1993), pp. 270-272.

PHARMACOKINETICS OF MONOCLONALLY-PURIFIED AND RECOMBINANT F VIII IN PATIENTS WITH SEVERE VON WILLWBRAND DISEASE

MAZZUCCONI, Maria Gabriella;
1993

Abstract

A monoclonally-purified factor VIII (FVIII) concentrate, containing little von Willebrand factor (vWF), was infused to 11 patients with severe von Willebrand disease and unmeasurable levels of plasma vWF. In comparison with the historical data obtained infusing hemophiliacs in the same conditions, monoclonally-purified FVIII had a significantly shorter half-life and faster clearance from plasma but similar in vivo recovery and volume of distribution. Two additional patients with severe von Willebrand disease were also infused with recombinant FVIII totally devoid of vWF. Half-life was very short and in vivo recovery low, with a larger volume of distribution than for monoclonally-purified FVIII. We conclude that in patients with severe von Willebrand disease the small amounts of vWF contained in the monoclonally-purified FVIII concentrate are not sufficient to stabilize infused FVIII, nor to support the normal circulation of endogenous FVIII that these patients produce at a normal rate.
1993
01 Pubblicazione su rivista::01a Articolo in rivista
PHARMACOKINETICS OF MONOCLONALLY-PURIFIED AND RECOMBINANT F VIII IN PATIENTS WITH SEVERE VON WILLWBRAND DISEASE / Morfini, M; Mannucci, Pm; Tenconi, Pm; Longo, G; Mazzucconi, Maria Gabriella; Rodeghiero, F; Ciavarella, N; DE ROSA, V; Arter, A.. - In: THROMBOSIS AND HAEMOSTASIS. - ISSN 0340-6245. - 70:(1993), pp. 270-272.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/89110
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