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In-vitro-Untersuchungen zur Sicherheit und Stabilität von Faktor-Konzentraten während kontinuierlicher Infusion

  • Conference paper
27. Hämophilie-Symposion Hamburg 1996

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Zusammenfassung

Die Substitutionstherapie für Patienten mit Hämophilie A oder B bzw. schwerem v.-Willebrand-Syndrom erfolgt üblicherweise durch intravenöse Applikation von Bolusinjektionen und ergibt typischerweise starke Schwankungen der minimalen und maximalen Plasmalevel des verabreichten Faktorkonzentrates im Laufe eines Behandlungstages und in Abhängigkeit von der Halbwertszeit des jeweiligen Konzentrats [1].

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Literatur

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Authors
  1. M. von Depka Prondzinski
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  2. J. Edel
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  3. M. Barthels
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  4. I. Scharrer
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  5. A. Ganser
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Editor information

Editors and Affiliations

  1. Zentr. d. Inn. Med., Med. Klinik I, Universitätsklinikum, Theodor-Stern-Kai 7, D-60590, Frankfurt am Main, Deutschland

    Inge Scharrer

  2. Hämostaseologische Abteilung, Med. Univ.-Klinik Innenstadt, Ziemssenstraße 1a, D-80336, München, Deutschland

    Wolfgang Schramm

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© 1998 Springer-Verlag Berlin Heidelberg

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von Depka Prondzinski, M., Edel, J., Barthels, M., Scharrer, I., Ganser, A. (1998). In-vitro-Untersuchungen zur Sicherheit und Stabilität von Faktor-Konzentraten während kontinuierlicher Infusion. In: Scharrer, I., Schramm, W. (eds) 27. Hämophilie-Symposion Hamburg 1996. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-80403-8_32

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  • DOI: https://doi.org/10.1007/978-3-642-80403-8_32

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-62915-3

  • Online ISBN: 978-3-642-80403-8

  • eBook Packages: Springer Book Archive

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