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Molecular weight of hydroxyethyl starch: is there an effect on blood coagulation and pharmacokinetics?

Madjdpour, C. ; Dettori, N. ; Frascarolo, P. ; Burki, M. ; Boll, M. ; Fisch, A. ; Bombeli, T. ; Spahn, D. R.

In: British Journal of Anaesthesia, 2005, vol. 94, no. 5, p. 569-576

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    Titre
    • Molecular weight of hydroxyethyl starch: is there an effect on blood coagulation and pharmacokinetics?
    Auteur
    • Madjdpour, C.. Department of Anaesthesiology and
    • Dettori, N.. Department of Anaesthesiology and
    • Frascarolo, P.. Department of Anaesthesiology and
    • Burki, M.. Department of Experimental Surgery, University Hospital Lausanne, Lausanne, Switzerland.
    • Boll, M.. Medical Affairs, B. Braun Melsungen AG, Melsungen, Germany.
    • Fisch, A.. Research Development Liquids, B. Braun Melsungen SA, Crissier, Switzerland
    • Bombeli, T.. Coagulation Laboratory, Division of Haematology, University Hospital of Zürich, Zürich, Switzerland.
    • Spahn, D. R.. Department of Anaesthesiology and
    Type de document
    • Postprint
    Langue
    • Anglais
    Publié dans
    • British Journal of Anaesthesia, 2005, vol. 94, no. 5, p. 569-576. Oxford University Press
    Autre version électronique
    Identifiant OAI-PMH
    • oai:doc.rero.ch:297105
    Summary
    Background. The development of hydroxyethyl starches (HES) with low impact on blood coagulation but higher volume effect compared with the currently used HES solutions is of clinical interest. We hypothesized that high molecular weight, low-substituted HES might possess these properties. Methods. Thirty pigs were infused with three different HES solutions (20 ml kg−1) with the same degree of molar substitution (0.42) but different molecular weights (130, 500 and 900 kDa). Serial blood samples were taken over 24 h and blood coagulation was assessed by Thromboelastograph® analysis and analysis of plasma coagulation. In addition, plasma concentration and in vivo molecular weight were determined and pharmacokinetic data were computed based on a two-compartment model. Results. Thromboelastograph analysis and plasma coagulation tests did not reveal a more pronounced alteration of blood coagulation with HES 500 and HES 900 compared with HES 130. In contrast, HES 500 and HES 900 had a greater area under the plasma concentration-time curve [1542 (142) g min litre−1, P<0.001, 1701 (321) g min litre−1, P<0.001] than HES 130 [1156 (223) g min litre−1] and alpha half life (\batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{t}_{{\alpha}}^{{\frac{1}{2}}}\) \end{document}) was longer for HES 500 [53.8 (8.6) min, P<0.01] and HES 900 [57.1 (12.3) min, P<0.01] than for HES 130 [39.9 (10.7) min]. Beta half life (\batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\mathrm{t}_{{\beta}}^{{\frac{1}{2}}}\) \end{document}), however, was similar for all three types of HES [from 332 (100) to 381 (63) min]. Conclusions. In low-substituted HES, molecular weight is not a key factor in compromising blood coagulation. The longer initial intravascular persistence of high molecular weight low-substituted HES might result in a longer lasting volume effect