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Thromb Haemost 2014; 112(02): 424-425
DOI: 10.1160/TH13-12-1045
Letters to the Editor
Schattauer GmbH

Pharmacokinetic properties of recombinant FVIIa in inherited FVII deficiency account for a large volume of distribution at steady state and a prolonged pharmacodynamic effect

Massimo Morfini
1   Agency for Hemophilia and Regional Reference Center for Inherited Bleeding Disorders, Azienda Ospedaliariero – Universitaria Careggi, Florence, Italy
,
Angelika Batorova
2   The National Haemophilia Centre, Institute of Haematology and Blood Transfusion LFUK, University Hospital, Bratislava, Slovakia
,
Guglielmo Mariani
3   Department of Life Sciences and Biotechnology, University of Ferrara, Medical School, Ferrara, Italy
,
Günter Auerswald
4   Klinikum Bremen-Mitte, Professor Hess Children’s Hospital, Bremen, Germany
,
Francesco Bernardi
3   Department of Life Sciences and Biotechnology, University of Ferrara, Medical School, Ferrara, Italy
,
Giovanni Di Minno
5   Department of Clinical and Experimental Medicine, Federico II University, Naples, Italy
,
Alberto Dolce
6   National Institute of Statistics, Palermo, Italy
,
Calogero Fede
6   National Institute of Statistics, Palermo, Italy
,
Muriel Giansily-Blaizot
7   Laboratory of Hematology, University Hospital, Montpellier, France
,
Jörgen Ingerslev
8   Centre for Hemophilia and Thrombosis, Aarhus University Hospital, Skejby, Aarhus, Denmark
,
Uri Martinowitz
9   National Hemophilia Center, Chaim Sheba Medical Center, Tel Hashomer, and Sackler School of Medicine, Tel Aviv University, Israel
,
Mariasanta Napolitano
10   University of Palermo, Haematology Unit, Thrombosis and Hemostasis Reference Regional Center, Palermo, Italy
,
Mirko Pinotti
3   Department of Life Sciences and Biotechnology, University of Ferrara, Medical School, Ferrara, Italy
,
Jean-Francois Schved
7   Laboratory of Hematology, University Hospital, Montpellier, France
,
for the International FVII [IF7] and Seven Treatment Evaluation Registry [STER] Study Groups › Institutsangaben