Thromb Haemost 1987; 58(03): 896-898
DOI: 10.1055/s-0038-1646011
Original Article
Schattauer GmbH Stuttgart

Concentrated DDAVP: Further Improvement in the Management of Mild Factor VIII Deficiencies

A Ghirardini
The Department of Human Biopathology, Section of Hematology, University of Roma “La Sapienza”, Rome, Italy
,
G Mariani
The Department of Human Biopathology, Section of Hematology, University of Roma “La Sapienza”, Rome, Italy
,
G lacopino
The Department of Human Biopathology, Section of Hematology, University of Roma “La Sapienza”, Rome, Italy
,
M C Tirindelli
The Department of Human Biopathology, Section of Hematology, University of Roma “La Sapienza”, Rome, Italy
,
S Solinas
The Department of Human Biopathology, Section of Hematology, University of Roma “La Sapienza”, Rome, Italy
,
T Moretti
The Department of Human Biopathology, Section of Hematology, University of Roma “La Sapienza”, Rome, Italy
› Author Affiliations
Further Information

Publication History

Received 11 November 1986

Accepted after revision 09 June 1987

Publication Date:
28 June 2018 (online)

Summary

This study was carried out to evaluate the pharmacological efficacy of a new concentrated 1 Deamino - (8-D-arginine) - vasopressin (DDAVP) preparation. Concentrated DDAVP (C- DDAVP), (40 μg/mL) was given subcutaneously (s.c.) in hemophilia and von Willebrand Disease (vWD), and the response was evaluated in terms of factor VIII/vWF (VUI/von Willebrand Factor) complex response. This response was also compared to that obtained using the currently available commercial preparation (4 μg/mL) given either s.c. or intravenously (i. v.). The maximal f. VIII response after s.c. C-DDAVP was reached one hour after the injection (x:3.6 times the resting values) with an average decline of 15% at two hours. The response to s.c. C- DDAVP in patients with hemophilia was slightly better than thut obtained with the diluted brand, but the difference did not reach any statistical significance even when the schedules were compared in the same patients. In type I (placed normal subtype) vWD, a higher response in terms of factor VIII :C increase in comparison with hemophiliacs was obtained. Doth Ristocetin cofactor activity (RiCof) and bleeding time responded to this vasopressin analogue, when administered subcutaneously.

 
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