Literature DB >> 6440729

Evaluation of the effectiveness of DDAVP in surgery and in bleeding episodes in haemophilia and von Willebrand's disease. A study on 43 patients.

G Mariana, N Ciavarella, M G Mazzucconi, S Antoncecchi, S Solinas, P Ranieri, P Pettini, F Agrestini, F Mandelli.   

Abstract

1-deamino-8-D-arginine-vasopressin (DDAVP), was used in a wide spectrum of clinical situations employing two different dosages (0.3 and 0.4 microgram/kg b.w.) for the management of 43 patients with factor VIII deficiencies--mild and moderate haemophilia A and von Willebrand's disease (vWD). In most instances, the drug was given in association with antifibrinolytics. Twenty-five dental extractions were carried out with two different protocols: one based upon a single infusion and the other based upon three infusions. Bleeding occurred in three patients regardless of the protocol used. The vasopressin analogue promptly stopped bleeding in 12 'spontaneous' open bleeds (haematuria, epistaxis, menometrorrhagia, gum bleeding) and it appears to be also effective in closed bleeds. DDAVP was used to minimize blood loss during surgical interventions and to avoid haemorrhage in the postoperative period. Nine surgical procedures were carried out in six vWD patients and three haemophiliacs. Bleeding occurred late in the postoperative period on one occasion only. No difference was demonstrated between the two doses of the drug either in terms of clinical benefit or rise of factor VIII coagulant activity. The efficacy of DDAVP and the absence of side-effects make this vasopressin analogue worthy of consideration as a reliable alternative to factor VIII concentrates in a wide variety of clinical situations.

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Year:  1984        PMID: 6440729     DOI: 10.1111/j.1365-2257.1984.tb00548.x

Source DB:  PubMed          Journal:  Clin Lab Haematol        ISSN: 0141-9854


  4 in total

Review 1.  The use of desmopressin in acquired haemophilia A: a systematic review.

Authors:  Massimo Franchini; Giuseppe Lippi
Journal:  Blood Transfus       Date:  2011-07-18       Impact factor: 3.443

2.  LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B.

Authors:  Alexandre Kauskot; Sonia Poirault-Chassac; Frédéric Adam; Vincent Muczynski; Gabriel Aymé; Caterina Casari; Jean-Claude Bordet; Christelle Soukaseum; Chantal Rothschild; Valérie Proulle; Audrey Pietrzyk-Nivau; Eliane Berrou; Olivier D Christophe; Jean-Philippe Rosa; Peter J Lenting; Marijke Bryckaert; Cécile V Denis; Dominique Baruch
Journal:  JCI Insight       Date:  2016-10-06

3.  Use of desmopressin in the treatment of hemophilia A: towards a golden jubilee.

Authors:  Pier Mannuccio Mannucci
Journal:  Haematologica       Date:  2018-03       Impact factor: 9.941

4.  Desmopressin in moderate hemophilia A patients: a treatment worth considering.

Authors:  Janneke I Loomans; Marieke J H A Kruip; Manuel Carcao; Shannon Jackson; Alice S van Velzen; Marjolein Peters; Elena Santagostino; Helen Platokouki; Erik Beckers; Jan Voorberg; Johanna G van der Bom; Karin Fijnvandraat
Journal:  Haematologica       Date:  2018-01-05       Impact factor: 9.941

  4 in total

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