Literature DB >> 23937614

Desmopressin (DDAVP) in the management of patients with congenital bleeding disorders.

C Leissinger1, M Carcao, J C Gill, J Journeycake, T Singleton, L Valentino.   

Abstract

Bleeding disorders, including haemophilia, von Willebrand disease, and platelet function abnormalities pose a substantial, ongoing management challenge. Patients with these disorders not only require treatment during bleeding events but also need effective management strategies to prepare for events ranging from minor dental procedures to major surgery and childbirth. Moreover, women with bleeding disorders often require ongoing treatment to prevent menorrhagia during childbearing years. Desmopressin (DDAVP), a synthetic derivative of the antidiuretic hormone l-arginine vasopressin, has become a well-established tool for the management of patients with bleeding disorders in a variety of clinical settings. However, despite the widespread use of DDAVP, the available clinical evidence on its efficacy and safety in these settings is limited, and there has not been a recent comprehensive review of its role in the clinical management of patients with bleeding disorders. As such, this article provides a review of the mechanism of action and pharmacokinetic properties of DDAVP, followed by a concise summary of the available evidence for its use in the treatment and prevention of bleeding.
© 2013 John Wiley & Sons Ltd.

Entities:  

Keywords:  DDAVP; desmopressin; haemophilia A; von Willebrand disease

Mesh:

Substances:

Year:  2013        PMID: 23937614     DOI: 10.1111/hae.12254

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  9 in total

1.  Differences in bleeding phenotype and provider interventions in postmenarchal adolescents when compared to adult women with bleeding disorders and heavy menstrual bleeding.

Authors:  L V Srivaths; Q C Zhang; V R Byams; J E Dietrich; A H James; P A Kouides; R Kulkarni
Journal:  Haemophilia       Date:  2017-09-05       Impact factor: 4.287

2.  New therapies for von Willebrand disease.

Authors:  Pier Mannuccio Mannucci
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

3.  The European guideline on management of major bleeding and coagulopathy following trauma: fifth edition.

Authors:  Donat R Spahn; Bertil Bouillon; Vladimir Cerny; Jacques Duranteau; Daniela Filipescu; Beverley J Hunt; Radko Komadina; Marc Maegele; Giuseppe Nardi; Louis Riddez; Charles-Marc Samama; Jean-Louis Vincent; Rolf Rossaint
Journal:  Crit Care       Date:  2019-03-27       Impact factor: 9.097

Review 4.  New developments in von Willebrand disease.

Authors:  Helen Fogarty; Dearbhla Doherty; James S O'Donnell
Journal:  Br J Haematol       Date:  2020-05-12       Impact factor: 6.998

5.  New therapies for von Willebrand disease.

Authors:  Pier Mannuccio Mannucci
Journal:  Blood Adv       Date:  2019-11-12

Review 6.  Obstacles to Early Diagnosis and Treatment of Inherited von Willebrand Disease: Current Perspectives.

Authors:  Giancarlo Castaman; Silvia Linari
Journal:  J Blood Med       Date:  2021-03-22

7.  [The role of the anesthesiologist in the care of the pregnant woman with Von Willebrand Disease].

Authors:  Hanane Baouahi; Yassine Zerqouni; Mouhcine Doumiri; Nezha Oudghiri; Anas Tazi Saoud
Journal:  Pan Afr Med J       Date:  2015-12-04

8.  Expert consensus on the diagnosis and treatment of thrombocytopenia in adult critical care patients in China.

Authors:  Jing-Chun Song; Shu-Yuan Liu; Feng Zhu; Ai-Qing Wen; Lin-Hao Ma; Wei-Qin Li; Jun Wu
Journal:  Mil Med Res       Date:  2020-04-03

9.  Clinical Efficacy and Safety of Fanhdi®, a Plasma-Derived VWF/Factor VIII Concentrate, in von Willebrand Disease in Spain: A Retrospective Study.

Authors:  Víctor Jiménez-Yuste; María Teresa Alvarez-Román; Ángeles Palomo Bravo; Bernardo J Galmes; Maria Del Mar Nieto Hernández; Olga Benítez Hidalgo; Cristina Marzo Alonso; Noelia Florencia Pérez González; Julia Coll; Ramiro Núñez; Marina Carrasco; Faustino García Candel; Jose Ramon Gonzalez-Porras; Carmen Hernández García; Maria José Varó Castro; Roser Mir
Journal:  Clin Appl Thromb Hemost       Date:  2022 Jan-Dec       Impact factor: 2.389

  9 in total

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