Accès à distance ? S'identifier sur le proxy UCLouvain
Practical aspects of DDAVP use in patients with von Willebrand Disease undergoing invasive procedures: a European survey.
Primary tabs
Document type | Article de périodique (Journal article) – Article de recherche |
---|---|
Access type | Accès restreint |
Publication date | 2016 |
Language | Anglais |
Journal information | "Haemophilia : the official journal of the World Federation of Hemophilia" - Vol. 22, no.1, p. 110-120 (2016) |
Peer reviewed | yes |
Publisher | Blackwell Science ((United Kingdom) Oxford) |
issn | 1351-8216 |
e-issn | 1365-2516 |
Publication status | Publié |
Affiliations |
UCL
- SSS/IREC/CARD - Pôle de recherche cardiovasculaire UCL - (SLuc) Service d'hématologie |
MESH Subject | Adolescent ; Adult ; Aged ; Child ; Child, Preschool ; Deamino Arginine Vasopressin ; Europe ; Female ; Humans ; Infant ; Male ; Middle Aged ; Practice Guidelines as Topic ; Surveys and Questionnaires ; Young Adult ; von Willebrand Diseases |
Keywords | DDAVP-haemostatic cover ; surgical intervention ; von Willebrand disease |
Links |
- Sadler, Thrombost Haemost, 84, 160 (2000)
- SADLER J. E., BUDDE U., EIKENBOOM J. C. J., FAVALORO E. J., HILL F. G. H., HOLMBERG L., INGERSLEV J., LEE C. A., LILLICRAP D., MANNUCCI P. M., MAZURIER C., MEYER D., NICHOLS W. L., NISHINO M., PEAKE I. R., RODEGHIERO F., SCHNEPPENHEIM R., RUGGERI Z. M., SRIVASTAVA A., MONTGOMERY R. R., FEDERICI A. B., , Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor, 10.1111/j.1538-7836.2006.02146.x
- Mannucci P. M., Åberg M., Nilsson I. M., Robertson B., Mechanism of Plasminogen Activator and Factor VIII Increase after Vasoactive Drugs, 10.1111/j.1365-2141.1975.tb00521.x
- MARIANA G., CIAVARELLA N., MAZZUCCONI M. G., ANTONCECCHI S., SOLINAS S., RANIERI P., PETTINI P., AGRESTINI F., MANDELLI F., Evaluation of the effectiveness of DDAVP in surgery and in bleeding episodes in haemophilia and von Willebrand's disease. A study on 43 patients, 10.1111/j.1365-2257.1984.tb00548.x
- Mannucci, Prog Hemost Thromb, 8, 19 (1986)
- Kaufmann, Blood, 106, 107 (2000)
- MANNING M, STOEV S, CHINI B, DURROUX T, MOUILLAC B, GUILLON G, Peptide and non-peptide agonists and antagonists for the vasopressin and oxytocin V1a, V1b, V2 and OT receptors: research tools and potential therapeutic agents☆, Advances in Vasopressin and Oxytocin — From Genes to Behaviour to Disease (2008) ISBN:9780444532015 p.473-512, 10.1016/s0079-6123(08)00437-8
- Franchini Massimo, The use of desmopressin as a hemostatic agent: A concise review, 10.1002/ajh.20940
- Evidence levels and grades of evidence grade http://www.bcshguidelines.com/BCSH_PROCESS/EVIDENCE_LEVELS_AND_GRADES_OF_RECOMMENDATION/43_GRADE.html
- García-Matte Raimundo, María Constanza Beltrán M., Ximena Fonseca A., Pamela Zúñiga C., Management of children with inherited mild bleeding disorders undergoing adenotonsillar procedures, 10.1016/j.ijporl.2011.11.024
- SANTORO C., HSU F., DIMICHELE D. M., Haemostasis prophylaxis using single dose desmopressin acetate and extended use epsilon aminocaproic acid for adenotonsillectomy in patients with type 1 von Willebrand disease : DDAVP AND EACA FOR ADENOTONSILLECTOMY IN TYPE 1 VWD PATIENTS, 10.1111/j.1365-2516.2011.02619.x
- Tosetto Alberto, Federici Augusto, Rodeghiero Francesco, Castaman Giancarlo, Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearance, 10.1160/th10-11-0697
- Bornert Fabien, Clauss François, Gros Catherine-Isabelle, Faradji Albert, Schmittbuhl Matthieu, Manière Marie-Cécile, Feki Ahmed, Hemostatic Management in Pediatric Patients With Type I von Willebrand Disease Undergoing Oral Surgery: Case Report and Literature Review, 10.1016/j.joms.2011.03.073
- Witmer Char M., Elden Lisa, Butler Regina B., Manno Catherine S., Raffini Leslie J., Incidence of Bleeding Complications in Pediatric Patients with Type 1 von Willebrand Disease Undergoing Adenotonsillar Procedures, 10.1016/j.jpeds.2009.01.051
- Meschengieser Susana, Woods Adriana, Chuit Roberto, Turdó Karina, Blanco Alicia, Lazzari María, Sánchez-Luceros Analía, Biological and clinical response to desmopressin (DDAVP) in a retrospective cohort study of children with low von Willebrand factor levels and bleeding history, 10.1160/th10-04-0220
- Jiménez-Yuste Victor, Prim María P., De Diego Juan I., Villar Ana, Quintana Manuel, Rabanal Iñaki, Sastre Noelia, Hernández-Navarro Fernando, Otolaryngologic Surgery in Children With von Willebrand Disease, 10.1001/archotol.128.12.1365
- Leissinger C., Becton D., Cornell C., Cox Gill J., High-dose DDAVP intranasal spray (StimateR) for the prevention and treatment of bleeding in patients with mild haemophilia A, mild or moderate type 1 von Willebrand disease and symptomatic carriers of haemophilia A, 10.1046/j.1365-2516.2001.00500.x
- Mannucci Pier Mannuccio, Treatment of von Willebrand's Disease, 10.1056/nejmra040403
- Rodeghiero F., Castaman G., Tosetto A., How I treat von Willebrand disease, 10.1182/blood-2009-01-153296
- Michiels Jan Jacques, van Vliet Huub H. D. M., Berneman Zwi, Gadisseur Alain, van der Planken Marc, Schroyens Wilfried, van der Velden Ann, Budde Ulrich, Intravenous DDAVP and Factor VIII-von Willebrand Factor Concentrate for the Treatment and Prophylaxis of Bleedings in Patients With von Willebrand Disease Type 1, 2 and 3, 10.1177/1076029606296399
- Klaassen Robert J, Halton Jacqueline M, The diagnosis and treatment of von Willebrand disease in children, 10.1093/pch/7.4.245
- Yawn, Am Fam Physician, 80, 1261 (2009)
- NICHOLS W. L., HULTIN M. B., JAMES A. H., MANCO-JOHNSON M. J., MONTGOMERY R. R., ORTEL T. L., RICK M. E., SADLER J. E., WEINSTEIN M., YAWN B. P., von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA), 10.1111/j.1365-2516.2007.01643.x
- Batlle, Haematologica, 97, 2 (2012)
- Pasi K. J., Collins P. W., Keeling D. M., Brown S. A., Cumming A. M., Dolan G. C., Hay C. R. M., Hill F. G. H., Laffan M., Peake I. R., Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization, 10.1111/j.1365-2516.2004.00886.x
- Guidelines of the Nordic Hemophilia Council Nordic guidelines for diagnosis and management of von Willebrand disease
- Mannucci, Blood Transfus, 7, 117 (2009)
- Laffan Mike A., Lester Will, O'Donnell James S., Will Andrew, Tait Robert Campbell, Goodeve Anne, Millar Carolyn M., Keeling David M., The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology, 10.1111/bjh.13064
- Goodeve Anne C., The genetic basis of von Willebrand disease, 10.1016/j.blre.2010.03.003
- Castaman G., Lethagen S., Federici A. B., Tosetto A., Goodeve A., Budde U., Batlle J., Meyer D., Mazurier C., Fressinaud E., Goudemand J., Eikenboom J., Schneppenheim R., Ingerslev J., Vorlova Z., Habart D., Holmberg L., Pasi J., Hill F., Peake I., Rodeghiero F., Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD, 10.1182/blood-2007-08-109231
- Casonato, Thromb Haemost, 81, 224 (1999)
- Mikhail, Expert Rev Hamatol, 1-15 (2014)
- Castaman G., Goodeve A., Eikenboom J., , Principles of care for the diagnosis and treatment of von Willebrand disease, 10.3324/haematol.2012.077263
- Mannucci, Thrombost Haemost, 86, 149 (2001)
- Leissinger C., Carcao M., Gill J. C., Journeycake J., Singleton T., Valentino L., Desmopressin (DDAVP) in the management of patients with congenital bleeding disorders, 10.1111/hae.12254
- Makris, Throb Res, 127, S22 (2010)
Bibliographic reference | Windyga, Jerzy ; Dolan, Gerry ; Altisent, Carme ; Katsarou, Olga ; López-Fernández, María Fernanda ; et. al. Practical aspects of DDAVP use in patients with von Willebrand Disease undergoing invasive procedures: a European survey.. In: Haemophilia : the official journal of the World Federation of Hemophilia, Vol. 22, no.1, p. 110-120 (2016) |
---|---|
Permanent URL | http://hdl.handle.net/2078.1/208408 |