Diagnosis and management of von Willebrand disease in a single institution of Argentina

Seminars in Thrombosis and Hemostasis

Volumn 37, Issue 5, 2011, Pages 568-575

  Woods, Adriana I ^a,b   Sánchez Luceros, Analía ^a,b   Meschengieser, Susana S ^a   Kempfer, Ana C ^a,b   Blanco, Alicia N ^a   Lazzari, María A ^a,b  

^a INST DE INVEST HEMATOLOGICAS   (Argentina)

^b Facultad de Ciencias Naturales e Instituto M Lillo   (Argentina)

Author keywords

DDAVP in women and children; genotype phenotype relationships; management strategy; prophylaxis in VWD; von Willebrand disease

Indexed keywords

BLOOD CLOTTING FACTOR 8; DESMOPRESSIN; HORMONE; RECOMBINANT BLOOD CLOTTING FACTOR 7A; THROMBOCYTE CONCENTRATE;

ARGENTINA; ARTICLE; BLEEDING; BLOOD GROUP O; BLOOD TRANSFUSION; CLINICAL FEATURE; CRYOPRECIPITATE; DEVELOPING COUNTRY; DIAGNOSTIC TEST; DISEASE SEVERITY; DRUG EFFICACY; DRUG SAFETY; ECCHYMOSIS; EPISTAXIS; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HEMATOMA; HUMAN; LABORATORY TEST; LONG TERM CARE; MENORRHAGIA; OBSTETRICS; PEDIATRICIAN; PHENOTYPE; PREGNANCY; PRIORITY JOURNAL; TREATMENT RESPONSE; VON WILLEBRAND DISEASE;

ADOLESCENT; ADULT; ARGENTINA; CHILD; CHILD, PRESCHOOL; DEAMINO ARGININE VASOPRESSIN; FEMALE; GENETIC ASSOCIATION STUDIES; HEMOSTATICS; HUMANS; MALE; MIDDLE AGED; MUTATION; PREGNANCY; TREATMENT OUTCOME; VON WILLEBRAND DISEASES; VON WILLEBRAND FACTOR; YOUNG ADULT;

EID: 81755171926     PISSN: 00946176     EISSN: 10989064     Source Type: Journal    
DOI: 10.1055/s-0031-1281044     Document Type: Article

References (23)

1. Srivastava A. von Willebrand disease in the developing world. Semin Hematol 2005 42 1 36-41 (Pubitemid 40127268)
2. Miller C H., Graham J B., Goldin L R., Elston R C. Genetics of classic von Willebrand's disease. I. Phenotypic variation within families. Blood 1979 54 1 117-136 (Pubitemid 9228092)
3. International Society on Thrombosis and Haematosis. SSC minutes. Available at: http://www.isth.org/default/index.cfm/publications/ssc-minutes/ Accessed October 2010
4. Woods A I., Keller L, Kempfer A C., Farias C R., Casais P, Lazzari M A. CSGE to scan the exon 22 of von Willebrand factor gene for diagnosing von Willebrand disease 2N. Pathophysiol Haemost Thromb 2006 35 12 28 Abstract 1058
5. Nichols W L., Hultin M B., James A H. et al. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008 14 2 171-232 (Pubitemid 351343618)
6. Woods A I., Meschengieser S S., Blanco A N. et al. Clinical features and laboratory patterns in a cohort of consecutive Argentinian patients with von Willebrand's disease. Haematologica 2001 86 4 420-427 (Pubitemid 32428504)
7. Federici A B., Mannucci P M., Castaman G et al. Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients. Blood 2009 113 3 526-534
8. Nitu-Whalley I C., Lee C A., Griffioen A, Jenkins P V., Pasi K J. Type 1 von Willebrand diseasea clinical retrospective study of the diagnosis, the influence of the ABO blood group and the role of the bleeding history. Br J Haematol 2000 108 2 259-264 (Pubitemid 30143638)
9. Onundarson P T., Gudmundsdottir B R., Arnfinnsdottir A V., Kjeld M, Olafsson O. von Willebrand factor does not vary during normal menstrual cycle. Thromb Haemost 2001 85 1 183-184 (Pubitemid 32050964)
10. Meschengieser S S., Alberto M F., Salviú J, Bermejo E, Lazzari M A. Recurrent haemoperitoneum in a mild von Willebrand's disease combined with a storage pool deficit. Blood Coagul Fibrinolysis 2001 12 3 207-209 (Pubitemid 32525458)
11. Favaloro E J., Lillicrap D, Lazzari M A. et al. von Willebrand disease: laboratory aspects of diagnosis and treatment. Haemophilia 2004 10 Suppl 4 164-168 (Pubitemid 40045437)
12. Casais P, Carballo G A., Woods A I. et al. R924Q substitution encoded within exon 21 of the von Willebrand factor gene related to mild bleeding phenotype. Thromb Haemost 2006 96 2 228-230 (Pubitemid 44219393)
13. Woods A I., Kempfer A C, Keller L, Calderazzo J C., Sánchez- Luceros A, Paiva-Palomino J, Lazzari MA. Genotypic diagnosis of VWD: preliminary results in the analysis of exon 28. J Thromb Haemost 2009 7 Suppl 2 Abstract 610
14. Woods A I., Blanco A N., Chuit R et al. Major haemorrhage related to surgery in patients with type 1 and possible type 1 von Willebrand disease. Thromb Haemost 2008 100 5 797-802
15. Castaman G, Montgomery R R., Meschengieser S S., Haberichter S L., Woods A I., Lazzari M A. von Willebrand's disease diagnosis and laboratory issues. Haemophilia 2010 16 Suppl 5 67-73
16. Sánchez-Luceros A, Meschengieser S S., Marchese C et al. Factor VIII and von Willebrand factor changes during normal pregnancy and puerperium. Blood Coagul Fibrinolysis 2003 14 7 647-651 (Pubitemid 37323742)
17. Noller K L., Bowie E J., Kempers R D., Owen C A. Jr. von Willebrand's disease in pregnancy. Obstet Gynecol 1973 41 6 865-872
18. Kadir R A., Lee C A., Sabin C A., Pollard D, Economides D L. Pregnancy in women with von Willebrand's disease or factor XI deficiency. Br J Obstet Gynaecol 1998 105 3 314-321 (Pubitemid 28123582)
19. Mannucci P M. Use of desmopressin (DDAVP) during early pregnancy in factor VIII-deficient women. Blood 2005 105 8 3382
20. Sánchez-Luceros A, Meschengieser S S., Turdó K et al. Evaluation of the clinical safety of desmopressin during pregnancy in women with a low plasmatic von Willebrand factor level and bleeding history. Thromb Res 2007 120 3 387-390 (Pubitemid 46879897)
21. Sánchez-Luceros A, Meschengieser S S., Woods A I. et al. Biological and clinical response to desmopressin (DDAVP) in a retrospective cohort study of children with low von Willebrand factor levels and bleeding history. Thromb Haemost 2010 104 5 984-989
22. Sánchez-Luceros A, Woods A I., Meschengieser S S., Grosso S, Lazzari M A. Factor VIII and von Willebrand activity are strongly related to the desmopressin biological response in von Willebrand disease. J Thromb Haemost 2009 7 Suppl 2 Abstract 613
23. Berntorp E, de Moerloose P, Ljung R C. The role of prophylaxis in bleeding disorders. Haemophilia 2010 16 Suppl 5 189-193