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Volumn 17, Issue 5, 2011, Pages 441-448

An evaluation of the DDAVP infusion test with PFA-100 and vWF activity assays to distinguish vWD types in children

Author keywords

DDAVP; PFA 100; von Willebrand disease (vWD); von Willebrand factor (vWF)

Indexed keywords

BLOOD CLOTTING FACTOR 8; DESMOPRESSIN; RISTOCETIN; VON WILLEBRAND FACTOR;

EID: 80053605263     PISSN: 10760296     EISSN: 19382723     Source Type: Journal    
DOI: 10.1177/1076029610366440     Document Type: Article
Times cited : (8)

References (31)
  • 1
    • 0029084031 scopus 로고
    • Laboratory assessment of von Willebrand factor: Use of different assays can influence the diagnosis of von Willebrand's disease, depending on differing sensitivity to sample preparation and differential recognition of high molecular weight VWF forms
    • Favaloro EJ, Facey D, Grispo L. Laboratory assessment of Von Willebrand factor: use of different assays can influence the diagnosis of Von Willebrand's disease, depending on differing sensitivity to sample preparation and differential recognition of high molecular weight VWF forms. Am J Clin Pathol. 1995 ; 104 (3). 264-271
    • (1995) Am J Clin Pathol , vol.104 , Issue.3 , pp. 264-271
    • Favaloro, E.J.1    Facey, D.2    Grispo, L.3
  • 4
    • 0035081481 scopus 로고    scopus 로고
    • Laboratory diagnosis of von Willebrand disorder (vWD) and monitoring of DDAVP therapy: Efficacy of the PFA-100® and vWF:CBA as combined diagnostic strategies
    • DOI 10.1046/j.1365-2516.2001.00487.x
    • Favaloro EJ, Kershaw G, Bukuya M, Hertzberg M, Koutts J. Laboratory diagnosis of Von Willebrand Disorder (VWD) and monitoring of DDAVP therapy: efficacy of the PFA-100 and VWF:CBA as combined diagnostic strategies. Haemophilia. 2001 ; 7 (2). 180-189 (Pubitemid 32243801)
    • (2001) Haemophilia , vol.7 , Issue.2 , pp. 180-189
    • Favaloro, E.J.1    Kershaw, G.2    Bukuya, M.3    Hertzberg, M.4    Koutts, J.5
  • 5
    • 0028201807 scopus 로고
    • A revised classification of von Willebrand disease. for the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
    • Sadler EJ. A revised classification of Von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost. 1994 ; 71 (4). 520-525
    • (1994) Thromb Haemost , vol.71 , Issue.4 , pp. 520-525
    • Sadler, E.J.1
  • 8
    • 0036236926 scopus 로고    scopus 로고
    • Response of von Willebrand factor parameters to desmopressin in patients with type 1 and type 2 congenital von Willebrand disease: Diagnostic and therapeutic implications
    • DOI 10.1055/s-2002-27814
    • Michiels JJ, van de Velde A, van Vliet HHDM, van der Planken M, Schroyens W, Berneman Z. Response of von Willebrand factor parameters to desmopressin in patients with type 1 and type 2 congenital von Willebrand disease: diagnostic and therapeutic implications. Semin Thromb Hemost. 2002 ; 28 (2). 111-131 (Pubitemid 34439202)
    • (2002) Seminars in Thrombosis and Hemostasis , vol.28 , Issue.2 , pp. 111-131
    • Michiels, J.J.1    Van De Velde, A.2    Van Vliet, H.H.D.M.3    Van Der Planken, M.4    Schroyens, W.5    Berneman, Z.6
  • 10
    • 33644977050 scopus 로고    scopus 로고
    • A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1 VWD)
    • Tosetto A, Rodeghiero F, Castaman G, et al. A quantitative analysis of bleeding symptoms in type 1 Von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost. 2006 ; 4 (4). 766-773
    • (2006) J Thromb Haemost , vol.4 , Issue.4 , pp. 766-773
    • Tosetto, A.1    Rodeghiero, F.2    Castaman, G.3
  • 11
    • 33746602713 scopus 로고    scopus 로고
    • Laboratory identification of von Willebrand disease: Technical and scientific perspectives
    • DOI 10.1055/s-2006-947859
    • Favaloro EJ. Laboratory identification of Von Willebrand Disease: technical and scientific perspectives. Semin Thromb Hemost. 2006 ; 32 (5). 456-471 (Pubitemid 44157383)
    • (2006) Seminars in Thrombosis and Hemostasis , vol.32 , Issue.5 , pp. 456-471
    • Favaloro, E.J.1
  • 13
    • 12344262502 scopus 로고    scopus 로고
    • Phenotypic and genotypic diagnosis of von Willebrand disease: A 2004 update
    • DOI 10.1053/j.seminhematol.2004.10.002, PII S0037196304002501, von Willebrand Factor in Hemostasis and Thrombosis
    • Schneppenheim R, Budde U. Phenotypic and genotypic diagnosis of Von Willebrand disease: a 2004 update. Semin Hematol. 2005 ; 42 (1). 15-28 (Pubitemid 40127266)
    • (2005) Seminars in Hematology , vol.42 , Issue.1 , pp. 15-28
    • Schneppenheim, R.1    Budde, U.2
  • 15
    • 33746650150 scopus 로고    scopus 로고
    • The utility of the PFA-100 in the identification of von Willebrand disease: A concise review
    • DOI 10.1055/s-2006-947869
    • Favaloro EJ. The utility of the PFA-100 in identification of Von Willebrand Disease: a concise review. Semin. Thromb Hemost. 2006 ; 32 (5). 537-545 (Pubitemid 44157393)
    • (2006) Seminars in Thrombosis and Hemostasis , vol.32 , Issue.5 , pp. 537-545
    • Favaloro, E.J.1
  • 17
    • 0345581410 scopus 로고    scopus 로고
    • Comparison of PFA-100 closure time and template bleeding time of patients with inherited disorders causing defective platelet function
    • Kerenyi A, Schlammadinger A, Ajzner E, et al. Comparison of PFA-100 closure time and template bleeding time of patients with inherited disorders causing defective platelet function. Thromb Res. 1999 ; 96 (6). 487-492
    • (1999) Thromb Res , vol.96 , Issue.6 , pp. 487-492
    • Kerenyi, A.1    Schlammadinger, A.2    Ajzner, E.3
  • 18
    • 0033935043 scopus 로고    scopus 로고
    • Comparison of the O'Brien filter test and the PFA-100 platelet analyzer in the laboratory diagnosis of von Willebrand's disease
    • Schlammadinger A, Kerenyi A, Muszbek L, Boda Z. Comparison of the O'Brien filter test and the PFA-100 platelet analyser in the laboratory diagnosis of Von Willebrand's disease. Thromb Haemost. 2000 ; 84 (1). 88-92 (Pubitemid 30433674)
    • (2000) Thrombosis and Haemostasis , vol.84 , Issue.1 , pp. 88-92
    • Schlammadinger, A.1    Kerenyi, A.2    Muszbek, L.3    Boda, Z.4
  • 19
    • 19944374427 scopus 로고    scopus 로고
    • Laboratory aspects of diagnosis and treatment
    • Favaloro EJ, Lillicrap D, Lazzari MA, et al. Laboratory aspects of diagnosis and treatment. Haemophilia. 2004 ; 10 (suppl 4). 164-168
    • (2004) Haemophilia , vol.10 , Issue.SUPPL. 4 , pp. 164-168
    • Favaloro, E.J.1    Lillicrap, D.2    Lazzari, M.A.3
  • 21
    • 29244478621 scopus 로고    scopus 로고
    • Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype
    • DOI 10.1111/j.1538-7836.2005.01631.x
    • Lanke E, Johansson AM, Halldén C, Lethagen S. Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype. J Thromb Haemost. 2005 ; 3 (12). 2656-2663 (Pubitemid 41819792)
    • (2005) Journal of Thrombosis and Haemostasis , vol.3 , Issue.12 , pp. 2656-2663
    • Lanke, E.1    Johansson, A.M.2    Hallden, C.3    Lethagen, S.4
  • 22
    • 33748751277 scopus 로고    scopus 로고
    • Characterization of recessive severe type 1 and 3 von willebrand disease (vwd), asymptomatic heterozygous carriers versus bloodgroup o-related von willebrand factor deficiency, and dominant type 1 VWD
    • DOI 10.1177/1076029606291401
    • Michiels JJ, Berneman Z, Gadisseur A, et al. Characterization of recessive severe type 1 and 3 Von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related Von Willebrand factor deficiency, and dominant type 1 VWD. Clin Appl Thromb Hemost. 2006 ; 12 (3). 277-295 (Pubitemid 44400839)
    • (2006) Clinical and Applied Thrombosis/Hemostasis , vol.12 , Issue.3 , pp. 277-295
    • Michiels, J.J.1    Berneman, Z.2    Gadisseur, A.3    Van Der Planken, M.4    Schroyens, W.5    Van De Velde, A.6    Van Vliet, H.7
  • 23
    • 0025236609 scopus 로고
    • Luminographic detection of von Willebrand factor multimers in agarose gels and on nitrocellulose membranes
    • Budde U, Schneppenheim R, Plendl H, Dent J, Ruggeri ZM, Zimmerman TS. Luminographic detection of Von Willebrand factor multimers in agarose gels and on nitrocellulose membranes. Thromb Haemost. 1990 ; 63 (2). 312-315 (Pubitemid 20128202)
    • (1990) Thrombosis and Haemostasis , vol.63 , Issue.2 , pp. 312-315
    • Budde, U.1    Schneppenheim, R.2    Plendl, H.3    Dent, J.4    Ruggeri, Z.M.5    Zimmerman, T.S.6
  • 24
    • 33644979514 scopus 로고    scopus 로고
    • Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
    • Eikenboom J, Van Marion V, Putter H, et al. Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD. J Thromb Haemost. 2006 ; 4 (4). 774-782
    • (2006) J Thromb Haemost , vol.4 , Issue.4 , pp. 774-782
    • Eikenboom, J.1    Van Marion, V.2    Putter, H.3
  • 25
    • 55549101968 scopus 로고    scopus 로고
    • Major haemorrhage related to surgery in patients with type 1 and possible type 1 von Willebrand disease
    • Woods AI, Blanco AN, 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
    • (2008) Thromb Haemost , vol.100 , Issue.5 , pp. 797-802
    • Woods, A.I.1    Blanco, A.N.2    Chuit, R.3
  • 26
    • 51349134516 scopus 로고    scopus 로고
    • PFA-100 monitoring of von Willebrand factor (VWF) responses to DDAVP and FVIII/VWF concentrate in von Willebrand disease type 1 and 2
    • Van Vliet HHDM, Kappers-Klunne MC, Leebeek F, Michiels JJ. PFA-100 monitoring of von Willebrand factor (VWF) responses to DDAVP and FVIII/VWF concentrate in von Willebrand disease type 1 and 2. Thromb Haemost. 2008 ; 100 (3). 462-468
    • (2008) Thromb Haemost , vol.100 , Issue.3 , pp. 462-468
    • Van Vliet, H.H.D.M.1    Kappers-Klunne, M.C.2    Leebeek, F.3    Michiels, J.J.4
  • 27
    • 51349090488 scopus 로고    scopus 로고
    • A better approach to monitoring of therapy in von Willebrand disease?
    • Favaloro EJ. A better approach to monitoring of therapy in von Willebrand disease?. Thromb Haemost. 2008 ; 100 (3). 371-373
    • (2008) Thromb Haemost , vol.100 , Issue.3 , pp. 371-373
    • Favaloro, E.J.1
  • 28
    • 43949141204 scopus 로고    scopus 로고
    • Survival of von Willebrand factor released following DDAVP in a type I von Willebrand disease cohort: Influence of glycosylation, proteolysis and gene mutations
    • DOI 10.1160/TH07-09-0565
    • Millar CM, Riddell AF, Brown SA, et al. Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: influence of glycolysation, proteolysis and gene mutations. Thromb Haemost. 2008 ; 99 (5). 916-924 (Pubitemid 351705309)
    • (2008) Thrombosis and Haemostasis , vol.99 , Issue.5 , pp. 916-924
    • Millar, C.M.1    Riddell, A.F.2    Brown, S.A.3    Starke, R.4    Mackie, I.5    Bowen, D.J.6    Jenkins, P.V.7    Van Mourik, J.A.8
  • 30
    • 0033790284 scopus 로고    scopus 로고
    • Von Willebrand factor ristocetin cofactor activity correlates with platelet function in a high shear stress system
    • Veyradier A, Fressinaud E, Boyer-Neumann C, Trossaert M, Meyer D. von Willebrand factor ristocetin cofactor activity correlates with platelet function in a high shear stress system. Thromb Haemost. 2000 ; 84 (4). 727-728
    • (2000) Thromb Haemost , vol.84 , Issue.4 , pp. 727-728
    • Veyradier, A.1    Fressinaud, E.2    Boyer-Neumann, C.3    Trossaert, M.4    Meyer, D.5
  • 31
    • 34547890673 scopus 로고    scopus 로고
    • 2B or not 2B? Disparate discrimination of functional VWF discordance using different assay panels or methodologies may lead to success or failure in the early identification of type 2B VWD
    • DOI 10.1160/TH06-12-0693
    • Favaloro EJ, Bonar R, Meiring M, Street A, Marsden K. RCPA QAP in Haematology. 2B or not 2B? Disparate discrimination of functional VWF discordance using different assay panels or methodologies may lead to success or failure in the early identification of type 2B VWD. Thromb Haemost. 2007 ; 98 (2). 346-358 (Pubitemid 47250238)
    • (2007) Thrombosis and Haemostasis , vol.98 , Issue.2 , pp. 346-358
    • Favaloro, E.J.1    Bonar, R.2    Meiring, M.3    Street, A.4    Marsden, K.5


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