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Chapter 19 - Management of Inherited Disorders of Primary Hemostasis in Pregnancy

from Section 7 - Hemorrhagic Disorders

Published online by Cambridge University Press:  01 February 2018

By
Sue Pavord  and
Carolyn Millar
Edited by
Sue Pavord  and
Beverley Hunt
Sue Pavord
Affiliation:
University of Oxford
Beverley Hunt
Affiliation:
King's College London
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The Obstetric Hematology Manual , pp. 233 - 245
Publisher: Cambridge University Press
Print publication year: 2018

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References

Pavord, S, Rayment, R, Madan, B et al. The Management of Inherited Bleeding Disorders in Pregnancy. RCOG Green-Top Guideline No. 71; 2017. http://onlinelibrary.wiley.com/doi/10.1111/1471-0528.14592/epdfGoogle Scholar
Abildgaard, CF, Suzuki, Z, Harrison, J et al. Serial studies in von Willebrand’s disease: variability versus “variants”. Blood 1980; 56(4): 712–716.Google Scholar
Sadler, JE, Budde, U, Eikenboom, JC et al. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. Journal of Thrombosis and Haemostasis 2006; 4(10): 2103–2114.CrossRefGoogle ScholarPubMed
Rydz, N, James, PD. The evolution and value of bleeding assessment tools. Journal of Thrombosis and Haemostasis 2012; 10(11): 2223–2229.Google Scholar
Rodeghiero, F, Tosetto, A, Abshire, T et al. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders. Journal of Thrombosis and Haemostasis 2010; 8(9): 2063–2065.CrossRefGoogle Scholar
Laffan, MA, Lester, W, O’Donnell, JS et al. The diagnosis and management of von Willebrand disease: a United Kingdom Hemophilia Center Doctors Organization guideline approved by the British Committee for Standards in Hematology. British Journal of Haematology 2014; 167(4): 453–465.CrossRefGoogle Scholar
James, PD, Paterson, AD, Notley, C et al. Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study. Journal of Thrombosis and Haemostasis 2006; 4(4): 783–792.Google Scholar
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. Journal of Thrombosis and Haemostasis 2006; 4(4): 774–782.Google Scholar
Stirling, Y, Woolf, L, North, WR et al. Hemostasis in normal pregnancy. Thrombosis and Haemostasis 1984; 52(2): 176–182.Google ScholarPubMed
Sanchez-Luceros, A, Meschengieser, SS, Marchese, C et al. Factor VIII and von Willebrand factor changes during normal pregnancy and puerperium. Blood Coagulation and Fibrinolysis 2003; 14: 647–651.Google Scholar
Ranger, A, Manning, RA, Lyall, H et al. Pregnancy in type 2B VWD: a case series. Hemophilia 2012; 18(3): 406–412.Google Scholar
James, AH, Jamison, MG. Bleeding events and other complications during pregnancy and childbirth in women with von Willebrand disease. Journal of Thrombosis and Haemostasis 2007; 5: 1165–1169.CrossRefGoogle ScholarPubMed
Ray, JG. DDAVP use during pregnancy: an analysis of its safety for mother and child. Obstetrical & Gynecological Survey 1998; 53(7): 450–455.Google Scholar
Trigg, DE, Stergiotou, I, Peitsidis, P et al. A systematic review: The use of desmopressin for treatment and prophylaxis of bleeding disorders in pregnancy. Hemophilia 2012; 18(1): 25–33.Google Scholar
Mannucci, PM, Tenconi, PM, Castaman, G, Rodeghiero, F. Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trial. Blood 1992; 79: 3130–3137.CrossRefGoogle ScholarPubMed
Huq, FY, Kulkarni, A, Agbim, EC et al. Changes in the levels of factor VIII and von Willebrand factor in the puerperium. Hemophilia 2012; 18: 241–245.CrossRefGoogle ScholarPubMed
Roqué, H, Funai, E, Lockwood, CJ. von Willebrand disease and pregnancy. The Journal of Maternal–Fetal Medicine 2000; 9: 257–266.Google ScholarPubMed
Lentaigne, CE, Sodhi, V, Usman, N, McCarthy, A, Millar, CM. Hemostatic management of pregnant women with platelet function disorders: utility of PFA-100. Journal of Thrombosis and Haemostasis 2013; 11: 1152.Google Scholar

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