Patients with von Willebrand disease in China: Results of an online survey

被引:3
作者
Yang, Wen [1 ]
Bi, Hui [1 ]
Wang, Xiuli [1 ]
Yang, Zhichun [2 ]
Wang, Yacan [1 ]
Tan, Yaxian [1 ]
Wang, Honghui [1 ]
Xie, Dongmei [1 ]
Mu, Hongli [1 ]
Yin, Lingmei [1 ]
Zhou, Zeping [1 ]
机构
[1] Kunming Med Univ, Dept Hematol, Affiliated Hosp 2, Kunming, Yunnan, Peoples R China
[2] Kunming Med Univ, Dept Resp & Crit Care Med, Affiliated Hosp 2, Kunming, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
China; online survey; Von Willebrand disease; DIAGNOSIS; MANAGEMENT; BLEEDINGS; MODERATE; CHILDREN;
D O I
10.1111/hae.14671
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Little is known about the clinical characteristics of von Willebrand disease (VWD) patients in China, the impact of Covid-19 on them and their genetic mutation. Aim To describe the clinical characteristics of a group of VWD patients in China, the impact of Covid-19 on them and their genetic mutation. Methods An online survey using a self-designed questionnaire was conducted among patients within a WeChat group of VWD patients in China. Data were analysed using t-test, the Chi-square test, Fisher's exact test and rank sum test. Results Data from a total of 96 patients were collected. Several important findings are yielded. Above all, type 3 patients accounted for over half of the surveyed patients. Secondly, a surprising rate (>40%) of patients had experience of being misdiagnosed. Thirdly, treatment regimens were dominated by cryoprecipitate, blood-derived FVIII and plasma, and only a small percentage of patients received prophylaxis. Fourthly, we identified 17 new von Willebrand factor (VWF) mutant genes which merit further investigation. Additionally, Covid-19 was found to pose some challenges for the patients. Conclusion In China, the high rates of type 3 patients and misdiagnosis suggest that most of the VWD patients may never be diagnosed in China. When it comes to diagnosis and treatment, there is a large gap between developing countries like China and developed countries.
引用
收藏
页码:230 / 239
页数:10
相关论文
共 17 条
  • [1] Higher rates of bleeding and use of treatment products among young boys compared to girls with von Willebrand disease
    Abe, Karon
    Dupervil, Brandi
    O'Brien, Sarah H.
    Oakley, Meredith
    Kulkarni, Roshni
    Gill, Joan Cox
    Byams, Vanessa
    Soucie, Michael J.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2020, 95 (01) : 10 - 17
  • [2] Diagnosis and Management of von Willebrand Disease in Spain
    Batlle, Javier
    Perez-Rodriguez, Almudena
    Costa Pinto, Joana
    Loures Fraga, Esther
    Rodriguez-Trillo, Angela
    Fernanda Lopez-Fernandez, Maria
    [J]. SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2011, 37 (05) : 503 - 510
  • [3] Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate®, a new generation von Willebrand factor/factor VIII concentrate
    Berntorp, E.
    Windyga, J.
    [J]. HAEMOPHILIA, 2009, 15 (01) : 122 - 130
  • [4] Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire
    Biss, T. T.
    Blanchette, V. S.
    Clark, D. S.
    Bowman, M.
    Wakefield, C. D.
    Silva, M.
    Lillicrap, D.
    James, P. D.
    Rand, M. L.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (05) : 950 - 956
  • [5] The prevalence of symptomatic von Willebrand disease in primary care practice
    Bowman, M.
    Hopman, W. M.
    Rapson, D.
    Lillicrap, D.
    James, P.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (01) : 213 - 216
  • [6] Principles of care for the diagnosis and treatment of von Willebrand disease
    Castaman, Giancarlo
    Goodeve, Anne
    Eikenboom, Jeroen
    [J]. HAEMATOLOGICA, 2013, 98 (05) : 667 - 674
  • [7] Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease
    de Wee, Eva M.
    Sanders, Yvonne V.
    Mauser-Bunschoten, Eveline P.
    van der Bom, Johanna G.
    Degenaar-Dujardin, Manon E. L.
    Eikenboom, Jeroen
    de Goede-Bolder, Arja
    Laros-van Gorkom, Britta A. P.
    Meijer, Karina
    Hamulyak, Karly
    Nijziel, Marten R.
    Fijnvandraat, Karin
    Leebeek, Frank W. G.
    [J]. THROMBOSIS AND HAEMOSTASIS, 2012, 108 (04) : 683 - 692
  • [8] Characteristics, complications, and sites of bleeding among infants and toddlers less than 2 years of age with VWD
    Dupervil, Brandi
    Abe, Karon
    O'Brien, Sarah H.
    Oakley, Meredith
    Kulkarni, Roshni
    Thornburg, Courtney D.
    Byams, Vanessa R.
    Soucie, J. Michael
    [J]. BLOOD ADVANCES, 2021, 5 (08) : 2079 - 2086
  • [9] Management of Inherited von Willebrand Disease in Italy: Results from the Retrospective Study on 1234 Patients
    Federici, Augusto B.
    Bucciarelli, Paolo
    Castaman, Giancarlo
    Baronciani, Luciano
    Canciani, Maria T.
    Mazzucconi, Maria G.
    Morfini, Massimo
    Rocino, Angiola
    Schiavoni, Mario
    Oliovecchio, Emily
    Iorio, Alfonso
    Mannucci, Pier M.
    [J]. SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2011, 37 (05) : 511 - 521
  • [10] 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
    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
    [J]. CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 2007, 13 (01) : 14 - 34