Von Willebrand Disease Minimize Menorrhagia (VWDMin) Trial
نویسندگان
چکیده
منابع مشابه
screening of von willebrand disease in iranian women with menorrhagia
conclusions the high prevalence of vwd among our patients was the same as other previous reports, suggesting low awareness about this disease and under diagnosis of mild cases. results mean age of our patients was 32.5 ± 10.6 years. the level of von willebrand factor in 22.5% and von willebrand activity in 19.6% of patients was abnormal. the prevalence of vwd among patients with menorrhagia was...
متن کاملScreening of Von Willebrand Disease in Iranian Women With Menorrhagia
BACKGROUND Menorrhagia is a common health problem in women, particularly those with bleeding disorders. Little is known about the course of menorrhagia or other bleeding symptoms in women with the most common congenital bleeding disorder, von Willebrand disease (vWD). OBJECTIVES The aim of this study was to estimate the prevalence of vWD in women with diagnosed menorrhagia. MATERIALS AND ME...
متن کاملPhase II prospective open-label trial of recombinant interleukin-11 in women with mild von Willebrand disease and refractory menorrhagia.
Lack of effective treatment for menorrhagia is the greatest unmet healthcare need in women with von Willebrand disease (VWD). We conducted a single-centre phase II clinical trial to determine efficacy and safety of recombinant IL-11 (rhIL-11, Neumega®) given subcutaneously for up to seven days during six consecutive menstrual cycles each in seven women with mild VWD and menorrhagia refractory t...
متن کاملDefining von Willebrand disease.
for repeat testing. The authors’ conclusion that it should be considered for screening patients requires further consideration and study but conceivably, this assay should improve the future of VWD diagnosis. Conflict-of-interest disclosure: P.D.J. has received research funding from Bayer, CSL Behring, and Octapharma; and honoraria for educational talks from Baxalta, CSL Behring, and Octapharma. n
متن کاملVon Willebrand disease
hereditary elliptocytosis and hereditary pyropoikilocytosis. Blood Cells Mol Dis 1996;22:254–8. 8 Delaunay J. The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations. Semin Hematol 2004;41:165–72. 9 Carella M, Stewart G, Ajetunmobi JF et al. Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Blood
سال: 2019
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood-2019-124234