The Hemophilia Utilization Group Study (HUGS): a retrospective assessment of health status of persons with haemophilia

被引:0
|
作者
Globe, D [1 ]
机构
[1] Univ So Calif, Los Angeles, CA 90089 USA
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:47 / 47
页数:1
相关论文
共 50 条
  • [21] LONGITUDINAL CHANGES IN HEALTH-RELATED QUALITY OF LIFE FOR CHRONIC DISEASES: AN EXAMPLE FROM THE HEMOPHILIA UTILIZATION GROUP STUDY PART VA (HUGS VA)
    Poon, J. L.
    Doctor, J.
    Gwadry-Sridhar, F.
    Ullman, M.
    Riske, B.
    Baker, J.
    Niu, X.
    Lou, M.
    Nichol, M. B.
    VALUE IN HEALTH, 2013, 16 (03) : A122 - A123
  • [22] The association of barriers to care and health related quality of life in patients with factor VIII deficiency - The hemophilia utilization group study - Part V (HUGS-V)
    Wu, J.
    Globe, D.
    Gwadry-Sridhar, F.
    Forsberg, A.
    Riske, B.
    Johnson, K. A.
    VALUE IN HEALTH, 2007, 10 (03) : A155 - A155
  • [23] The hemophilia utilization group study.
    Globe, D
    Kominski, G
    Curtis, R
    Dietrich, S
    Sanders, N
    Miller, R
    Parish, K
    TRANSFUSION, 1997, 37 (05) : 540 - 541
  • [24] Health Status of Elderly Persons with Hemophilia Compared with the General Population: The Sphera Study
    Marchesini, E.
    Iorio, A.
    Coppola, A.
    Santagostino, E.
    Tagariello, G.
    Castaman, G.
    Valdre, L.
    Santoro, C.
    Rivolta, G. F.
    Ettorre, C.
    Zanon, E.
    Barillari, G.
    Cantori, I.
    Caimi, T. M.
    Latella, C.
    Oliovecchio, E.
    Mannucci, M.
    HAEMOPHILIA, 2016, 22 : 29 - 30
  • [25] Measuring parental work absence associated with factor concentrate administration in children with hemophilia in the United States: Hemophilia Utilization Group Study Part V (HUGS V)
    Niu, Xiaoli
    Riske, Brenda
    Ullman, Megan
    Poon, Jiat Ling
    Lou, Mimi
    Baker, Judith
    Parish, Kathy L.
    Kulkarni, Roshni
    Curtis, Randall
    Nichol, Michael B.
    HAEMOPHILIA, 2014, 20 : 140 - 140
  • [26] Haemophilia utilization group study (HUGS V): summary of baseline data-demographics, clinical characteristics, barriers to care, arthropathy and quality of life
    Zheng, Y. Z.
    Baker, J. R.
    Globe, D. R.
    Riske, B.
    Ann, D.
    Joanne, W. U.
    Ullman, Megan M.
    Duncan, Natalie
    Smith, C.
    Gwadry-Sridhar, F.
    Curtis, Randall G.
    Koerper, M. A.
    Parish, Kathy L.
    Johnson, K. A.
    HAEMOPHILIA, 2008, 14 (04) : 876 - 876
  • [27] Factors associated with lower health-related quality of life (HRQOL) in adults with factor VIII deficiency - The hemophilia utilization group study-part V (HUGS-V)
    Zhou, Z. Y.
    Wu, J.
    Globe, D.
    Gwadry-Sridhar, F.
    Riske, B.
    Ullman, M.
    Huszti, H.
    Koerper, M.
    Baker, J.
    Johnson, K. A.
    VALUE IN HEALTH, 2008, 11 (03) : A163 - A164
  • [28] Psychosocial assessment and need based intervention program for persons with hemophilia of the Haemophilia Society Calcutta Chapter
    Mitra, A.
    Basu, J.
    Kar, S.
    HAEMOPHILIA, 2008, 14 : 146 - 146
  • [29] Joint health status of Chinese hemophilia children: a pilot study using the Hemophilia Joint Health Assessment Scale (HJHS)
    Chen, L.
    Sun, J.
    Wu, R.
    Luke, K.
    Poon, M.
    Hang, M.
    Hillard, P.
    Feldman, B.
    Blanchette, V.
    HAEMOPHILIA, 2008, 14 : 79 - 79
  • [30] The impact of haemophilia on the social status and the health-related quality of life in adult Lebanese persons with haemophilia
    Naous, Elie
    de Moerloose, Philippe
    Sleilaty, Ghassan
    Casini, Alessandro
    Khayat, Claudia Djambas
    HAEMOPHILIA, 2019, 25 (02) : 264 - 269