Carrier testing and prenatal diagnosis of haemophilia - utilisation and psychological consequences

被引:9
作者
Tedgard, U [1 ]
机构
[1] Malmo Univ Hosp, Univ Lund, Dept Paediat, S-20502 Malmo, Sweden
[2] Malmo Univ Hosp, Univ Lund, Dept Coagulat Disorders, Malmo, Sweden
关键词
haemophilia; carrier testing; prenatal diagnosis; risk factors; psychology;
D O I
10.1046/j.1365-2516.1998.440365.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Attitudes towards prenatal diagnosis, and abortion vary widely between different countries, religions, cultures and over time. Carrier testing and prenatal diagnosis (PD) of haemophilia have become an integrated pan: of the comprehensive care for haemophilia in Sweden as well as in many other countries. Almost all carriers are interested in carrier testing if they are aware of the possibility. With the development of PD by chorionic villus sampling in the first trimester, the method became acceptable for many carriers, and it has in Sweden actually had an effect on the incidence of haemophilia in the 1990s. The use of PD is more common among women who perceive haemophilia as a very serious disease and who have a positive attitude towards legal abortion. The main reason for carriers not to use PD was that they do not find haemophilia to be a sufficiently serious disorder to justify an abortion. Women and their spouses are under a great deal of psychological pressure in association with the PD procedure, and the psychological consequences of having to terminate a pregnancy are long-lasting. At follow-up, about 6 years after PD and abortion, these women, however, do not have more signs of psychological distress than women without PD experience. Nevertheless, they must be offered qualified assistance both before and after PD as well as adequate follow-up after an abortion to help them cope with the emotional strain they are under.
引用
收藏
页码:365 / 369
页数:5
相关论文
共 50 条
  • [41] Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease
    Schleutker, J
    Sistonen, P
    Aula, P
    JOURNAL OF MEDICAL GENETICS, 1996, 33 (01) : 36 - 41
  • [42] PRENATAL-DIAGNOSIS AND CARRIER DETECTION IN FRAGILE-X
    VONKOSKULL, H
    NORDSTROM, AM
    SALONEN, R
    PELTONEN, L
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (1-2): : 174 - 180
  • [43] Cost-effectiveness analysis of carrier and prenatal genetic testing for X-linked hemophilia
    Tsai, Meng-Che
    Cheng, Chao-Neng
    Wang, Ru-Jay
    Chen, Kow-Tong
    Kuo, Mei-Chin
    Lin, Shio-Jean
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2015, 114 (08) : 722 - 728
  • [44] Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
    Shetty, S.
    Ghosh, K.
    HAEMOPHILIA, 2007, 13 (02) : 172 - 177
  • [45] Maternal caregiving ameliorates the consequences of prenatal maternal psychological distress on child development
    Grande, Leah A.
    Swales, Danielle A.
    Sandman, Curt A.
    Glynn, Laura M.
    Davis, Elysia Poggi
    DEVELOPMENT AND PSYCHOPATHOLOGY, 2022, 34 (04) : 1376 - 1385
  • [46] Mosaicism in carrier of Duchenne muscular dystrophy mutation - Implication for prenatal diagnosis
    Linh Thuy Dinh
    Duc Hinh Nguyen
    Luong, Long Hoang
    Phuong Thi Le
    Tuan Pham Le-Anh
    Dat Quoc Tran
    Thinh Huy Tran
    The-Hung Bui
    Thanh Van Ta
    Van Khanh Tran
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2018, 57 (06): : 878 - 880
  • [47] Prenatal diagnosis of imprinted associated chromosome abnormalities identified by noninvasive prenatal testing (NIPT)
    Haishan Peng
    Dongmei Wang
    Fangfang Guo
    Yaping Hou
    Tingting Hu
    Qianyi Du
    Jiexia Yang
    Scientific Reports, 15 (1)
  • [48] Huntington disease: presymptomatic testing, prenatal diagnosis, preimplantation genetic diagnosis experience
    Durr, A.
    Viville, S.
    GYNECOLOGIE OBSTETRIQUE & FERTILITE, 2007, 35 (10): : 1051 - 1054
  • [49] Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors
    Devers, Patricia L.
    Cronister, Amy
    Ormond, Kelly E.
    Facio, Flavia
    Brasington, Campbell K.
    Flodman, Pamela
    JOURNAL OF GENETIC COUNSELING, 2013, 22 (03) : 291 - 295
  • [50] Prenatal diagnosis and carrier detection for Athabascan severe combined immunodeficiency disease
    Li, LY
    Zhou, YG
    Wang, JH
    Hu, D
    Cowan, MJ
    PRENATAL DIAGNOSIS, 2002, 22 (09) : 763 - 768