Literature DB >> 8211278

The use of preventive health care services: carrier testing for the genetic disorder haemophilia.

I Varekamp1, T P Suurmeijer, F R Rosendaal, A H Bröcker-Vriends.   

Abstract

A retrospective study was performed to explore carrier testing among women who were possible or obligate carriers of the haemophilia gene. Knowledge of the possibility of carrier testing and use of carrier testing were studied separately. In our exploration we were guided by the diffusion theory and the Health Belief Model. Logistic regression analysis showed that four factors were statistically significant related to knowledge of carrier testing: information via mass media, a haemophilic relative in the nuclear family rather than in the extended family, medical severity of haemophilia, and information from the patients' organization. For those women acquainted with carrier testing two of the four factors just mentioned were significantly related to the utilization of carrier testing i.e. having a haemophilic relative in the nuclear family and the medical severity of the haemophilia. In addition the following factors were associated: attitude towards abortion because of haemophilia, educational level, and marital status. Notwithstanding the prominent function of the mass media and the patients' organization, the respondents themselves stated that relatives, especially parents and sisters, were the most important source of information on genetic counselling and carrier testing.

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Year:  1993        PMID: 8211278     DOI: 10.1016/0277-9536(93)90103-b

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  4 in total

1.  Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.

Authors:  Pascal Borry; Gerry Evers-Kiebooms; Martina C Cornel; Angus Clarke; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

2.  Genetic counseling for pregnant adolescents.

Authors:  T Peters-Brown; L Fry-Mehltretter
Journal:  J Genet Couns       Date:  1996-12       Impact factor: 2.537

3.  Uptake of Genetic Counseling, Knowledge of Bleeding risks and Psychosocial Impact in a South African Cohort of Female Relatives of People with Hemophilia.

Authors:  Anne Gillham; Brenda Greyling; Tina-Marie Wessels; Bongi Mbele; Rosemarie Schwyzer; Amanda Krause; Johnny Mahlangu
Journal:  J Genet Couns       Date:  2015-04-02       Impact factor: 2.537

4.  Preventing lives affected by hemophilia: A mixed methods study of the views of adults with hemophilia and their families toward genetic screening.

Authors:  Felicity K Boardman; Rachel Hale; Raksha Gohel; Philip J Young
Journal:  Mol Genet Genomic Med       Date:  2019-03-05       Impact factor: 2.183

  4 in total

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