Literature DB >> 14682357

Attitudes of health care trainees about genetics and disability: issues of access, health care communication, and decision making.

Kelly E Ormond1, Carol J Gill, Patrick Semik, Kristi L Kirschner.   

Abstract

Prior studies suggest that knowledge and attitudes of health care professionals influence patient communication and medical decision-making. To study this dynamic in the context of genetic disability, we developed a survey on health professionals' attitudes regarding disability and genetic screening and pilot-tested it on a sample of medical students, residents, and genetic counseling students (N=85). Despite minimal experience with disability or genetics, most respondents reported feeling comfortable dealing with genetics (59%) and disability (75%). The majority felt that disability caused significant suffering for both the person (51%) and family (64%), and that research should be directed toward preventing genetic disability (62%). Similar to prior literature, perceived "Quality of Life" was most often based on degrees of physical and cognitive functioning, pain, and social support. However, differences were found between genetic counseling trainees and other medical trainees in their relative emphasis of social versus medical issues in questions of disability and genetic testing, and these response patterns were associated with differences in the groups' priorities for offering information about social resources. Respondents agreed that access to genetic testing and information is personal and that testing should be available upon request for oneself (68%) and to a lesser degree for one's fetus (55%) or child (41%). However, the same individuals frequently stated that society should regulate access to such technologies. Although most felt that the patient and professional should jointly make such decisions on a case-by-case basis, it was also seen as appropriate for the health care professional to occasionally decline genetic testing. It seems appropriate that training and experience influence knowledge and attitudes. Therefore, it is critical to document knowledge and attitudes of various health care providers and trainees, including differences between various specialties, to improve educational interventions geared to this area.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2003        PMID: 14682357     DOI: 10.1023/a:1023953022290

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  36 in total

1.  Assessing genetic risk: comparison between the referring obstetrician and genetic counselor.

Authors:  K L Koscica; J C Canterino; J T Harrigan; T Dalaya; C V Ananth; A M Vintzileos
Journal:  Am J Obstet Gynecol       Date:  2001-11       Impact factor: 8.661

Review 2.  The intersection of genetics, public health, and preventive medicine.

Authors:  S S Coughlin
Journal:  Am J Prev Med       Date:  1999-02       Impact factor: 5.043

3.  Empirical evidence that genetic counseling is directive: where do we go from here?

Authors:  B A Bernhardt
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

4.  The disability paradox: high quality of life against all odds.

Authors:  G L Albrecht; P J Devlieger
Journal:  Soc Sci Med       Date:  1999-04       Impact factor: 4.634

5.  The genetic testing of children.

Authors:  T M Marteau
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

6.  The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

Authors:  A Clarke
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

7.  Neonatal end-of-life decision making: Physicians' attitudes and relationship with self-reported practices in 10 European countries.

Authors:  M Rebagliato; M Cuttini; L Broggin; I Berbik; U de Vonderweid; G Hansen; M Kaminski; L A Kollée; A Kucinskas; S Lenoir; A Levin; J Persson; M Reid; R Saracci
Journal:  JAMA       Date:  2000-11-15       Impact factor: 56.272

8.  Spinal cord injury: a search for determinants of depression two years after the event.

Authors:  A R Craig; K M Hancock; H G Dickson
Journal:  Br J Clin Psychol       Date:  1994-05

9.  Ventilator use by muscular dystrophy association patients.

Authors:  J R Bach
Journal:  Arch Phys Med Rehabil       Date:  1992-02       Impact factor: 3.966

10.  Physician characteristics associated with decisions to withdraw life support.

Authors:  N A Christakis; D A Asch
Journal:  Am J Public Health       Date:  1995-03       Impact factor: 9.308

View more
  8 in total

1.  Medical education and disability studies.

Authors:  Fiona Kumari Campbell
Journal:  J Med Humanit       Date:  2009-12

2.  Challenges for providing genetic counselling in Colombian genetic clinics: the viewpoint of the physicians providing genetic consultations.

Authors:  Clemencia Rodas-Pérez; Angus Clarke; John Powell; Margaret Thorogood
Journal:  J Community Genet       Date:  2015-06-19

Review 3.  The relationship between the genetic counseling profession and the disability community: a commentary.

Authors:  Anne C Madeo; Barbara B Biesecker; Campbell Brasington; Lori H Erby; Kathryn F Peters
Journal:  Am J Med Genet A       Date:  2011-05-12       Impact factor: 2.802

4.  Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study.

Authors:  C Roadhouse; C Shuman; K Anstey; K Sappleton; D Chitayat; E Ignagni
Journal:  J Genet Couns       Date:  2018-06-16       Impact factor: 2.537

5.  Are patient rights to information and self-determination in diagnostic genetic testing upheld? A comparison of patients' and providers' perceptions.

Authors:  Tarja Nyrhinen; Marja Hietala; Pauli Puukka; Helena Leino-Kilpi
Journal:  J Genet Couns       Date:  2008-11-01       Impact factor: 2.537

6.  Reprogenetics, reproductive risks and cultural awareness: what may we learn from Israeli and Croatian medical students?

Authors:  Miriam Ethel Bentwich; Michal Mashiach-Eizenberg; Ana Borovečki; Frida Simonstein
Journal:  BMC Med Ethics       Date:  2019-11-27       Impact factor: 2.652

7.  Examining the relationship between genetic counselors' attitudes toward deaf people and the genetic counseling session.

Authors:  Emily E Enns; Patrick Boudreault; Christina G S Palmer
Journal:  J Genet Couns       Date:  2009-11-11       Impact factor: 2.537

8.  Exploring general practitioners' experience of informing women about prenatal screening tests for foetal abnormalities: a qualitative focus group study.

Authors:  Cate Nagle; Sharon Lewis; Bettina Meiser; Jane Gunn; Jane Halliday; Robin Bell
Journal:  BMC Health Serv Res       Date:  2008-05-28       Impact factor: 2.655

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.