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. 1997 Oct;34(10):831–837. doi: 10.1136/jmg.34.10.831

Evaluation of a project to enhance knowledge of hereditary diseases and management.

I R Walpole 1, C Watson 1, D Moore 1, J Goldblatt 1, C Bower 1
PMCID: PMC1051090  PMID: 9350816

Abstract

During 1992 and 1993, in a designated suburban area of Perth, Western Australia, information on hereditary disease was provided for health professionals and the general community. This information was in the form of posters, pamphlets, postal flyers and return letter cards, a static display, newspaper articles, advertisements and radio broadcasts, and professional seminars. The aim of this project was to evaluate the effectiveness of combined strategies to convey practical information about hereditary disease to the community and health professionals. Multiple measures of response evaluation were used, which included structured questionnaire surveys of health professionals and members of the community before and after the project. In the community surveys, respondents who were female, married, middle aged, and parents, and had a higher level of education or were born in Australia, New Zealand, or the United Kingdom were generally better informed about hereditary diseases. This intervention resulted in only meagre changes in community knowledge about hereditary disease, even though promotional materials were shown to be appropriate. General Practitioners (GPs) and Child Health Nurses (CHNs) were supportive of clinical genetic services and recognised a need for continuation of education in this field. There is a rapidly increasing need for community and health professional comprehension of the applications of the new genetic technology. This project indicates that routine educational and health promotion strategies will not be enough to achieve desired levels of knowledge and attitude change.

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Selected References

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  1. Borgaonkar D. S. Genetics Week in Delaware: a new concept in genetics education for health-care providers in the community. Am J Hum Genet. 1992 Jul;51(1):220–221. [PMC free article] [PubMed] [Google Scholar]
  2. Clayton E. W., Hannig V. L., Pfotenhauer J. P., Parker R. A., Campbell P. W., 3rd, Phillips J. A., 3rd Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening. Am J Hum Genet. 1996 Mar;58(3):617–627. [PMC free article] [PubMed] [Google Scholar]
  3. Clayton E. W., Hannig V. L., Pfotenhauer J. P., Parker R. A., Campbell P. W., 3rd, Phillips J. A., 3rd Teaching about cystic fibrosis carrier screening by using written and video information. Am J Hum Genet. 1995 Jul;57(1):171–181. [PMC free article] [PubMed] [Google Scholar]
  4. Czeizel A. E., Intôdy Z., Modell B. What proportion of congenital abnormalities can be prevented? BMJ. 1993 Feb 20;306(6876):499–503. doi: 10.1136/bmj.306.6876.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Danks D. M. Whither genetic services? Med J Aust. 1993 Aug 16;159(4):221–222. [PubMed] [Google Scholar]
  6. Faden R. R., Tambor E. S., Chase G. A., Geller G., Hofman K. J., Holtzman N. A. Attitudes of physicians and genetics professionals toward cystic fibrosis carrier screening. Am J Med Genet. 1994 Mar 1;50(1):1–11. doi: 10.1002/ajmg.1320500102. [DOI] [PubMed] [Google Scholar]
  7. Garver K. L., LeChien K. Geneticists' responsibility to other health care professionals and to the lay public. Am J Hum Genet. 1992 Oct;51(4):922–923. [PMC free article] [PubMed] [Google Scholar]
  8. Girgis A., Sanson-Fisher R. Community based health education: general practitioners' perceptions of their role and willingness to participate. Aust N Z J Public Health. 1996 Aug;20(4):381–385. doi: 10.1111/j.1467-842x.1996.tb01050.x. [DOI] [PubMed] [Google Scholar]
  9. Graham J. M., Jr, Rotter J. I., Riccardi V. M., Baird P. A., Benkendorf J., Bodurtha J., Childs B., Davidson R., Huether C. A., Laing K. Report of the Task Force on Teaching Human Genetics in North American Medical Schools. Am J Hum Genet. 1989 Jan;44(1):161–165. [PMC free article] [PubMed] [Google Scholar]
  10. Harper Peter. Genetics and public health. BMJ. 1992 Mar 14;304(6828):721–721. doi: 10.1136/bmj.304.6828.721. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Harris R., Elles R., Craufurd D., Dodge A., Ivinson A., Hodgkinson K., Mountford R., Schwartz M., Strachan T., Read A. Molecular genetics in the National Health Service in Britain. J Med Genet. 1989 Apr;26(4):219–225. doi: 10.1136/jmg.26.4.219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Modell B. Cystic fibrosis screening and community genetics. J Med Genet. 1990 Aug;27(8):475–479. doi: 10.1136/jmg.27.8.475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Myers M. F., Bernhardt B. A., Tambor E. S., Holtzman N. A. Involving consumers in the development of an educational program for cystic fibrosis carrier screening. Am J Hum Genet. 1994 Apr;54(4):719–726. [PMC free article] [PubMed] [Google Scholar]
  14. Naylor E. W. Genetic screening and genetic counseling: knowledge, attitudes, and practices in two groups of family planning professionals. Soc Biol. 1975 Winter;22(4):304–314. doi: 10.1080/19485565.1975.9988187. [DOI] [PubMed] [Google Scholar]
  15. Ponder M., Lee J., Green J., Richards M. Family history and perceived vulnerability to some common diseases: a study of young people and their parents. J Med Genet. 1996 Jun;33(6):485–492. doi: 10.1136/jmg.33.6.485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Richards M., Ponder M. Lay understanding of genetics: a test of a hypothesis. J Med Genet. 1996 Dec;33(12):1032–1036. doi: 10.1136/jmg.33.12.1032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Rowley P. T., Loader S., Levenkron J. C., Phelps C. E. Cystic fibrosis carrier screening: knowledge and attitudes of prenatal care providers. Am J Prev Med. 1993 Sep-Oct;9(5):261–266. [PubMed] [Google Scholar]
  18. Scriver C. R., Bardanis M., Cartier L., Clow C. L., Lancaster G. A., Ostrowsky J. T. Beta-thalassemia disease prevention: genetic medicine applied. Am J Hum Genet. 1984 Sep;36(5):1024–1038. [PMC free article] [PubMed] [Google Scholar]
  19. Weitz R. Barriers to acceptance of genetic counseling among primary care physicians. Soc Biol. 1979 Fall;26(3):189–197. doi: 10.1080/19485565.1979.9988377. [DOI] [PubMed] [Google Scholar]
  20. Welkenhuysen M., Evers-Kiebooms G., Decruyenaere M., Van den Berghe H., Bande-Knops J., Van Gerven V. Adolescents' attitude towards carrier testing for cystic fibrosis and its relative stability over time. Eur J Hum Genet. 1996;4(1):52–62. doi: 10.1159/000472170. [DOI] [PubMed] [Google Scholar]
  21. Wilfond B. S., Nolan K. National policy development for the clinical application of genetic diagnostic technologies. Lessons from cystic fibrosis. JAMA. 1993 Dec 22;270(24):2948–2954. [PubMed] [Google Scholar]

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