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Advances in Preventive Medicine
Volume 2013 (2013), Article ID 695763, 8 pages
The Use of Family History in Primary Health Care: A Qualitative Study
Department of Family Medicine, Vrije Universiteit Brussel (VUB), Laarbeeklaan 103, 1090 Brussels, Belgium
Received 10 April 2013; Revised 2 July 2013; Accepted 2 July 2013
Academic Editor: Katrin S. Kohl
Copyright © 2013 Sarah Daelemans et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- E. C. Rich, W. Burke, C. J. Heaton et al., “Reconsidering the family history in primary care,” Journal of General Internal Medicine, vol. 19, pp. 273–280, 2004.
- J. P. Evans, C. Skrzynia, and W. Burke, “The complexities of predictive genetic testing,” British Medical Journal, vol. 322, no. 7293, pp. 1052–1056, 2001.
- P. Rose, E. Humm, K. Hey, L. Jones, and S. M. Huson, “Family history taking and genetic counselling in primary care,” Family Practice, vol. 16, no. 1, pp. 78–83, 1999.
- G. Reid and J. Emery, “Chronic disease prevention in general practice—applying the family history,” Australian Family Physician, vol. 35, no. 11, pp. 879–885, 2006.
- P. W. Yoon, M. T. Scheuner, K. L. Peterson-Oehlke, M. Gwinn, A. Faucett, and M. J. Khoury, “Can family history be used as a tool for public health and preventive medicine?” Genetics in Medicine, vol. 4, no. 4, pp. 304–310, 2002.
- R. A. King, J. I. Rotter, and A. G. Motulsky, Eds., The Genetic Basis of Common Diseases, Oxford University Press, New York, NY, USA, 1992.
- P. W. Yoon, M. T. Scheuner, and M. J. Khoury, “Research priorities for evaluating family history in the prevention of common chronic diseases,” American Journal of Preventive Medicine, vol. 24, no. 2, pp. 128–135, 2003.
- N. Qureshi, J. C. Carroll, B. Wilson et al., “The current state of cancer family history collection tools in primary care: a systematic review,” Genetics in Medicine, vol. 11, no. 7, pp. 495–506, 2009.
- B. J. Wilson, J. C. Carroll, J. Allanson et al., “Family history tools in primary care: does one size fit all?” Public Health Genomics, vol. 15, no. 3-4, pp. 181–188, 2012.
- M. T. Scheuner, S. J. Wang, L. J. Raffel, S. K. Larabel, and J. I. Totter, “Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood,” American Journal of Medical Genetics, vol. 71, pp. 315–324, 1997.
- M. T. Scheuner and O. K. Gordon, “Genetic risk assessment for comon diseases,” in Emery and Riomin’s Principal and Practice of Medical Genetics, pp. 654–674, Churchill Livingstone, London, UK, 4th edition, 2002.
- R. Robins and S. Metcalfe, “Integrating genetics as practices of primary care,” Social Science and Medicine, vol. 59, no. 2, pp. 223–233, 2004.
- J. Mathers, S. Greenfield, A. Metcalfe, T. Cole, S. Flanagan, and S. Wilson, “Family history in primary care: understanding GPs' resistance to clinical genetics—qualitative study,” British Journal of General Practice, vol. 60, no. 574, pp. e221–e230, 2010.
- C. Julian-Reynier, I. Nippert, J. Calefato et al., “Genetics in clinical practice: general practitioners' educational priorities in European countries,” Genetics in Medicine, vol. 10, no. 2, pp. 107–113, 2008.
- H. Skirton, C. Lewis, A. Kent, and D. A. Coviello, “Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe,” European Journal of Human Genetics, vol. 18, no. 9, pp. 972–977, 2010.
- M. E. Wood, A. Stockdale, and B. S. Flynn, “Interviews with primary care physicians regarding taking and interpreting the cancer family history,” Family Practice, vol. 25, no. 5, pp. 334–340, 2008.
- E. J. Houwink, S. J. Van Luijk, L. Henneman, C. Van Der Vleuten, G. Jan Dinant, and M. C. Cornel, “Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives,” BMC Family Practice, vol. 12, article 5, 2011.
- R. Gramling, J. Nash, K. Siren, C. Eaton, and L. Culpepper, “Family physician self-efficacy with screening for inherited cancer risk,” Annals of Family Medicine, vol. 2, no. 2, pp. 130–132, 2004.
- M. Fuller, M. Myers, T. Webb, M. Tabangin, and C. Prows, “Primary care providers' responses to patient-generated family history,” Journal of Genetic Counseling, vol. 19, no. 1, pp. 84–96, 2010.
- H. J. Murff, D. Byrne, and S. Syngal, “Cancer risk assessment: quality and impact of the family history interview,” American Journal of Preventive Medicine, vol. 27, no. 3, pp. 239–245, 2004.
- R. L. Bennett, The Practical Guide to the Genetic Family history, Wiley-Liss, New York, NY, USA, 1999.
- J. L. Williams, D. S. Collingridge, and M. S. Williams, “Primary care physicians' experience with family history: an exploratory qualitative study,” Genetics in Medicine, vol. 13, no. 1, pp. 21–25, 2011.
- S. Suther and P. Goodson, “Barriers to the provision of genetic services by primary care physicians: a systematic review of the literature,” Genetics in Medicine, vol. 5, pp. 63–65, 2003.
- Domus Medica, De Gezondheidsgids, http://www.domusmedica.be/documentatie/gezondheidsgids.html.
- J. Ritchie and J. Lewis, Qualitative Research Practice: A Guide for Social Science Students and Researchers, Sage, London, UK, 2003.
- R. T. Acton, N. M. Burst, L. Casebeer et al., “Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics,” Academic Medicine, vol. 75, no. 8, pp. 850–852, 2000.
- S. J. Hayflick, M. P. Eiff, L. Carpenter, and J. Steinberger, “Primary care physicians' utilization and perceptions of genetics services,” Genetics in Medicine, vol. 1, no. 1, pp. 13–21, 1998.
- S. Kumar and M. Gantley, “Tensions between policy makers and general practitioners in implementing new genetics: grounded theory interview study,” British Medical Journal, vol. 319, no. 7222, pp. 1410–1413, 1999.
- M. D. Fetters, D. J. Doukas, and K. L. D. Phan, “Family physicians' perspectives on genetics and the human genome project,” Clinical Genetics, vol. 56, no. 1, pp. 28–34, 1999.
- A. Thoroddsen, G. Sigurjónsdóttir, M. Ehnfors, and A. Ehrenberg, “Accuracy, completeness and comprehensiveness of information on pressure ulcers recorded in the patient record,” Scandinavian Journal of Caring Science, vol. 27, pp. 84–91, 2013.
- A. Ehrenberg, M. Ehnfors, and B. Smedby, “Auditing nursing content in patient records,” Scandinavian Journal of Caring Sciences, vol. 15, no. 2, pp. 133–141, 2001.