Family Practice Vol. 16, No. 5, 468-474
© Oxford University Press 1999
GPs' views on their role in cancer genetics services and current practice
Imperial Cancer Medical Oncology Unit, Western General Hospital, Edinburgh EH4 2XU,
a Department of Public Health Sciences, University of Edinburgh, Medical School, Teviot Place, Edinburgh EH8 9AG,
b Clinical Genetics Department, Molecular Medicine Centre, Western General Hospital, Edinburgh EH14 5JG and
c Lothian Health, Deaconess House, 148 Pleasance, Edinburgh EH8 9RS, UK.
Dr A Fry, Department of Clinical Psychology, Outpatient Building, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
Background. Increasing demand for cancer genetics services has necessitated an urgent review of how these services are organized and, in particular, identification of an effective role for primary care.
Objectives. We aimed to assess the views of GPs on their role in cancer genetics services and their confidence in performing that role; to assess their understanding of cancer genetics, current practice and referral behaviour; and to identify needs for information and training to enable GPs to play an effective role in these services.
Method. A cross-sectional questionnaire survey of GPs was conducted through general practices in SE Scotland; 397 (response rate 59.3%) GPs returned a completed questionnaire. Outcome measures were: responders' perceptions of their role in cancer genetics services; confidence within that role; understanding of cancer genetics; current practice regarding patients presenting with concerns about their family history of cancer; and perceived information and training needs.
Results. GPs identified their role to be: taking a family history; making appropriate referrals to specialist services; providing emotional support; teaching breast self-examination; and discussing need for screening. Lack of confidence within this role was reflected in low levels of understanding of cancer genetics and in inappropriate referral practices. Concerns were expressed about the increasingly specialist role demanded of primary care. A desire for referral guidelines and community genetics clinics was identified.
Conclusions. GPs readily identify a role for themselves in cancer genetics services, but admit to a lack of confidence in this area, calling for clear referral guidelines and specialist community support. Current inappropriate referral to specialist services results from a lack of confidence in estimating cancer risk, highlighting the need for the development of clear referral criteria. Given the rapidly increasing demand for cancer genetics services and the vital role of primary care, it is important to identify a model of these services that facilitates effective involvement of GPs without further increasing their workload.
Keywords. Cancer, family practice, genetics, primary health care.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. B. White, V. L. Bonham, J. Jenkins, N. Stevens, and C. M. McBride Too Many Referrals of Low-Risk Women for BRCA1/2 Genetic Services by Family Physicians Cancer Epidemiol. Biomarkers Prev., November 1, 2008; 17(11): 2980 - 2986. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E Wood, A. Stockdale, and B. S Flynn Interviews with primary care physicians regarding taking and interpreting the cancer family history Fam. Pract., October 1, 2008; 25(5): 334 - 340. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. L. Trotter and H. M. Martin Family History in Pediatric Primary Care Pediatrics, September 1, 2007; 120(SUPPLEMENT_2): S60 - S65. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Gilbar Communicating genetic information in the family: the familial relationship as the forgotten factor J. Med. Ethics, July 1, 2007; 33(7): 390 - 393. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. J Wilson, N. Torrance, J. Mollison, M S. Watson, A. Douglas, Z. Miedzybrodzka, R. Gordon, S. Wordsworth, M. Campbell, N. Haites, et al. Cluster randomized trial of a multifaceted primary care decision-support intervention for inherited breast cancer risk Fam. Pract., October 1, 2006; 23(5): 537 - 544. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. M. Walter, J. Emery, D. Braithwaite, and T. M. Marteau Lay Understanding of Familial Risk of Common Chronic Diseases: A Systematic Review and Synthesis of Qualitative Research Ann. Fam. Med, November 1, 2004; 2(6): 583 - 594. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. J. Murff, D. R. Spigel, and S. Syngal Does This Patient Have a Family History of Cancer?: An Evidence-Based Analysis of the Accuracy of Family Cancer History JAMA, September 22, 2004; 292(12): 1480 - 1489. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Green, S. K. Peterson, M. W. Baker, G. R. Harper, L. C. Friedman, W. S. Rubinstein, and D. T. Mauger Effect of a Computer-Based Decision Aid on Knowledge, Perceptions, and Intentions About Genetic Testing for Breast Cancer Susceptibility: A Randomized Controlled Trial JAMA, July 28, 2004; 292(4): 442 - 452. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Knottnerus Community genetics and community medicine Fam. Pract., October 1, 2003; 20(5): 601 - 606. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M Aalfs, E. M. Smets, H. C. de Haes, and N. J Leschot Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs Fam. Pract., April 1, 2003; 20(2): 135 - 141. [Abstract] [Full Text] [PDF] |
||||
![]() |
N Qureshi, R Hapgood, and S Armstrong Continuous medical education approaches for clinical genetics: a postal survey of general practitioners J. Med. Genet., November 1, 2002; 39(11): e69 - 69. [Full Text] [PDF] |
||||
![]() |
M McAllister, K O'Malley, P Hopwood, B Kerr, A Howell, and D G R Evans Management of women with a family history of breast cancer in the North West Region of England: training for implementing a vision of the future J. Med. Genet., July 1, 2002; 39(7): 531 - 535. [Full Text] [PDF] |
||||
![]() |
G. Elwyn, R. Iredale, and J. Gray Reactions of GPs to a triage-controlled referral system for cancer genetics Fam. Pract., February 1, 2002; 19(1): 65 - 71. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. M. Sweet, T. L. Bradley, and J. A. Westman Identification and Referral of Families at High Risk for Cancer Susceptibility J. Clin. Oncol., January 15, 2002; 20(2): 528 - 537. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Bankhead, J. Emery, N. Qureshi, H. Campbell, J. Austoker, and E. Watson New developments in genetics--knowledge, attitudes and information needs of practice nurses Fam. Pract., October 1, 2001; 18(5): 475 - 486. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. W Rose, E. Watson, P. Yudkin, J. Emery, M. Murphy, A. Fuller, and A. Lucassen Referral of patients with a family history of breast/ovarian cancer--GPs' knowledge and expectations Fam. Pract., October 1, 2001; 18(5): 487 - 490. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. M Walter, A. L. Kinmonth, F. Hyland, P. Murrell, T. M Marteau, and C. Todd Experiences and expectations of the new genetics in relation to familial risk of breast cancer: a comparison of the views of GPs and practice nurses Fam. Pract., October 1, 2001; 18(5): 491 - 494. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Watson, J. Austoker, and A. Lucassen A study of GP referrals to a family cancer clinic for breast/ovarian cancer Fam. Pract., April 1, 2001; 18(2): 131 - 134. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Emery, R. Walton, M. Murphy, J. Austoker, P. Yudkin, C. Chapman, A. Coulson, D. Glasspool, and J. Fox Computer support for interpreting family histories of breast and ovarian cancer in primary care: comparative study with simulated cases BMJ, July 1, 2000; 321(7252): 28 - 32. [Abstract] [Full Text] |
||||








