Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (75)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Emery, J.
Right arrow Articles by Andermann, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Emery, J.
Right arrow Articles by Andermann, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Family Practice Vol. 16, No. 4, 426-445
© Oxford University Press 1999

A systematic review of the literature exploring the role of primary care in genetic services

Jon Emery, Eila Watsona, Peter Rose and Anne Andermanna

ICRF General Practice Research Group and
a CRC Primary Care Education Research Group, Division of Public Health and Primary Care, Institute of Health Sciences, Old Road, Headington, Oxford OX3 7LF, UK.

Background. In response to growing demands on genetics departments and advances in genetic medicine, it has been proposed that primary care should provide a frontline service in clinical genetics. However, there are concerns that primary care may be unwilling or ill prepared to take on this new role.

Objectives. This study aimed to review systematically the literature exploring the role of primary care in delivering genetic services, and define potential methods of supporting primary care in the provision of genetics services.

Methods. Seven electronic databases were searched. This was complemented by contacting experts in the field and handsearching reference lists. In total, 230 papers were identified, including traditional reviews, of which 96 were examined in detail. Fifty-one papers are included in this review. On account of the heterogeneity of papers identified, we conducted a qualitative synthesis of the results, focusing on five key questions.

Results. GPs accept that they have an increasing role to play in genetics, but lack confidence in their ability to do so because of limited knowledge of clinical genetics. Evidence from pilot studies of cystic fibrosis screening provides the strongest evidence for the feasibility of providing genetic services in primary care.

Conclusions. Although genetic issues currently constitute a relatively small part of the overall workload in primary care, this will almost certainly change in the light of new genetic discoveries. Educational programmes and referral guidelines, computer decision support and genetic nurse specialist outreach clinics may provide useful methods of supporting GPs in the new field of primary care genetics.

Keywords. Family practice, genetic screening, medical genetics, primary health care, review literature..


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Fam PractHome page
M. E Wood, A. Stockdale, and B. S Flynn
Interviews with primary care physicians regarding taking and interpreting the cancer family history
Fam. Pract., September 1, 2008; (2008) cmn053v1.
[Abstract] [Full Text] [PDF]


Home page
BMJHome page
N. C Campbell, E. Murray, J. Darbyshire, J. Emery, A. Farmer, F. Griffiths, B. Guthrie, H. Lester, P. Wilson, and A. L. Kinmonth
Designing and evaluating complex interventions to improve health care
BMJ, March 3, 2007; 334(7591): 455 - 459.
[Full Text] [PDF]


Home page
JCOHome page
L. S. Acheson, S. J. Zyzanski, K. C. Stange, A. Deptowicz, and G. L. Wiesner
Validation of a Self-Administered, Computerized Tool for Collecting and Displaying the Family History of Cancer
J. Clin. Oncol., December 1, 2006; 24(34): 5395 - 5402.
[Abstract] [Full Text] [PDF]


Home page
Fam PractHome page
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]


Home page
JAMAHome page
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]


Home page
J. Clin. Endocrinol. Metab.Home page
A. R. Shuldiner, N. Hoppman, and T. I. Pollin
Hepatic Lipase Genotype, Diabetes Risk, and Implications for Preventative Medicine
J. Clin. Endocrinol. Metab., May 1, 2004; 89(5): 2015 - 2018.
[Full Text] [PDF]


Home page
Ann Fam MedHome page
R. Gramling, J. Nash, K. Siren, C. Eaton, and L. Culpepper
Family Physician Self-Efficacy With Screening for Inherited Cancer Risk
Ann. Fam. Med, March 1, 2004; 2(2): 130 - 132.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
K. D. McKelvey Jr. and J. P. Evans
Cancer Genetics in Primary Care
J. Nutr., November 1, 2003; 133(11): 3767S - 3772.
[Abstract] [Full Text] [PDF]


Home page
Fam PractHome page
J. Knottnerus
Community genetics and community medicine
Fam. Pract., October 1, 2003; 20(5): 601 - 606.
[Abstract] [Full Text] [PDF]


Home page
Fam PractHome page
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]


Home page
Eur Heart JHome page
I.M van Langen, E Birnie, N.J Leschot, G.J Bonsel, and A.A.M Wilde
Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?
Eur. Heart J., March 2, 2003; 24(6): 560 - 566.
[Abstract] [Full Text] [PDF]


Home page
Fam PractHome page
D. Shickle, R. Hapgood, and N. Qureshi
The genetics liaison nurse role as a means of educating and supporting primary care professionals
Fam. Pract., April 1, 2002; 19(2): 193 - 196.
[Abstract] [Full Text] [PDF]


Home page
Fam PractHome page
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]


Home page
Fam PractHome page
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]


Home page
Fam PractHome page
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]


Home page
BMJHome page
J. Emery and S. Hayflick
The challenge of integrating genetic medicine into primary care
BMJ, April 28, 2001; 322(7293): 1027 - 1030.
[Full Text]


Home page
BMJHome page
Women's Concerns Study Group
Raising concerns about family history of breast cancer in primary care consultations: prospective, population based study
BMJ, January 6, 2001; 322(7277): 27 - 28.
[Full Text] [PDF]


Home page
BMJHome page
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]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.