Literature DB >> 10875832

Computer support for interpreting family histories of breast and ovarian cancer in primary care: comparative study with simulated cases.

J Emery1, R Walton, M Murphy, J Austoker, P Yudkin, C Chapman, A Coulson, D Glasspool, J Fox.   

Abstract

OBJECTIVES: To evaluate the potential effect of computer support on general practitioners' management of familial breast and ovarian cancer, and to compare the effectiveness of two different types of computer program.
DESIGN: Crossover experiment with balanced block design. PARTICIPANTS: Of a random sample of 100 general practitioners from Buckinghamshire who were invited, 41 agreed to participate. From these, 36 were selected for a fully balanced study.
INTERVENTIONS: Doctors managed 18 simulated cases: 6 with computerised decision support system Risk Assessment in Genetics (RAGs), 6 with Cyrillic (an established pedigree drawing program designed for clinical geneticists), and 6 with pen and paper. MAIN OUTCOME MEASURES: Number of appropriate management decisions made (maximum 6), mean time taken to reach a decision, number of pedigrees accurately drawn (maximum 6). Secondary measures were method of support preferred for particular aspects of managing family histories of cancer; importance of specific information on cancer genetics that might be provided by an "ideal computer program."
RESULTS: RAGs resulted in significantly more appropriate management decisions (median 6) than either Cyrillic (median 3) or pen and paper (median 3); median difference between RAGs and Cyrillic 2.5 (95% confidence interval 2.0 to 3.0; P<0.0001). RAGs also resulted in significantly more accurate pedigrees (median 5) than both Cyrillic (median 3.5) and pen and paper (median 2); median difference between RAGs and Cyrillic 1.5 (1.0 to 2.0; P<0.0001). The time taken to use RAGs (median 178 seconds) was 51 seconds longer per case (95% confidence interval 36 to 65; P<0.0001) than pen and paper (median 124 seconds) but was less than Cyrillic (median 203 seconds; difference 23. (5 to 43; P=0.02)). 33 doctors (92% (78% to 98%)) preferred using RAGs overall. The most important elements of an "ideal computer program" for genetic advice in primary care were referral advice, the capacity to create pedigrees, and provision of evidence and explanations to support advice.
CONCLUSIONS: RAGs could enable general practitioners to be more effective gatekeepers to genetics services, empowering them to reassure the majority of patients with a family history of breast and ovarian cancer who are not at increased genetic risk.

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Mesh:

Year:  2000        PMID: 10875832      PMCID: PMC27423          DOI: 10.1136/bmj.321.7252.28

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


  18 in total

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Authors:  J Emery; E Watson; P Rose; A Andermann
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2.  Computer support for genetic advice in primary care.

Authors:  J Emery
Journal:  Br J Gen Pract       Date:  1999-07       Impact factor: 5.386

Review 3.  Why don't physicians follow clinical practice guidelines? A framework for improvement.

Authors:  M D Cabana; C S Rand; N R Powe; A W Wu; M H Wilson; P A Abboud; H R Rubin
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6.  Effects of computer-based clinical decision support systems on physician performance and patient outcomes: a systematic review.

Authors:  D L Hunt; R B Haynes; S E Hanna; K Smith
Journal:  JAMA       Date:  1998-10-21       Impact factor: 56.272

7.  Preparing health professionals for the genetic revolution.

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8.  Computer support for recording and interpreting family histories of breast and ovarian cancer in primary care (RAGs): qualitative evaluation with simulated patients.

Authors:  J Emery; R Walton; A Coulson; D Glasspool; S Ziebland; J Fox
Journal:  BMJ       Date:  1999-07-03

9.  General practitioners' use of computers during the consultation.

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  29 in total

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Authors:  R A Pagon; L Pinsky; C C Beahler
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Authors:  M H Shere
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4.  Genetic cancer risk assessment in general practice: systematic review of tools available, clinician attitudes, and patient outcomes.

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Review 6.  Reconsidering the family history in primary care.

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Journal:  J Gen Intern Med       Date:  2004-03       Impact factor: 5.128

Review 7.  Clinical decision support for genetically guided personalized medicine: a systematic review.

Authors:  Brandon M Welch; Kensaku Kawamoto
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Review 8.  Lay understanding of familial risk of common chronic diseases: a systematic review and synthesis of qualitative research.

Authors:  Fiona M Walter; Jon Emery; Dejana Braithwaite; Theresa M Marteau
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9.  A primary care audit of familial risk in patients with a personal history of breast cancer.

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Journal:  Fam Cancer       Date:  2014-12       Impact factor: 2.375

10.  A family genetic risk communication framework: guiding tool development in genetics health services.

Authors:  Miriam E Wiens; Brenda J Wilson; Christina Honeywell; Holly Etchegary
Journal:  J Community Genet       Date:  2013-01-15
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