ArticleBMJ (Clinical research ed.)2000
Computer support for interpreting family histories of breast and ovarian cancer in primary care: comparative study with simulated cases.
Article in BMJ (Clinical research ed.), 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 4 of them syntheses that pooled it.
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Who cites it
31 citing papers in PubMed, 4 syntheses or guidelines pooled it.
- Genetic cancer risk assessment in general practice: systematic review of tools available, clinician attitudes, and patient outcomes.The British journal of general practice : the journal of the Royal College of General Practitioners · 2019Pooled it
- Guidelines for genetic risk assessment of hereditary breast and ovarian cancer: early disagreements and low utilization.Journal of general internal medicine · 2009Guideline
- Clinical decision support for genetically guided personalized medicine: a systematic review.Journal of the American Medical Informatics Association : JAMIAPooled it
- Lay understanding of familial risk of common chronic diseases: a systematic review and synthesis of qualitative research.Annals of family medicinePooled it
- Effectiveness of oncogenetics training on general practitioners' consultation skills: a randomized controlled trial.Genetics in medicine : official journal of the American College of Medical Genetics · 2014Trial
- The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary care.British journal of cancer · 2007Trial
- A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes.British journal of cancer · 2004Trial
- A randomized trial of specialist genetic assessment: psychological impact on women at different levels of familial breast cancer risk.British journal of cancer · 2002Trial
- Current and Emerging Strategies for Tubo-Ovarian Cancer Diagnostics.Diagnostics (Basel, Switzerland) · 2023Review
- OpenClinical.net: Artificial intelligence and knowledge engineering at the point of care.BMJ health & care informatics · 2020Review
- Guideline-based Clinical Decision Support Systems as an Inseparable Tool for Better Cancer Care Management.Iranian journal of public health · 2016Article
- Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners.British journal of cancer · 2015Article
- A primary care audit of familial risk in patients with a personal history of breast cancer.Familial cancer · 2014Article
- A family genetic risk communication framework: guiding tool development in genetics health services.Journal of community genetics · 2013Article
- Delivering pharmacogenetic testing in a primary care setting.Pharmacogenomics and personalized medicine · 2013Article
- Patient interest in recording family histories of cancer via the Internet.Genetics in medicine : official journal of the American College of Medical Genetics · 2008Article
- Mentoring nurses in familial cancer risk assessment and counseling: lessons learned from a formative evaluation.Journal of genetic counseling · 2008Article
- Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol.BMC cancer · 2007Article
- Designing and evaluating complex interventions to improve health care.BMJ (Clinical research ed.) · 2007Review
- Evidence-based guidelines and decision support services: A discussion and evaluation in triple assessment of suspected breast cancer.British journal of cancer · 2006Article
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectivesTo 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.
designCrossover experiment with balanced block design.
participantsOf 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.
interventionsDoctors 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 measuresNumber 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."
resultsRAGs 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.
conclusionsRAGs 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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