RAGs: A novel approach to computerized genetic risk assessment and decision support from pedigrees

被引:30
作者
Coulson, AS
Glasspool, DW
Fox, J
Emery, J
机构
[1] Imperial Canc Res Fund, Adv Computat Lab, London WC2A 3PX, England
[2] Univ Cambridge, Inst Publ Hlth, Dept Publ Hlth & Primary Care, Gen Pract & Primary Care Res Unit, Cambridge, England
关键词
genetic predisposition; family tree; computer-assisted decision making; primary care;
D O I
10.1055/s-0038-1634427
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Objectives. To assist general practitioners in evaluating patients' genetic risk of cancer on the basis of family history data. Methods: A new computer application, RAGs (Risk Assessment in Genetics), has been developed to help doctors create graphical family trees and assess the genetic risk of breast and colorectal cancer. RAGs possesses two features that distinguish it from similar software: (i) a user-centred design, which takes into account the requirements of the doctor-patient encounter, (ii) effective and accessible risk reporting by employing qualitative evidence for or against increased risk, which is more easily understood than numerical probabilities. The system allows any rule-based genetic risk guideline to be implemented, and may be readily modified to cater for the varying degrees of information required by different specialists. Results: RAGs permits fast, accurate data entry, and results in more appropriate management decisions than those made via other techniques. In addition, RAGs enables both the clinician and the patient to understand how it arrives at its conclusions, since the use of qualitative evidence allows the program to provide explanations for its reasoning. Conclusions: The RAGs system promises to help practitioners be more effective gatekeepers to genetic services. It may empower doctors both to make an informed choice when deciding to refer patients who are at increased genetic risk of breast or colorectal cancer, and to reassure those who are at low risk.
引用
收藏
页码:315 / 322
页数:8
相关论文
共 38 条
[1]   The new genetics - The new genetics in clinical practice [J].
Bell, J .
BMJ-BRITISH MEDICAL JOURNAL, 1998, 316 (7131) :618-620
[2]  
CHAPMAN C, 1999, CYRILLIC PEDIGREE DR
[3]  
Claus EB, 1996, CANCER, V77, P2318, DOI 10.1002/(SICI)1097-0142(19960601)77:11<2318::AID-CNCR21>3.0.CO
[4]  
2-Z
[5]   BRCA1 - Lots of mutations, lots of dilemmas [J].
Collins, FS .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (03) :186-188
[6]  
Cooper R, 1997, PROCEEDINGS OF THE NINETEENTH ANNUAL CONFERENCE OF THE COGNITIVE SCIENCE SOCIETY, P125
[7]  
COULSON A, 2000, RAGS SOFTWARE PEDIGR
[8]   EVIDENCE FOR THE EFFECTIVENESS OF CME - A REVIEW OF 50 RANDOMIZED CONTROLLED TRIALS [J].
DAVIS, DA ;
THOMSON, MA ;
OXMAN, AD ;
HAYNES, RB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (09) :1111-1117
[9]   Can computerised derision support systems deliver improved duality in primary care? [J].
Delaney, BC ;
Fitzmaurice, DA ;
Riaz, A ;
Hobbs, FDR .
BMJ-BRITISH MEDICAL JOURNAL, 1999, 319 (7220) :1281-U11
[10]   A systematic review of the literature exploring the role of primary care in genetic services [J].
Emery, J ;
Watson, E ;
Rose, P ;
Andermann, A .
FAMILY PRACTICE, 1999, 16 (04) :426-445