Literature DB >> 15789153

Evaluating the impact of genetic counseling and testing with signal detection methods.

Christina G S Palmer1, Donald W Hadley.   

Abstract

One measure of the impact of genetic counseling and testing (GCT) is the extent to which it fosters behavioral change that is consistent with mutation status. We describe and illustrate how two different signal detection methods, receiver operating characteristic (ROC) analysis and recursive partitioning, can be used in this context to evaluate the impact of GCT. We analyzed real screening behavior data obtained in the 12 months following GCT for Hereditary Nonpolyposis Colon Cancer (HNPCC) using these two different signal detection approaches. Each approach demonstrated that GCT had an impact on behavioral outcomes, and was effective in fostering behavioral outcomes appropriate to mutation status. The ROC approach demonstrated that GCT was effective because mutation positive and mutation negative individuals could be distinguished on the basis of the number of recommended screening behaviors. The recursive partitioning approach demonstrated that GCT was effective because there were generally high rates of adherence to screening guidelines among subjects. The recursive partitioning technique also identified four subgroups of subjects, each with distinct characteristics, for which tailored interventions could be developed to increase rates of adherence to screening guidelines. Signal detection methods are easily implemented and are useful techniques for evaluating the impact of GCT.

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Year:  2005        PMID: 15789153     DOI: 10.1007/s10897-005-1497-4

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  27 in total

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Journal:  J Genet Couns       Date:  1995-09       Impact factor: 2.537

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Journal:  Health Psychol       Date:  1997-07       Impact factor: 4.267

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Journal:  CMAJ       Date:  1996-04-15       Impact factor: 8.262

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Journal:  Radiology       Date:  1982-04       Impact factor: 11.105

Review 7.  Genetic counseling and interpretation of genetic tests in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.

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Journal:  Dis Colon Rectum       Date:  2001-02       Impact factor: 4.585

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Journal:  J Natl Cancer Inst       Date:  1997-01-15       Impact factor: 13.506

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Journal:  Am J Public Health       Date:  1995-08       Impact factor: 9.308

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  4 in total

1.  Assessing the predictive accuracy of hMLH1 and hMSH2 mutation probability models.

Authors:  Kory W Jasperson; Katrina Lowstuter; Jeffrey N Weitzel
Journal:  J Genet Couns       Date:  2006-10       Impact factor: 2.537

2.  From ideas to efficacy: The ORBIT model for developing behavioral treatments for chronic diseases.

Authors:  Susan M Czajkowski; Lynda H Powell; Nancy Adler; Sylvie Naar-King; Kim D Reynolds; Christine M Hunter; Barbara Laraia; Deborah H Olster; Frank M Perna; Janey C Peterson; Elissa Epel; Josephine E Boyington; Mary E Charlson
Journal:  Health Psychol       Date:  2015-02-02       Impact factor: 4.267

3.  Use of a patient-entered family health history tool with decision support in primary care: impact of identification of increased risk patients on genetic counseling attendance.

Authors:  Adam H Buchanan; Carol A Christianson; Tiffany Himmel; Karen P Powell; Astrid Agbaje; Geoffrey S Ginsburg; Vincent C Henrich; Lori A Orlando
Journal:  J Genet Couns       Date:  2014-08-15       Impact factor: 2.537

4.  Protocol for the "Implementation, adoption, and utility of family history in diverse care settings" study.

Authors:  R Ryanne Wu; Rachel A Myers; Catherine A McCarty; David Dimmock; Michael Farrell; Deanna Cross; Troy D Chinevere; Geoffrey S Ginsburg; Lori A Orlando
Journal:  Implement Sci       Date:  2015-11-24       Impact factor: 7.327

  4 in total

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