Interactive e-counselling for genetics pre-test decisions: where are we now?
- PMID: 24828354
- DOI: 10.1111/cge.12430
Interactive e-counselling for genetics pre-test decisions: where are we now?
Abstract
In-person genetic counselling (GC) is the model typically used to provide patients with information regarding their genetic testing options. Current and emerging demand for genetic testing may overburden the health care system and exceed the available numbers of genetic counsellors. Furthermore, GC is not always available at times and places convenient for patients. There is little evidence that the in-person model alone is always optimal and alternatives to in-person GC have been studied in genetics and other areas of health care. This review summarizes the published evidence between 1994 and March 2014 for interactive e-learning and decisional support e-tools that could be used in pre-test GC. A total of 21 papers from 15 heterogeneous studies of interactive e-learning tools, with or without decision aids, were reviewed. Study populations, designs, and outcomes varied widely but most used an e-tool as an adjunct to conventional GC. Knowledge acquisition and decisional comfort were achieved and the e-tools were generally well-accepted by users. In a time when health care budgets are constrained and availability of GC is limited, research is needed to determine the specific circumstances in which e-tools might replace or supplement some of the functions of genetic counsellors.
Keywords: decision aids; decision-making; e-counselling; e-learning; e-tools genetic counselling; genetic testing.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Similar articles
-
DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.J Genet Couns. 2016 Dec;25(6):1298-1308. doi: 10.1007/s10897-016-9971-8. Epub 2016 May 23. J Genet Couns. 2016. PMID: 27211035
-
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.BMJ Open. 2022 Apr 29;12(4):e060899. doi: 10.1136/bmjopen-2022-060899. BMJ Open. 2022. PMID: 35487723 Free PMC article.
-
Genetic counselling in the era of genomic medicine.Br Med Bull. 2018 Jun 1;126(1):27-36. doi: 10.1093/bmb/ldy008. Br Med Bull. 2018. PMID: 29617718 Free PMC article. Review.
-
American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.J Clin Oncol. 2003 Jun 15;21(12):2397-406. doi: 10.1200/JCO.2003.03.189. Epub 2003 Apr 11. J Clin Oncol. 2003. PMID: 12692171
-
Changing views on the goal of reproductive genetic counselling in Hungary.Eur J Obstet Gynecol Reprod Biol. 2008 Mar;137(1):3-9. doi: 10.1016/j.ejogrb.2007.10.003. Epub 2007 Dec 11. Eur J Obstet Gynecol Reprod Biol. 2008. PMID: 18063291 Review.
Cited by
-
Interventions Facilitating Family Communication of Genetic Testing Results and Cascade Screening in Hereditary Breast/Ovarian Cancer or Lynch Syndrome: A Systematic Review and Meta-Analysis.Cancers (Basel). 2021 Feb 23;13(4):925. doi: 10.3390/cancers13040925. Cancers (Basel). 2021. PMID: 33672149 Free PMC article. Review.
-
Personalized Medicine Implementation with Non-traditional Data Sources: A Conceptual Framework and Survey of the Literature.Yearb Med Inform. 2019 Aug;28(1):181-189. doi: 10.1055/s-0039-1677916. Epub 2019 Aug 16. Yearb Med Inform. 2019. PMID: 31419830 Free PMC article. Review.
-
Development of patient "profiles" to tailor counseling for incidental genomic sequencing results.Eur J Hum Genet. 2019 Jul;27(7):1008-1017. doi: 10.1038/s41431-019-0352-2. Epub 2019 Mar 8. Eur J Hum Genet. 2019. PMID: 30846854 Free PMC article.
-
The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.Eur J Hum Genet. 2018 Jul;26(7):984-995. doi: 10.1038/s41431-018-0144-0. Epub 2018 Apr 27. Eur J Hum Genet. 2018. PMID: 29703952 Free PMC article.
-
Queensland Consumers' Awareness and Understanding of Clinical Genetics Services.Front Genet. 2020 Oct 15;11:537743. doi: 10.3389/fgene.2020.537743. eCollection 2020. Front Genet. 2020. PMID: 33193608 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous