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Published in: Breast Cancer Research and Treatment 1/2020

Open Access 01-08-2020 | Breast Cancer | Review

A systematic review of communication interventions to help healthcare professionals discuss genetic testing for breast cancer

Authors: Rachel Starkings, Valerie Shilling, Valerie Jenkins, Lesley Fallowfield

Published in: Breast Cancer Research and Treatment | Issue 1/2020

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Abstract

Purpose

This systematic review examined educational training interventions for healthcare professionals (HCPs) discussing genetic testing and risk for hereditary breast cancer. There was a particular focus on the presence, and content, of communication elements within these packages.

Methods

Searches were run via CINAHL, EMBASE, PUBMED, and PsychInfo in February 2019 to identify training interventions available to HCPs with reference to communication skills. Studies were assessed for quality, with relevant intervention and outcome data extracted and synthesized. This review followed the Preferred Reporting Items for Systematic Review and Meta-analyses (PRISMA) statement and was registered on the PROSPERO database (CRD42019124010).

Results

Of 3,988 items, seven papers, two of which were linked, were eligible for inclusion. There was a mix of randomized and single arm studies with web-based and face-to-face interventions. Content included an overview of genetics, hereditary and familial background, and recommended practice techniques. Outcomes focused on communication, self-efficacy, knowledge, and satisfaction. Interventions were designed for genetic counselors, physicians, primary care physicians (PCPs), medical students, and nurses. None of the papers featured oncologists or surgeons.

Conclusions

This review revealed an overall lack of publications which evaluated interventions to assist HCPs discussing hereditary breast cancer risk and testing. Studies failed to operationalize which ‘communication skills’ they included, nor did they consistently report randomization, outcome measures, or analysis.
Discussing the need for, and management of, genetic testing for inherited cancer risk with individuals and their families can be challenging. As genetic testing in breast cancer becomes more common, the provision of specific communication-based training programs, with reference to genetic testing, risk assessments, and counseling skills is warranted.
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Literature
5.
go back to reference Jbilou J, Halilem N, Blouin-Bougie J, Amara N, Landry R, Simard J (2014) Medical genetic counseling for breast cancer in primary care: a synthesis of major determinants of physicians' practices in primary care settings. Public Health Genomics 17(4):190–208. https://doi.org/10.1159/000362358 CrossRefPubMed Jbilou J, Halilem N, Blouin-Bougie J, Amara N, Landry R, Simard J (2014) Medical genetic counseling for breast cancer in primary care: a synthesis of major determinants of physicians' practices in primary care settings. Public Health Genomics 17(4):190–208. https://​doi.​org/​10.​1159/​000362358 CrossRefPubMed
6.
go back to reference Beitsch PD, Whitworth PW, Hughes K, Patel R, Rosen B, Compagnoni G, Baron P, Simmons R, Smith LA, Grady I, Kinney M, Coomer C, Barbosa K, Holmes DR, Brown E, Gold L, Clark P, Riley L, Lyons S, Ruiz A, Kahn S, MacDonald H, Curcio L, Hardwick MK, Yang S, Esplin ED, Nussbaum RL (2019) Underdiagnosis of hereditary breast cancer: are genetic testing guidelines a tool or an obstacle? J Clin Oncol 37(6):453–460. https://doi.org/10.1200/jco.18.01631 CrossRefPubMed Beitsch PD, Whitworth PW, Hughes K, Patel R, Rosen B, Compagnoni G, Baron P, Simmons R, Smith LA, Grady I, Kinney M, Coomer C, Barbosa K, Holmes DR, Brown E, Gold L, Clark P, Riley L, Lyons S, Ruiz A, Kahn S, MacDonald H, Curcio L, Hardwick MK, Yang S, Esplin ED, Nussbaum RL (2019) Underdiagnosis of hereditary breast cancer: are genetic testing guidelines a tool or an obstacle? J Clin Oncol 37(6):453–460. https://​doi.​org/​10.​1200/​jco.​18.​01631 CrossRefPubMed
17.
go back to reference Trepanier A, Ahrens M, McKinnon W, Peters J, Stopfer J, Grumet SC, Manley S, Culver JO, Acton R, Larsen-Haidle J, Correia LA, Bennett R, Pettersen B, Ferlita TD, Costalas JW, Hunt K, Donlon S, Skrzynia C, Farrell C, Callif-Daley F, Vockley CW (2004) Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. J Genet Couns 13(2):83–114. https://doi.org/10.1023/b:jogc.0000018821.48330.77 CrossRefPubMed Trepanier A, Ahrens M, McKinnon W, Peters J, Stopfer J, Grumet SC, Manley S, Culver JO, Acton R, Larsen-Haidle J, Correia LA, Bennett R, Pettersen B, Ferlita TD, Costalas JW, Hunt K, Donlon S, Skrzynia C, Farrell C, Callif-Daley F, Vockley CW (2004) Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. J Genet Couns 13(2):83–114. https://​doi.​org/​10.​1023/​b:​jogc.​0000018821.​48330.​77 CrossRefPubMed
21.
go back to reference Riley BD, Culver JO, Skrzynia C, Senter LA, Peters JA, Costalas JW, Callif-Daley F, Grumet SC, Hunt KS, Nagy RS, McKinnon WC, Petrucelli NM, Bennett RL, Trepanier AM (2012) Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors. J Genet Couns 21(2):151–161. https://doi.org/10.1007/s10897-011-9462-x CrossRefPubMed Riley BD, Culver JO, Skrzynia C, Senter LA, Peters JA, Costalas JW, Callif-Daley F, Grumet SC, Hunt KS, Nagy RS, McKinnon WC, Petrucelli NM, Bennett RL, Trepanier AM (2012) Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors. J Genet Couns 21(2):151–161. https://​doi.​org/​10.​1007/​s10897-011-9462-x CrossRefPubMed
41.
go back to reference Houwink EJ, Muijtjens AM, van Teeffelen SR, Henneman L, Rethans JJ, van der Jagt LE, van Luijk SJ, Dinant GJ, van der Vleuten C, Cornel MC (2014) Effectiveness of oncogenetics training on general practitioners' consultation skills: a randomized controlled trial. Genet Med 16(1):45–52. https://doi.org/10.1038/gim.2013.69 CrossRefPubMed Houwink EJ, Muijtjens AM, van Teeffelen SR, Henneman L, Rethans JJ, van der Jagt LE, van Luijk SJ, Dinant GJ, van der Vleuten C, Cornel MC (2014) Effectiveness of oncogenetics training on general practitioners' consultation skills: a randomized controlled trial. Genet Med 16(1):45–52. https://​doi.​org/​10.​1038/​gim.​2013.​69 CrossRefPubMed
43.
go back to reference Lee J, Cho HJ, Yoo H-W, Park SK, Yang JJ, Kim S-W, Kang E, Ahn S-H, Lee S-J, Suh YJ, Kim SY, Kim E-K, Moon NM, Lee MH, Korean Hereditary Breast Cancer Research Group KBCS (2013) The effects of a genetic counseling educational program on hereditary breast cancer for korean healthcare providers. J Breast Cancer 16(3):335–341. https://doi.org/10.4048/jbc.2013.16.3.335 CrossRef Lee J, Cho HJ, Yoo H-W, Park SK, Yang JJ, Kim S-W, Kang E, Ahn S-H, Lee S-J, Suh YJ, Kim SY, Kim E-K, Moon NM, Lee MH, Korean Hereditary Breast Cancer Research Group KBCS (2013) The effects of a genetic counseling educational program on hereditary breast cancer for korean healthcare providers. J Breast Cancer 16(3):335–341. https://​doi.​org/​10.​4048/​jbc.​2013.​16.​3.​335 CrossRef
Metadata
Title
A systematic review of communication interventions to help healthcare professionals discuss genetic testing for breast cancer
Authors
Rachel Starkings
Valerie Shilling
Valerie Jenkins
Lesley Fallowfield
Publication date
01-08-2020
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 1/2020
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-020-05741-z

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