Literature DB >> 35304074

A systematic review of theory-informed strategies used in interventions fostering family genetic risk communication.

Jingsong Zhao1, Yue Guan2, Colleen M McBride2.   

Abstract

BACKGROUND: Inherited risk is a family issue. Identifying family members who carry a pathogenic genetic variant that increases risk of cancers and other chronic diseases can be lifesaving for those affected.
OBJECTIVE: The research questions are: (1) which family communication frameworks have been applied, (2) how do intervention strategies employed map to these theories, and (3) to what extent were families receptive to these strategies and communication increased?
METHODS: Manuscripts published between January 2010 and August 2020 were searched in three databases: PubMed, PsycINFO, and Web of Science.
RESULTS: Nine intervention trials were identified. All interventions were evaluated in clinical genetic counseling contexts using at least one individual-level strategy (e.g. increase knowledge). Only three focused on dyadic conversations such as preparing for relatives' information needs.
CONCLUSIONS: This systematic review posed the question whether theoretically based approaches have been applied to foster family genetic risk communication. Greater attention needs to be paid to the utilization of dyadic level and family system level theories to guide intervention developments. PRACTICAL IMPLICATIONS: We conclude by calling for accelerating and broadening the development of interventions to enable family communication about inherited risk that are theory-based, incorporate family-systems thinking, and are conducted outside of specialty clinic settings.
Copyright © 2022. Published by Elsevier B.V.

Entities:  

Keywords:  Cancer prevention; Family communication; Genetic risk; Hereditary conditions; Theory

Mesh:

Year:  2022        PMID: 35304074      PMCID: PMC9203975          DOI: 10.1016/j.pec.2022.03.009

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  66 in total

1.  Does enhanced information at cancer genetic counseling improve counselees' knowledge, risk perception, satisfaction and negotiation of information to at-risk relatives?--a randomized study.

Authors:  Afsaneh Hayat Roshanai; Richard Rosenquist; Claudia Lampic; Karin Nordin
Journal:  Acta Oncol       Date:  2009       Impact factor: 4.089

2.  Unpacking the blockers: understanding perceptions and social constraints of health communication in hereditary breast ovarian cancer (HBOC) susceptibility families.

Authors:  June A Peters; Regina Kenen; Lindsey M Hoskins; Laura M Koehly; Barry Graubard; Jennifer T Loud; Mark H Greene
Journal:  J Genet Couns       Date:  2011-05-06       Impact factor: 2.537

Review 3.  Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review.

Authors:  Lisa L Shah; Sandra Daack-Hirsch
Journal:  J Genet Couns       Date:  2018-02-28       Impact factor: 2.537

4.  The Adaptome: Advancing the Science of Intervention Adaptation.

Authors:  David A Chambers; Wynne E Norton
Journal:  Am J Prev Med       Date:  2016-06-28       Impact factor: 5.043

Review 5.  Diagnosis and clinical management of long-QT syndrome.

Authors:  Christian Steinberg
Journal:  Curr Opin Cardiol       Date:  2018-01       Impact factor: 2.161

6.  Familial communication and cascade testing among relatives of BRCA population screening participants.

Authors:  Sari Lieberman; Amnon Lahad; Ariela Tomer; Sivan Koka; Malka BenUziyahu; Aviad Raz; Ephrat Levy-Lahad
Journal:  Genet Med       Date:  2018-03-29       Impact factor: 8.822

7.  Design and Feasibility of an Intervention to Support Cancer Genetic Counselees in Informing their At-Risk Relatives.

Authors:  Eveline de Geus; Willem Eijzenga; Fred H Menko; Rolf H Sijmons; Hanneke C J M de Haes; Cora M Aalfs; Ellen M A Smets
Journal:  J Genet Couns       Date:  2016-04-22       Impact factor: 2.537

8.  Interrater reliability: the kappa statistic.

Authors:  Mary L McHugh
Journal:  Biochem Med (Zagreb)       Date:  2012       Impact factor: 2.313

9.  Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.

Authors:  Jan M Hodgson; Sylvia A Metcalfe; Maryanne Aitken; Susan M Donath; Clara L Gaff; Ingrid M Winship; Martin B Delatycki; Loane L C Skene; Belinda J McClaren; Jean L Paul; Jane L Halliday
Journal:  BMC Med Genet       Date:  2014-03-14       Impact factor: 2.103

10.  The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.

Authors:  Erica Sermijn; Liesbeth Delesie; Ellen Deschepper; Ingrid Pauwels; Maryse Bonduelle; Erik Teugels; Jacques De Grève
Journal:  Fam Cancer       Date:  2016-04       Impact factor: 2.375

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  2 in total

1.  Perceptions and care Recommendations from Previvors: Qualitative analysis of female BRCA1/2 mutation Carriers' experience with genetic testing and counseling.

Authors:  Kate E Dibble; Laura K M Donorfio; Preston A Britner; Keith M Bellizzi
Journal:  Gynecol Oncol Rep       Date:  2022-05-02

2.  The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband-Provider and Proband-Family Communication in Hereditary Breast and Ovarian Cancer.

Authors:  Carla Pedrazzani; Monica Aceti; Reka Schweighoffer; Andrea Kaiser-Grolimund; Nicole Bürki; Pierre O Chappuis; Rossella Graffeo; Christian Monnerat; Olivia Pagani; Manuela Rabaglio; Maria C Katapodi; Maria Caiata-Zufferey
Journal:  J Pers Med       Date:  2022-07-29
  2 in total

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