Literature DB >> 19177338

Family communication, genetic testing and colonoscopy screening in hereditary non-polyposis colon cancer: a qualitative study.

Siobhan McCann1, Domhnall MacAuley, Yvonne Barnett, Brendan Bunting, Aoife Bradley, Lisa Jeffers, Patrick J Morrison.   

Abstract

OBJECTIVE: Genetic testing and colonoscopy is recommended for people with a strong history of colorectal cancer (CRC). However, families must communicate so that all members are aware of the risk. The study aimed to explore the factors influencing family communication about genetic risk and colonoscopy among people with a strong family history of CRC who attended a genetic clinic with a view to having a genetic test for hereditary non-polyposis colon cancer (HNPCC).
METHODS: Interviews were held with 30 people with a high familial risk of colon cancer. The transcripts were transcribed verbatim and analysed using Interpretative Phenomenological Analysis.
RESULTS: The family context, family history and perceptions about family duties and responsibilities were important motivators for communication about risk, genetic testing and colonoscopy and influenced participation in genetic testing and screening programmes. Participants reported usually communicating openly with their relatives about genetic risk and colonoscopy. Individuals felt a duty towards affected relatives and to their own children. The influence of the spouse and other relatives, particularly those affected by CRC, was also important. Colonoscopy was perceived to be embarrassing, unpleasant and sometimes painful. While there was sometimes anxiety about the result of the colonoscopy the results were usually reassuring.
CONCLUSIONS: The family context and the experience of the family history can have an impact on communication, genetic testing and screening in HNPCC and this should be explored during counselling. Some individuals might benefit from support in communicating with relatives about genetic risk. Ways of improving the individual's experience of colonoscopy should also be examined.

Entities:  

Mesh:

Year:  2009        PMID: 19177338     DOI: 10.1002/pon.1487

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  29 in total

1.  Understanding patterns of health communication in families at risk for hereditary nonpolyposis colorectal cancer: examining the effect of conclusive versus indeterminate genetic test results.

Authors:  Anne L Ersig; Donald W Hadley; Laura M Koehly
Journal:  Health Commun       Date:  2011-06-24

Review 2.  Specific psychosocial issues of individuals undergoing genetic counseling for cancer - a literature review.

Authors:  Willem Eijzenga; Daniela E E Hahn; Neil K Aaronson; Irma Kluijt; Eveline M A Bleiker
Journal:  J Genet Couns       Date:  2013-08-31       Impact factor: 2.537

3.  Balancing life with an increased risk of cancer: lived experiences in healthy individuals with Lynch syndrome.

Authors:  Helle Vendel Petersen; Mef Nilbert; Inge Bernstein; Christina Carlsson
Journal:  J Genet Couns       Date:  2014-01-08       Impact factor: 2.537

4.  Worldwide Practice Patterns in Lynch Syndrome Diagnosis and Management, Based on Data From the International Mismatch Repair Consortium.

Authors:  Jennifer Y Pan; Robert W Haile; Allyson Templeton; Finlay Macrae; FeiFei Qin; Vandana Sundaram; Uri Ladabaum
Journal:  Clin Gastroenterol Hepatol       Date:  2018-04-24       Impact factor: 11.382

5.  Family Communication in Inherited Cardiovascular Conditions in Ireland.

Authors:  Sinead Whyte; Andrew Green; Marion McAllister; Hannah Shipman
Journal:  J Genet Couns       Date:  2016-06-08       Impact factor: 2.537

6.  A Typology of Communication Dynamics in Families Living a Slow-Motion Technological Disaster.

Authors:  Heather Orom; Rebecca J W Cline; Tanis Hernandez; Lisa Berry-Bobovski; Ann G Schwartz; John C Ruckdeschel
Journal:  J Fam Issues       Date:  2012-10

7.  Families' experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population.

Authors:  Álvaro Mendes; Liliana Sousa
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

8.  Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis.

Authors:  Jenna Petersen; Cathryn Koptiuch; Yelena P Wu; Ryan Mooney; Ashley Elrick; Kathryn Szczotka; Megan Keener; Lisa Pappas; Priyanka Kanth; Andrew Soisson; Wendy Kohlmann; Kimberly A Kaphingst
Journal:  Patient Educ Couns       Date:  2018-07-26

9.  What women with breast cancer discuss with clinicians about risk for their adolescent daughters.

Authors:  Erin Maloney; Shawna Edgerson; Mark Robson; Ken Offit; Richard Brown; Carma Bylund; David W Kissane
Journal:  J Psychosoc Oncol       Date:  2012

10.  Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.

Authors:  Kristen Dilzell; Kerry Kingham; Kelly Ormond; Uri Ladabaum
Journal:  Fam Cancer       Date:  2014-09       Impact factor: 2.375

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