Literature DB >> 15604637

Patients' knowledge of cystic fibrosis: genetic determinism and implications for treatment.

Elizabeth Chapman1, Diana Bilton.   

Abstract

This paper uses the self-regulation model of illness perceptions (Leventhal et al. , 1984) to consider the implications of different ways of thinking about the causes of illness. The relationship between anxiety/depression and knowledge or denial of illness is also considered. These issues are explored using adherence to treatment in cystic fibrosis (CF) as an example. Twenty-six CF patients took part in semistructured interviews and completed a standardized anxiety and depression scale (HAD, Zigmond and Snaith, 1983). Interview data were analyzed using Interpretative Phenomenological Analysis (Chapman and Smith, 2002). HAD data were analyzed using SPSS. The respondents displayed widely differing levels of knowledge of their condition. Some deterministic comments were also reported. Findings are discussed in relation to the information that physicians might provide to patients and families in the light of increasing knowledge about genetics in society and the genotyping of individuals with genetic conditions specifically. Any important gaps in patient knowledge could usefully be discussed at transition from pediatric to adult care and issues relating to control and genetic determinism discussed with the patients individually.

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Year:  2004        PMID: 15604637     DOI: 10.1023/B:JOGC.0000044199.38694.6c

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


  31 in total

1.  Alcohol and drug use in second-year medical students at the University of Leeds.

Authors:  M Pickard; L Bates; M Dorian; H Greig; D Saint
Journal:  Med Educ       Date:  2000-02       Impact factor: 6.251

2.  The social and ethical implications of changing medical technologies: the views of people living with genetic conditions.

Authors:  Elizabeth Chapman
Journal:  J Health Psychol       Date:  2002-03

Review 3.  Causal attributions in physical illness.

Authors:  T Sensky
Journal:  J Psychosom Res       Date:  1997-12       Impact factor: 3.006

Review 4.  Non-adherence with medications in organ transplant patients: a literature review.

Authors:  S P Wainwright; D Gould
Journal:  J Adv Nurs       Date:  1997-11       Impact factor: 3.187

5.  Association between genetically determined pancreatic status and lung disease in adult cystic fibrosis patients.

Authors:  Yann Loubières; Dominique Grenet; Brigitte Simon-Bouy; Jacques Medioni; Paul Landais; Claude Férec; Marc Stern
Journal:  Chest       Date:  2002-01       Impact factor: 9.410

6.  Will genetic testing for predisposition for disease result in fatalism? A qualitative study of parents responses to neonatal screening for familial hypercholesterolaemia.

Authors:  V Senior; T M Marteau; T J Peters
Journal:  Soc Sci Med       Date:  1999-06       Impact factor: 4.634

7.  Health perceptions and treatment adherence in adults with cystic fibrosis.

Authors:  J Abbott; M Dodd; A K Webb
Journal:  Thorax       Date:  1996-12       Impact factor: 9.139

Review 8.  Psychological consequences of predictive genetic testing: a systematic review.

Authors:  M Broadstock; S Michie; T Marteau
Journal:  Eur J Hum Genet       Date:  2000-10       Impact factor: 4.246

9.  Different perceptions of disease severity and self care between patients with cystic fibrosis, their close companions, and physician.

Authors:  J Abbott; M Dodd; A K Webb
Journal:  Thorax       Date:  1995-07       Impact factor: 9.139

Review 10.  The management of young adults with cystic fibrosis: 'genes, jeans and genies'.

Authors:  S Elborn
Journal:  Disabil Rehabil       Date:  1998 Jun-Jul       Impact factor: 3.033

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  7 in total

Review 1.  Illness representations, self-regulation, and genetic counseling: a theoretical review.

Authors:  Shoshana Shiloh
Journal:  J Genet Couns       Date:  2006-10       Impact factor: 2.537

2.  Assessment of psychosocial outcomes in genetic counseling research: an overview of available measurement scales.

Authors:  Nadine A Kasparian; Claire E Wakefield; Bettina Meiser
Journal:  J Genet Couns       Date:  2007-08-13       Impact factor: 2.537

3.  Living with multiple endocrine neoplasia type 1: decent care-insufficient medical and genetic information: a qualitative study of MEN 1 patients in a Swedish hospital.

Authors:  Nina Strømsvik; Karin Nordin; Gunilla Berglund; Lars F Engebretsen; Mats G Hansson; Eva Gjengedal
Journal:  J Genet Couns       Date:  2007-02-03       Impact factor: 2.537

4.  Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.

Authors:  Mary-Anne Young; Laura Elenor Forrest; Victoria-Mae Rasmussen; Paul James; Gillian Mitchell; Sarah Dilys Sawyer; Katrina Reeve; Nina Hallowell
Journal:  J Genet Couns       Date:  2017-11-22       Impact factor: 2.537

5.  Are patient rights to information and self-determination in diagnostic genetic testing upheld? A comparison of patients' and providers' perceptions.

Authors:  Tarja Nyrhinen; Marja Hietala; Pauli Puukka; Helena Leino-Kilpi
Journal:  J Genet Couns       Date:  2008-11-01       Impact factor: 2.537

6.  The stigmatising implications of presenting schizophrenia as a genetic disease.

Authors:  Laura Bennett; Kathryn Thirlaway; Alexandra J Murray
Journal:  J Genet Couns       Date:  2008-09-05       Impact factor: 2.537

Review 7.  Achieving adolescent adherence to treatment of major depression.

Authors:  Dennis Staton
Journal:  Adolesc Health Med Ther       Date:  2010-08-04
  7 in total

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