Literature DB >> 15718186

What does it mean to live with a congenital heart disease? A qualitative study on the lived experiences of adult patients.

Patricia Claessens1, Philip Moons, Bernadette Dierckx de Casterlé, Nancy Cannaerts, Werner Budts, Marc Gewillig.   

Abstract

BACKGROUND: Adults with congenital heart disease constitute a relatively new and continuously growing patient population. In addition to medical problems, patients perceive specific psychosocial concerns that influence their lived experiences and quality of life. AIM: This study aimed to explore the lived experiences of adult congenital heart disease patients.
METHODS: Unstructured, in-depth interviews were performed with 12 patients, aged between 25 and 40 years and suffering from moderate or severe heart defect (tetralogy of Fallot, transposition of the great arteries). Interviews were tape recorded and transcribed verbatim. Data were analyzed using Grounded Theory procedures.
RESULTS: Feeling different was the central theme of the patients' lived experience, as they are faced with physical limitations and visible signs due to the heart defect. The experienced discordance between their world and healthy individuals' world implies that patients struggle constantly with themselves and with their environment to be accepted as normal. The feeling of being different was influenced by attitudes of the environment, health care, and patient's personality. Moreover, it determined the perceived impact of the disease on the patient's daily life.
CONCLUSION: This study shows that normalisation is the most important process when dealing with patients suffering from a congenital heart disease.

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Year:  2005        PMID: 15718186     DOI: 10.1016/j.ejcnurse.2004.12.003

Source DB:  PubMed          Journal:  Eur J Cardiovasc Nurs        ISSN: 1474-5151            Impact factor:   3.908


  17 in total

1.  Quality of life experienced by adolescents and young adults with congenital heart disease.

Authors:  Flávio Miguel Teixeira; Rosália Maria Coelho; Cidália Proença; Ana Margarida Silva; Daniela Vieira; Cláudia Vaz; Cláudia Moura; Victor Viana; José Carlos Areias; Maria Emília Guimarães Areias
Journal:  Pediatr Cardiol       Date:  2011-06-28       Impact factor: 1.655

2.  Parental overprotection and heart-focused anxiety in adults with congenital heart disease.

Authors:  Lephuong Ong; Robert P Nolan; Jane Irvine; Adrienne H Kovacs
Journal:  Int J Behav Med       Date:  2011-09

3.  Psychosocial functioning of adults with congenital heart disease: outcomes of a 30-43 year longitudinal follow-up.

Authors:  Petra Opić; Jolien W Roos-Hesselink; Judith A A Cuypers; Maarten Witsenburg; Annemien van den Bosch; Ron T van Domburg; Ad J J C Bogers; Elisabeth M W J Utens
Journal:  Clin Res Cardiol       Date:  2014-12-07       Impact factor: 5.460

4.  Elements of psychocardiology in the psychosocial handling of adults with congenital heart disease.

Authors:  Edward Callus; Emilia Quadri; Massimo Chessa
Journal:  Front Psychol       Date:  2010-08-11

5.  Coming from behind to win--a qualitative research about psychological conditions of adolescents who have undergone open-heart surgery for single ventricle between the ages 0-5.

Authors:  Oguzhan Zahmacioglu; Cenk Eray Yildiz; Bulent Koca; Murat Ugurlucan; Selman Gokalp; Gurkan Cetin; Ayse Guler Eroglu; Funda Oztunc
Journal:  J Cardiothorac Surg       Date:  2011-11-23       Impact factor: 1.637

6.  Engineering flesh: towards an ethics of lived integrity.

Authors:  Mechteld-Hanna Gertrud Derksen; Klasien Horstman
Journal:  Med Health Care Philos       Date:  2008-02-05

7.  Loss to specialist follow-up in congenital heart disease; out of sight, out of mind.

Authors:  Jo Wray; Alessandra Frigiola; Catherine Bull
Journal:  Heart       Date:  2012-12-20       Impact factor: 5.994

Review 8.  Psychosocial adjustment and quality of life of adolescents and adults with congenital heart disease.

Authors:  Gi Beom Kim
Journal:  Korean J Pediatr       Date:  2014-06-30

9.  Perceived health after percutaneous pulmonary valve implantation: in-depth interviews of patients and next-of-kin.

Authors:  Brith Andresen; Marit Helen Andersen; Harald Lindberg; Gaute Døhlen; Erik Fosse
Journal:  BMJ Open       Date:  2014-07-29       Impact factor: 2.692

10.  Optimism despite profound uncertainty: school and social relationships in adolescents with single ventricle heart disease.

Authors:  Jennifer K Peterson; Ellen F Olshansky; Yuqing Guo; Lorraine S Evangelista; Nancy A Pike
Journal:  Cardiol Young       Date:  2020-11-12       Impact factor: 1.093

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