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Narrative analysis of adults with complex congenital heart disease: Childhood experiences and their lifelong reverberations

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1 Toronto Congenital Cardiac Centre for Adults, Peter Munk Cardiac Centre, University of Toronto, Toronto, Ontario, Canada
2 Knight Cardiovascular Institute, Oregon Heath & Science University, Portland, Orgeon, USA
3 The Hospital for Sick Children, Toronto, Ontario, Canada

* Corresponding Author: S. Lucy Roche, Division of Cardiology, 5N-521 Toronto General Hospital, 585 University Avenue, Toronto, M5G 2N2, Ontario, Canada. Email: email

Congenital Heart Disease 2018, 13(5), 740-747. https://doi.org/10.1111/chd.12647

Abstract

Background: With access to surgical care, >90% of today’s infants with congenital heart disease (CHD) will reach adulthood. During childhood, survivors accrue a wealth of health care experience and develop strategies for navigating life with a chronic disease.
Methods: Seeking to learn from this individualized process, we invited adults with complex CHD to participate in narrative analysis—an established qualitative research method for studying how individuals derive meaning from their personal stories. Audio recordings of 2‐4 hour free‐form interviews were transcribed and iteratively analyzed to identify common themes and detect similarities or differences in language, viewpoint and interpretation. Recruitment continued until saturation was reached (n = 10).
Results: While each narrative was unique, CHD had a pervasive effect on the autobiography of all participants. Seven themes were discussed consistently: (1) parental/sibling relationships, (2) physical limitations, (3) embarrassment/denial, (4) memories of pediatric health care, (5) transition to adult care, (6) education and career choices, and (7) relationship and reproductive choices. While some of the recalled experiences were negative, all participants also spoke positively about the effect of CHD on their lives.
Conclusions: Adults with CHD provide the voices of expert witnesses; illuminating how the pediatric journey influences their identity, choices, personal relationships and adult health care interactions. These narratives could inform and improve the contemporary care of children with heart disease.

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APA Style
Keir, M., Bailey, B., Lee, A., Kovacs, A.H., Roche, S.L. (2018). Narrative analysis of adults with complex congenital heart disease: childhood experiences and their lifelong reverberations. Congenital Heart Disease, 13(5), 740-747. https://doi.org/10.1111/chd.12647
Vancouver Style
Keir M, Bailey B, Lee A, Kovacs AH, Roche SL. Narrative analysis of adults with complex congenital heart disease: childhood experiences and their lifelong reverberations. Congeni Heart Dis. 2018;13(5):740-747 https://doi.org/10.1111/chd.12647
IEEE Style
M. Keir, B. Bailey, A. Lee, A.H. Kovacs, and S.L. Roche, “Narrative analysis of adults with complex congenital heart disease: Childhood experiences and their lifelong reverberations,” Congeni. Heart Dis., vol. 13, no. 5, pp. 740-747, 2018. https://doi.org/10.1111/chd.12647



cc Copyright © 2018 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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