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Published in: Journal of Inherited Metabolic Disease 1/2016

Open Access 01-01-2016 | Original Article

Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups

Authors: Sara D. Khangura, Kylie Tingley, Pranesh Chakraborty, Doug Coyle, Jonathan B. Kronick, Anne-Marie Laberge, Julian Little, Fiona A Miller, John J. Mitchell, Chitra Prasad, Shabnaz Siddiq, Komudi Siriwardena, Rebecca Sparkes, Kathy N. Speechley, Sylvia Stockler, Yannis Trakadis, Brenda J. Wilson, Kumanan Wilson, Beth K. Potter, on behalf of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)

Published in: Journal of Inherited Metabolic Disease | Issue 1/2016

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Abstract

Background

Patient-centered health care for children with inborn errors of metabolism (IEM) and their families is important and requires an understanding of patient experiences, needs, and priorities. IEM-specific patient groups have emerged as important voices within these rare disease communities and are uniquely positioned to contribute to this understanding. We conducted qualitative interviews with IEM patient group representatives to increase understanding of patient and family experiences, needs, and priorities and inform patient-centered research and care.

Methods

We developed a sampling frame of patient groups representing IEM disease communities from Canada, the United States, and United Kingdom. With consent, we interviewed participants to explore their views on experiences, needs, and outcomes that are most important to children with IEM and their families. We analyzed the data using a qualitative descriptive approach to identify key themes and sub-themes.

Results

We interviewed 18 organizational representatives between February 28 and September 17, 2014, representing 16 IEMs and/or disease categories. Twelve participants voluntarily self-identified as parents and/or were themselves patients. Three key themes emerged from the coded data: managing the uncertainty associated with raising and caring for a child with a rare disease; challenges associated with the affected child’s life transitions, and; the collective struggle for improved outcomes and interventions that rare disease communities navigate.

Conclusion

Health care providers can support children with IEM and their families by acknowledging and reducing uncertainty, supporting families through children’s life transitions, and contributing to rare disease communities’ progress toward improved interventions, experiences, and outcomes.
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Metadata
Title
Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups
Authors
Sara D. Khangura
Kylie Tingley
Pranesh Chakraborty
Doug Coyle
Jonathan B. Kronick
Anne-Marie Laberge
Julian Little
Fiona A Miller
John J. Mitchell
Chitra Prasad
Shabnaz Siddiq
Komudi Siriwardena
Rebecca Sparkes
Kathy N. Speechley
Sylvia Stockler
Yannis Trakadis
Brenda J. Wilson
Kumanan Wilson
Beth K. Potter
on behalf of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)
Publication date
01-01-2016
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 1/2016
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-015-9881-1

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