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The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography

BACKGROUND: Adolescent idiopathic scoliosis (AIS) is a common spinal deformity with physical and psychosocial implications for adolescents. The aim of this qualitative evidence synthesis (QES) was to systematically search for, identify, and synthesise qualitative research in order to improve our und...

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Autores principales: Hannink, Erin, Toye, Francine, Newman, Meredith, Barker, Karen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362777/
https://www.ncbi.nlm.nih.gov/pubmed/37481537
http://dx.doi.org/10.1186/s12887-023-04183-y
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author Hannink, Erin
Toye, Francine
Newman, Meredith
Barker, Karen L.
author_facet Hannink, Erin
Toye, Francine
Newman, Meredith
Barker, Karen L.
author_sort Hannink, Erin
collection PubMed
description BACKGROUND: Adolescent idiopathic scoliosis (AIS) is a common spinal deformity with physical and psychosocial implications for adolescents. The aim of this qualitative evidence synthesis (QES) was to systematically search for, identify, and synthesise qualitative research in order to improve our understanding of what it is like to live with AIS and to facilitate empathetic and effective healthcare. METHODS: We systematically searched 4 databases (Medline, EMBASE, PsycINFO and CINAHL) and used the 7 phases of meta-ethnography to synthesise qualitative evidence including studies with children and adolescents, and additional viewpoints from parents about the experience of AIS. RESULTS: We distilled 7 themes. (1) Diagnosis turned time on its head revolves around the AIS diagnosis and the uncertainty of the future that accompanied it. (2) Usual activities no longer the same explores how activities and participation in everyday life are impacted by AIS. (3) Hiding my body describes the pervasive struggle with self-image and appearance. (4) I want to feel normal again explores adolescents’ desire to return to ‘normality’ and challenges of feeling different. (5) Balancing isolation and support considers the relationships in the adolescents’ lives alongside their feelings of isolation. (6) Trying to keep control of treatment decisions explores how adolescents and their parents strive to feel in control. (7) Fearing surgery yet feeling hopeful focused on the apprehension and fear around spinal surgery and the beacon of hope it represented. CONCLUSIONS: Our QES contributes to the understanding of the adolescent experience of living with AIS. From our findings, clinicians can better understand the physical and psychosocial obstacles and the challenges faced throughout the journey of AIS to inform their clinical interactions with these patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-023-04183-y.
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spelling pubmed-103627772023-07-23 The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography Hannink, Erin Toye, Francine Newman, Meredith Barker, Karen L. BMC Pediatr Research BACKGROUND: Adolescent idiopathic scoliosis (AIS) is a common spinal deformity with physical and psychosocial implications for adolescents. The aim of this qualitative evidence synthesis (QES) was to systematically search for, identify, and synthesise qualitative research in order to improve our understanding of what it is like to live with AIS and to facilitate empathetic and effective healthcare. METHODS: We systematically searched 4 databases (Medline, EMBASE, PsycINFO and CINAHL) and used the 7 phases of meta-ethnography to synthesise qualitative evidence including studies with children and adolescents, and additional viewpoints from parents about the experience of AIS. RESULTS: We distilled 7 themes. (1) Diagnosis turned time on its head revolves around the AIS diagnosis and the uncertainty of the future that accompanied it. (2) Usual activities no longer the same explores how activities and participation in everyday life are impacted by AIS. (3) Hiding my body describes the pervasive struggle with self-image and appearance. (4) I want to feel normal again explores adolescents’ desire to return to ‘normality’ and challenges of feeling different. (5) Balancing isolation and support considers the relationships in the adolescents’ lives alongside their feelings of isolation. (6) Trying to keep control of treatment decisions explores how adolescents and their parents strive to feel in control. (7) Fearing surgery yet feeling hopeful focused on the apprehension and fear around spinal surgery and the beacon of hope it represented. CONCLUSIONS: Our QES contributes to the understanding of the adolescent experience of living with AIS. From our findings, clinicians can better understand the physical and psychosocial obstacles and the challenges faced throughout the journey of AIS to inform their clinical interactions with these patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-023-04183-y. BioMed Central 2023-07-22 /pmc/articles/PMC10362777/ /pubmed/37481537 http://dx.doi.org/10.1186/s12887-023-04183-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hannink, Erin
Toye, Francine
Newman, Meredith
Barker, Karen L.
The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
title The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
title_full The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
title_fullStr The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
title_full_unstemmed The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
title_short The experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
title_sort experience of living with adolescent idiopathic scoliosis: a qualitative evidence synthesis using meta-ethnography
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362777/
https://www.ncbi.nlm.nih.gov/pubmed/37481537
http://dx.doi.org/10.1186/s12887-023-04183-y
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