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Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours

BACKGROUND: This study investigates the severeness of participation barriers in patients surviving paediatric posterior fossa tumours (PFT) many years after treatment. In the past, aetiological studies on adverse outcome have primarily focused on pathobiological risk factors. The current analysis ai...

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Autores principales: Hoffmann‐Lamplmair, Doris, Gram, Alexandra, Krottendorfer, Kerstin, Peyrl, Andreas, Leiss, Ulrike, Czech, Thomas, Slavc, Irene, Pletschko, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083959/
https://www.ncbi.nlm.nih.gov/pubmed/35708465
http://dx.doi.org/10.1111/cch.13023
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author Hoffmann‐Lamplmair, Doris
Gram, Alexandra
Krottendorfer, Kerstin
Peyrl, Andreas
Leiss, Ulrike
Czech, Thomas
Slavc, Irene
Pletschko, Thomas
author_facet Hoffmann‐Lamplmair, Doris
Gram, Alexandra
Krottendorfer, Kerstin
Peyrl, Andreas
Leiss, Ulrike
Czech, Thomas
Slavc, Irene
Pletschko, Thomas
author_sort Hoffmann‐Lamplmair, Doris
collection PubMed
description BACKGROUND: This study investigates the severeness of participation barriers in patients surviving paediatric posterior fossa tumours (PFT) many years after treatment. In the past, aetiological studies on adverse outcome have primarily focused on pathobiological risk factors. The current analysis aims to investigate the importance of environmental variables. METHODS: On average, 10 years after diagnosis, educational and social difficulties of 42 patients surviving paediatric PFT (mean age 17 years) were inquired using a self‐constructed questionnaire following the Psychosocial Resource‐Orientated Assessment (PREDI). Educational or social participation barriers were defined by self‐ and/or proxy‐reported difficulties in school or in peer relationships. Accordingly, the children and adolescents were categorized into groups of adequate and limited participation. Subsequently, the study identified potential pathobiological (treatment type, hydrocephalus, tumour relapse, gender, age at diagnosis, seizures and cerebellar mutism) and environmental (parental and maternal education, siblings, main language, discrepancies between personal and environmental values, regular physical activity and private living space) risk factors and investigated whether patients with adequate and limited participation differed in the number of risk factors. RESULTS: Almost one decade after treatment, two thirds of patients experienced educational and/or social difficulties. Patients with limited participation were more frequently associated with environmental factors such as low maternal education degree, siblings, main language other than German, discrepancies between societal and personal values and irregular physical activity, as well as the pathobiological risk factors treatment type, hydrocephalus, tumour relapse, cerebellar mutism and seizures. These variables significantly discriminated between patients with and without limited participation. CONCLUSIONS: Limited participation in patients treated for paediatric PFT is common. Next to pathobiological, also environmental risk factors play a major role in educational and social participation barriers. This highlights the fact that solely considering pathobiology is not sufficient when investigating risk factors for the emergence of late sequelae. Future aetiological studies must adopt a biopsychosocial perspective.
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spelling pubmed-100839592023-04-11 Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours Hoffmann‐Lamplmair, Doris Gram, Alexandra Krottendorfer, Kerstin Peyrl, Andreas Leiss, Ulrike Czech, Thomas Slavc, Irene Pletschko, Thomas Child Care Health Dev Research Articles BACKGROUND: This study investigates the severeness of participation barriers in patients surviving paediatric posterior fossa tumours (PFT) many years after treatment. In the past, aetiological studies on adverse outcome have primarily focused on pathobiological risk factors. The current analysis aims to investigate the importance of environmental variables. METHODS: On average, 10 years after diagnosis, educational and social difficulties of 42 patients surviving paediatric PFT (mean age 17 years) were inquired using a self‐constructed questionnaire following the Psychosocial Resource‐Orientated Assessment (PREDI). Educational or social participation barriers were defined by self‐ and/or proxy‐reported difficulties in school or in peer relationships. Accordingly, the children and adolescents were categorized into groups of adequate and limited participation. Subsequently, the study identified potential pathobiological (treatment type, hydrocephalus, tumour relapse, gender, age at diagnosis, seizures and cerebellar mutism) and environmental (parental and maternal education, siblings, main language, discrepancies between personal and environmental values, regular physical activity and private living space) risk factors and investigated whether patients with adequate and limited participation differed in the number of risk factors. RESULTS: Almost one decade after treatment, two thirds of patients experienced educational and/or social difficulties. Patients with limited participation were more frequently associated with environmental factors such as low maternal education degree, siblings, main language other than German, discrepancies between societal and personal values and irregular physical activity, as well as the pathobiological risk factors treatment type, hydrocephalus, tumour relapse, cerebellar mutism and seizures. These variables significantly discriminated between patients with and without limited participation. CONCLUSIONS: Limited participation in patients treated for paediatric PFT is common. Next to pathobiological, also environmental risk factors play a major role in educational and social participation barriers. This highlights the fact that solely considering pathobiology is not sufficient when investigating risk factors for the emergence of late sequelae. Future aetiological studies must adopt a biopsychosocial perspective. John Wiley and Sons Inc. 2022-06-22 2023-01 /pmc/articles/PMC10083959/ /pubmed/35708465 http://dx.doi.org/10.1111/cch.13023 Text en © 2022 The Authors. Child: Care, Health and Development published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Hoffmann‐Lamplmair, Doris
Gram, Alexandra
Krottendorfer, Kerstin
Peyrl, Andreas
Leiss, Ulrike
Czech, Thomas
Slavc, Irene
Pletschko, Thomas
Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
title Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
title_full Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
title_fullStr Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
title_full_unstemmed Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
title_short Sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
title_sort sociocultural variables have a major impact on participation in patients treated for paediatric posterior fossa tumours
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083959/
https://www.ncbi.nlm.nih.gov/pubmed/35708465
http://dx.doi.org/10.1111/cch.13023
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