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Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives
BACKGROUND: To explore parents’ experiences and perceptions on informational, management and relational continuity of care for children with special health care needs from hospitalization to the first months after discharge to the home. METHODS: Semi-structured interviews and a focus group were carr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328636/ https://www.ncbi.nlm.nih.gov/pubmed/25882884 http://dx.doi.org/10.1186/s13052-015-0114-x |
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author | Zanello, Elisa Calugi, Simona Rucci, Paola Pieri, Giulia Vandini, Silvia Faldella, Giacomo Fantini, Maria Pia |
author_facet | Zanello, Elisa Calugi, Simona Rucci, Paola Pieri, Giulia Vandini, Silvia Faldella, Giacomo Fantini, Maria Pia |
author_sort | Zanello, Elisa |
collection | PubMed |
description | BACKGROUND: To explore parents’ experiences and perceptions on informational, management and relational continuity of care for children with special health care needs from hospitalization to the first months after discharge to the home. METHODS: Semi-structured interviews and a focus group were carried out to capture parents’ experiences and perceptions. Transcripts were analyzed using a directed approach to the qualitative content analysis. RESULTS: 16 families participated to this study: 13 were involved in interviews (10 face-to-face and 3 by phone) and 3 in a focus group, within 1–6 months after discharge from the University Hospital of Bologna (S.Orsola/Malpighi) and from hospitals of Bologna Province. To parents of children with special health care needs, the three domains of continuity of care were relevant in a whole but with different key elements during hospitalization, at discharge and after discharge. Moreover, empowerment emerged from parents’ narratives as essential to help parents cope with the transition from the hospital setting to the new responsibilities connected with the home care of their child. Parent’s perceptions about the family pediatrician concerned his/her centrality in the activation and coordination of the healthcare network. Moreover, parents exhibited different attitudes towards involvement in decision making: some wished and expected to be involved, others preferred not to be involved. CONCLUSIONS: Care coordination for children with special care needs is a complex process that need to be attended to during the hospitalization phase and after discharge to the community. The findings of this study may contribute to elucidating the perceptions and experiences of parents with children with special health care needs about the continuity of care from hospital to community care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13052-015-0114-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4328636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43286362015-02-15 Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives Zanello, Elisa Calugi, Simona Rucci, Paola Pieri, Giulia Vandini, Silvia Faldella, Giacomo Fantini, Maria Pia Ital J Pediatr Research BACKGROUND: To explore parents’ experiences and perceptions on informational, management and relational continuity of care for children with special health care needs from hospitalization to the first months after discharge to the home. METHODS: Semi-structured interviews and a focus group were carried out to capture parents’ experiences and perceptions. Transcripts were analyzed using a directed approach to the qualitative content analysis. RESULTS: 16 families participated to this study: 13 were involved in interviews (10 face-to-face and 3 by phone) and 3 in a focus group, within 1–6 months after discharge from the University Hospital of Bologna (S.Orsola/Malpighi) and from hospitals of Bologna Province. To parents of children with special health care needs, the three domains of continuity of care were relevant in a whole but with different key elements during hospitalization, at discharge and after discharge. Moreover, empowerment emerged from parents’ narratives as essential to help parents cope with the transition from the hospital setting to the new responsibilities connected with the home care of their child. Parent’s perceptions about the family pediatrician concerned his/her centrality in the activation and coordination of the healthcare network. Moreover, parents exhibited different attitudes towards involvement in decision making: some wished and expected to be involved, others preferred not to be involved. CONCLUSIONS: Care coordination for children with special care needs is a complex process that need to be attended to during the hospitalization phase and after discharge to the community. The findings of this study may contribute to elucidating the perceptions and experiences of parents with children with special health care needs about the continuity of care from hospital to community care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13052-015-0114-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-08 /pmc/articles/PMC4328636/ /pubmed/25882884 http://dx.doi.org/10.1186/s13052-015-0114-x Text en © Zanello et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zanello, Elisa Calugi, Simona Rucci, Paola Pieri, Giulia Vandini, Silvia Faldella, Giacomo Fantini, Maria Pia Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
title | Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
title_full | Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
title_fullStr | Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
title_full_unstemmed | Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
title_short | Continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
title_sort | continuity of care in children with special healthcare needs: a qualitative study of family’s perspectives |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328636/ https://www.ncbi.nlm.nih.gov/pubmed/25882884 http://dx.doi.org/10.1186/s13052-015-0114-x |
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