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The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature
BACKGROUND: There are a growing number of children and young people (CYP) with chronic health needs or complex disabilities. Increasingly, CYP with life‐limiting or life‐threatening conditions are surviving into adulthood. Communication between CYP, their family, and health professionals can be chal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519173/ https://www.ncbi.nlm.nih.gov/pubmed/30817012 http://dx.doi.org/10.1111/cch.12652 |
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author | Diffin, Janet Byrne, Bronagh Kerr, Helen Price, Jayne Abbott, Aine McLaughlin, Dorry O'Halloran, Peter |
author_facet | Diffin, Janet Byrne, Bronagh Kerr, Helen Price, Jayne Abbott, Aine McLaughlin, Dorry O'Halloran, Peter |
author_sort | Diffin, Janet |
collection | PubMed |
description | BACKGROUND: There are a growing number of children and young people (CYP) with chronic health needs or complex disabilities. Increasingly, CYP with life‐limiting or life‐threatening conditions are surviving into adulthood. Communication between CYP, their family, and health professionals can be challenging. The use of a personal health record (PHR) is one potential strategy for improving communication by promoting CYP's health advocacy skills. However, PHR implementation has proved difficult due to technical, organisational, and professional barriers. The aim of this realist review is to identify the factors, which help or hinder the use of PHRs with CYP living with a complex health condition. METHODS: Systematic realist review. Literature was sourced from six databases: Medline, Embase, CINAHL, PsychInfo, The Cochrane Library, and Science Direct (from 1946 to August Week 3 2018). The web was searched to identify grey literature. Articles were sourced from reference lists of included studies. Data were extracted using a standardised data extraction form. Two reviewers completed data extraction and synthesis. Methodological rigor was assessed using the relevant Critical Appraisal Skills Programme tool. RESULTS: Nine articles were included. Contextual factors, which helped implementation, included the CYP having a high perception of need for a PHR and a high level of desire for self‐management. Service providers and CYP need knowledge about the purpose and benefits of the PHR, and organisations need a dedicated person to facilitate PHR use. Mechanisms triggered by the PHR included improved understanding and knowledge of health care condition(s) for CYP, an increased feeling of control over condition(s), and more active engagement in their health care. Outcomes for CYP included improved self‐advocacy and communication. CONCLUSION: Clearer definitions of which young people would benefit from using a PHR must be established to inform which organisations and service providers would be best suited to PHR implementation. |
format | Online Article Text |
id | pubmed-6519173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65191732019-05-21 The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature Diffin, Janet Byrne, Bronagh Kerr, Helen Price, Jayne Abbott, Aine McLaughlin, Dorry O'Halloran, Peter Child Care Health Dev Review Articles BACKGROUND: There are a growing number of children and young people (CYP) with chronic health needs or complex disabilities. Increasingly, CYP with life‐limiting or life‐threatening conditions are surviving into adulthood. Communication between CYP, their family, and health professionals can be challenging. The use of a personal health record (PHR) is one potential strategy for improving communication by promoting CYP's health advocacy skills. However, PHR implementation has proved difficult due to technical, organisational, and professional barriers. The aim of this realist review is to identify the factors, which help or hinder the use of PHRs with CYP living with a complex health condition. METHODS: Systematic realist review. Literature was sourced from six databases: Medline, Embase, CINAHL, PsychInfo, The Cochrane Library, and Science Direct (from 1946 to August Week 3 2018). The web was searched to identify grey literature. Articles were sourced from reference lists of included studies. Data were extracted using a standardised data extraction form. Two reviewers completed data extraction and synthesis. Methodological rigor was assessed using the relevant Critical Appraisal Skills Programme tool. RESULTS: Nine articles were included. Contextual factors, which helped implementation, included the CYP having a high perception of need for a PHR and a high level of desire for self‐management. Service providers and CYP need knowledge about the purpose and benefits of the PHR, and organisations need a dedicated person to facilitate PHR use. Mechanisms triggered by the PHR included improved understanding and knowledge of health care condition(s) for CYP, an increased feeling of control over condition(s), and more active engagement in their health care. Outcomes for CYP included improved self‐advocacy and communication. CONCLUSION: Clearer definitions of which young people would benefit from using a PHR must be established to inform which organisations and service providers would be best suited to PHR implementation. John Wiley and Sons Inc. 2019-04-03 2019-05 /pmc/articles/PMC6519173/ /pubmed/30817012 http://dx.doi.org/10.1111/cch.12652 Text en © 2019 The Authors. Child: Care, Health and Development published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Articles Diffin, Janet Byrne, Bronagh Kerr, Helen Price, Jayne Abbott, Aine McLaughlin, Dorry O'Halloran, Peter The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature |
title | The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature |
title_full | The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature |
title_fullStr | The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature |
title_full_unstemmed | The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature |
title_short | The usefulness and acceptability of a personal health record to children and young people living with a complex health condition: A realist review of the literature |
title_sort | usefulness and acceptability of a personal health record to children and young people living with a complex health condition: a realist review of the literature |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519173/ https://www.ncbi.nlm.nih.gov/pubmed/30817012 http://dx.doi.org/10.1111/cch.12652 |
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