Cargando…
A systematic review of dimensions evaluating patient experience in chronic illness
BACKGROUND: Living with a chronic disease often means experiencing chronic treatments and regular multidisciplinary monitoring as well as a profound life-changing experience which may impact all aspects of a patients life. The patient experience of chronic disease is frequently assessed by patient r...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341593/ https://www.ncbi.nlm.nih.gov/pubmed/30665417 http://dx.doi.org/10.1186/s12955-019-1084-2 |
_version_ | 1783388971858919424 |
---|---|
author | Forestier, Bastien Anthoine, Emmanuelle Reguiai, Ziad Fohrer, Cécile Blanchin, Myriam |
author_facet | Forestier, Bastien Anthoine, Emmanuelle Reguiai, Ziad Fohrer, Cécile Blanchin, Myriam |
author_sort | Forestier, Bastien |
collection | PubMed |
description | BACKGROUND: Living with a chronic disease often means experiencing chronic treatments and regular multidisciplinary monitoring as well as a profound life-changing experience which may impact all aspects of a patients life. The patient experience of chronic disease is frequently assessed by patient reported measures (PRMs) which incorporate patients perspectives to better understand how illness, treatment and care impact the entirety of a patient’s life. The purpose of this review was to collect and review different kinds of available PRM instruments validated for chronic patients, to produce an inventory of explored concepts in these questionnaires and to identify and classify all dimensions assessing chronic patients experience. METHODS: A systematic review of PRM instruments validated for chronic patients was conducted from three databases (Medline, the Cochrane library, and Psycinfo). Articles were selected after a double reading and questionnaires were classified according to their targeted concept. Then, all dimensions of the questionnaires were clustered into different categories. RESULTS: 107 primary validation studies of PRM questionnaires were selected. Five kinds of instruments were recorded: 1) Questionnaires assessing health related quality of life or quality of life; 2) Instruments focusing on symptoms and functional status; 3) Instruments exploring patients’ feelings and attitude about illness; 4) Questionnaires related to patients’ experience of treatment or healthcare; 5) Instruments assessing patients attitudes about treatment or healthcare. Twelve categories of dimensions were obtained from these instruments. CONCLUSIONS: This review provided an overview of some of the dimensions used to explore chronic patient experience. A large PRM diversity exists and none of the reviewed and selected questionnaires covered all identified categories of dimensions of patient experience of chronic disease. Furthermore, the definition of explored concepts varies widely among researchers and complex concepts often lack a clear definition in the reviewed articles. Before attempting to measure chronic patient experience, researchers should construct appropriate instruments focusing on well-defined concepts and dimensions encompassing patient’s personal experience, attitude and adaptation to illness, treatment or healthcare. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12955-019-1084-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6341593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63415932019-01-24 A systematic review of dimensions evaluating patient experience in chronic illness Forestier, Bastien Anthoine, Emmanuelle Reguiai, Ziad Fohrer, Cécile Blanchin, Myriam Health Qual Life Outcomes Review BACKGROUND: Living with a chronic disease often means experiencing chronic treatments and regular multidisciplinary monitoring as well as a profound life-changing experience which may impact all aspects of a patients life. The patient experience of chronic disease is frequently assessed by patient reported measures (PRMs) which incorporate patients perspectives to better understand how illness, treatment and care impact the entirety of a patient’s life. The purpose of this review was to collect and review different kinds of available PRM instruments validated for chronic patients, to produce an inventory of explored concepts in these questionnaires and to identify and classify all dimensions assessing chronic patients experience. METHODS: A systematic review of PRM instruments validated for chronic patients was conducted from three databases (Medline, the Cochrane library, and Psycinfo). Articles were selected after a double reading and questionnaires were classified according to their targeted concept. Then, all dimensions of the questionnaires were clustered into different categories. RESULTS: 107 primary validation studies of PRM questionnaires were selected. Five kinds of instruments were recorded: 1) Questionnaires assessing health related quality of life or quality of life; 2) Instruments focusing on symptoms and functional status; 3) Instruments exploring patients’ feelings and attitude about illness; 4) Questionnaires related to patients’ experience of treatment or healthcare; 5) Instruments assessing patients attitudes about treatment or healthcare. Twelve categories of dimensions were obtained from these instruments. CONCLUSIONS: This review provided an overview of some of the dimensions used to explore chronic patient experience. A large PRM diversity exists and none of the reviewed and selected questionnaires covered all identified categories of dimensions of patient experience of chronic disease. Furthermore, the definition of explored concepts varies widely among researchers and complex concepts often lack a clear definition in the reviewed articles. Before attempting to measure chronic patient experience, researchers should construct appropriate instruments focusing on well-defined concepts and dimensions encompassing patient’s personal experience, attitude and adaptation to illness, treatment or healthcare. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12955-019-1084-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-21 /pmc/articles/PMC6341593/ /pubmed/30665417 http://dx.doi.org/10.1186/s12955-019-1084-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Review Forestier, Bastien Anthoine, Emmanuelle Reguiai, Ziad Fohrer, Cécile Blanchin, Myriam A systematic review of dimensions evaluating patient experience in chronic illness |
title | A systematic review of dimensions evaluating patient experience in chronic illness |
title_full | A systematic review of dimensions evaluating patient experience in chronic illness |
title_fullStr | A systematic review of dimensions evaluating patient experience in chronic illness |
title_full_unstemmed | A systematic review of dimensions evaluating patient experience in chronic illness |
title_short | A systematic review of dimensions evaluating patient experience in chronic illness |
title_sort | systematic review of dimensions evaluating patient experience in chronic illness |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341593/ https://www.ncbi.nlm.nih.gov/pubmed/30665417 http://dx.doi.org/10.1186/s12955-019-1084-2 |
work_keys_str_mv | AT forestierbastien asystematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT anthoineemmanuelle asystematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT reguiaiziad asystematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT fohrercecile asystematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT blanchinmyriam asystematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT forestierbastien systematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT anthoineemmanuelle systematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT reguiaiziad systematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT fohrercecile systematicreviewofdimensionsevaluatingpatientexperienceinchronicillness AT blanchinmyriam systematicreviewofdimensionsevaluatingpatientexperienceinchronicillness |