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When the patient is the expert: measuring patient experience and satisfaction with care
In 2018, three independent reports were published, emphasizing the need for attention to, and improvements in, quality of care to achieve effective universal health coverage. A key aspect of high quality health care and health systems is that they are person-centred, a characteristic that is at the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Health Organization
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6653815/ https://www.ncbi.nlm.nih.gov/pubmed/31384074 http://dx.doi.org/10.2471/BLT.18.225201 |
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author | Larson, Elysia Sharma, Jigyasa Bohren, Meghan A Tunçalp, Özge |
author_facet | Larson, Elysia Sharma, Jigyasa Bohren, Meghan A Tunçalp, Özge |
author_sort | Larson, Elysia |
collection | PubMed |
description | In 2018, three independent reports were published, emphasizing the need for attention to, and improvements in, quality of care to achieve effective universal health coverage. A key aspect of high quality health care and health systems is that they are person-centred, a characteristic that is at the same time intrinsically important (all individuals have the right to be treated with dignity and respect) and instrumentally important (person-centred care is associated with improved health-care utilization and health outcomes). Following calls to make 2019 a year of action, we provide guidance to policy-makers, researchers and implementers on how they can take on the task of measuring person-centred care. Theoretically, measures of person-centred care allow quality improvement efforts to be evaluated and ensure that health systems are accountable to those they aim to serve. However, in practice, the utility of these measures is limited by lack of clarity and precision in designing and by using measures for different aspects of person-centeredness. We discuss the distinction between two broad categories of measures of patient-centred care: patient experience and patient satisfaction. We frame our discussion of these measures around three key questions: (i) how will the results of this measure be used?; (ii) how will patient subjectivity be accounted for?; and (iii) is this measure validated or tested? By addressing these issues during the design phase, researchers will increase the usability of their measures. |
format | Online Article Text |
id | pubmed-6653815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | World Health Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-66538152019-08-06 When the patient is the expert: measuring patient experience and satisfaction with care Larson, Elysia Sharma, Jigyasa Bohren, Meghan A Tunçalp, Özge Bull World Health Organ Policy & Practice In 2018, three independent reports were published, emphasizing the need for attention to, and improvements in, quality of care to achieve effective universal health coverage. A key aspect of high quality health care and health systems is that they are person-centred, a characteristic that is at the same time intrinsically important (all individuals have the right to be treated with dignity and respect) and instrumentally important (person-centred care is associated with improved health-care utilization and health outcomes). Following calls to make 2019 a year of action, we provide guidance to policy-makers, researchers and implementers on how they can take on the task of measuring person-centred care. Theoretically, measures of person-centred care allow quality improvement efforts to be evaluated and ensure that health systems are accountable to those they aim to serve. However, in practice, the utility of these measures is limited by lack of clarity and precision in designing and by using measures for different aspects of person-centeredness. We discuss the distinction between two broad categories of measures of patient-centred care: patient experience and patient satisfaction. We frame our discussion of these measures around three key questions: (i) how will the results of this measure be used?; (ii) how will patient subjectivity be accounted for?; and (iii) is this measure validated or tested? By addressing these issues during the design phase, researchers will increase the usability of their measures. World Health Organization 2019-08-01 2019-05-28 /pmc/articles/PMC6653815/ /pubmed/31384074 http://dx.doi.org/10.2471/BLT.18.225201 Text en (c) 2019 The authors; licensee World Health Organization. This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL. |
spellingShingle | Policy & Practice Larson, Elysia Sharma, Jigyasa Bohren, Meghan A Tunçalp, Özge When the patient is the expert: measuring patient experience and satisfaction with care |
title | When the patient is the expert: measuring patient experience and satisfaction with care |
title_full | When the patient is the expert: measuring patient experience and satisfaction with care |
title_fullStr | When the patient is the expert: measuring patient experience and satisfaction with care |
title_full_unstemmed | When the patient is the expert: measuring patient experience and satisfaction with care |
title_short | When the patient is the expert: measuring patient experience and satisfaction with care |
title_sort | when the patient is the expert: measuring patient experience and satisfaction with care |
topic | Policy & Practice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6653815/ https://www.ncbi.nlm.nih.gov/pubmed/31384074 http://dx.doi.org/10.2471/BLT.18.225201 |
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