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Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools
BACKGROUND: Measurement of patients’ healthcare experiences is increasingly used as an indicator of quality of care, but there are concerns that existing measures omit information that is meaningful to patients and that results may not be used systematically to inform service improvement. Further, c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042987/ https://www.ncbi.nlm.nih.gov/pubmed/33845852 http://dx.doi.org/10.1186/s12939-021-01433-2 |
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author | Green, Monica Cunningham, Joan Anderson, Kate Griffiths, Kalinda Garvey, Gail |
author_facet | Green, Monica Cunningham, Joan Anderson, Kate Griffiths, Kalinda Garvey, Gail |
author_sort | Green, Monica |
collection | PubMed |
description | BACKGROUND: Measurement of patients’ healthcare experiences is increasingly used as an indicator of quality of care, but there are concerns that existing measures omit information that is meaningful to patients and that results may not be used systematically to inform service improvement. Further, current approaches may be inadequate for some population groups, such as Indigenous people in Australia, whose healthcare experience is impacted by the context of colonisation and discordance between Indigenous understandings of health and the Western biomedical health system. This study aimed to assess the extent to which existing patient experience measures used in Australia collect information about critical aspects of cancer care, as previously identified by Indigenous people affected by cancer and their health care providers. METHODS: A two-stage process was used to examine the adequacy of existing patient experience measures for Indigenous people in Australia: (1) relevant tools and measures were identified and assessed, and four measures selected as suitable comparators; (2) comparators were examined in detail and mapped against topics identified in earlier research as important to Indigenous people with cancer. Gaps in topic coverage in comparators were identified. RESULTS: No comparators completely captured the critical aspects of cancer care identified by Indigenous people affected by cancer and their health care providers. The number of topics ‘partially’ captured by the four comparators ranged from 4 to 7 out of 9. While most topics were partially covered, the lack of questions around culture and cultural safety was notable. CONCLUSIONS: Existing tools are likely to miss key aspects of Indigenous peoples’ experiences of cancer care in Australia. Failure to adequately assess care experiences related to cultural safety may compromise efforts to improve health outcomes. Addressing gaps requires development of experience measures that are strengths-based, reflect an Indigenous worldview and measure aspects of experience relevant to Indigenous people. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12939-021-01433-2. |
format | Online Article Text |
id | pubmed-8042987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80429872021-04-14 Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools Green, Monica Cunningham, Joan Anderson, Kate Griffiths, Kalinda Garvey, Gail Int J Equity Health Research BACKGROUND: Measurement of patients’ healthcare experiences is increasingly used as an indicator of quality of care, but there are concerns that existing measures omit information that is meaningful to patients and that results may not be used systematically to inform service improvement. Further, current approaches may be inadequate for some population groups, such as Indigenous people in Australia, whose healthcare experience is impacted by the context of colonisation and discordance between Indigenous understandings of health and the Western biomedical health system. This study aimed to assess the extent to which existing patient experience measures used in Australia collect information about critical aspects of cancer care, as previously identified by Indigenous people affected by cancer and their health care providers. METHODS: A two-stage process was used to examine the adequacy of existing patient experience measures for Indigenous people in Australia: (1) relevant tools and measures were identified and assessed, and four measures selected as suitable comparators; (2) comparators were examined in detail and mapped against topics identified in earlier research as important to Indigenous people with cancer. Gaps in topic coverage in comparators were identified. RESULTS: No comparators completely captured the critical aspects of cancer care identified by Indigenous people affected by cancer and their health care providers. The number of topics ‘partially’ captured by the four comparators ranged from 4 to 7 out of 9. While most topics were partially covered, the lack of questions around culture and cultural safety was notable. CONCLUSIONS: Existing tools are likely to miss key aspects of Indigenous peoples’ experiences of cancer care in Australia. Failure to adequately assess care experiences related to cultural safety may compromise efforts to improve health outcomes. Addressing gaps requires development of experience measures that are strengths-based, reflect an Indigenous worldview and measure aspects of experience relevant to Indigenous people. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12939-021-01433-2. BioMed Central 2021-04-12 /pmc/articles/PMC8042987/ /pubmed/33845852 http://dx.doi.org/10.1186/s12939-021-01433-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Green, Monica Cunningham, Joan Anderson, Kate Griffiths, Kalinda Garvey, Gail Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools |
title | Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools |
title_full | Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools |
title_fullStr | Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools |
title_full_unstemmed | Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools |
title_short | Measuring health care experiences that matter to Indigenous people in Australia with cancer: identifying critical gaps in existing tools |
title_sort | measuring health care experiences that matter to indigenous people in australia with cancer: identifying critical gaps in existing tools |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042987/ https://www.ncbi.nlm.nih.gov/pubmed/33845852 http://dx.doi.org/10.1186/s12939-021-01433-2 |
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