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A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers
BACKGROUND: Many older adults with multiple chronic conditions, particularly those who are functionally impaired, spend considerable time juggling the competing demands of managing their conditions often assisted by caregivers. We examined methods of assessing the treatment burden experienced by thi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788093/ https://www.ncbi.nlm.nih.gov/pubmed/31604424 http://dx.doi.org/10.1186/s12877-019-1222-z |
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author | Sheehan, Orla C. Leff, Bruce Ritchie, Christine S. Garrigues, Sarah K. Li, Lingsheng Saliba, Debra Fathi, Roya Boyd, Cynthia M. |
author_facet | Sheehan, Orla C. Leff, Bruce Ritchie, Christine S. Garrigues, Sarah K. Li, Lingsheng Saliba, Debra Fathi, Roya Boyd, Cynthia M. |
author_sort | Sheehan, Orla C. |
collection | PubMed |
description | BACKGROUND: Many older adults with multiple chronic conditions, particularly those who are functionally impaired, spend considerable time juggling the competing demands of managing their conditions often assisted by caregivers. We examined methods of assessing the treatment burden experienced by this population as a first step to identifying strategies to reduce it. METHODS: Systematic searches were performed of the peer-reviewed and grey-literature (PubMed, Cochrane library, CINAHL, EMBASE, Web of Science, SCOPUS, New York Academy of Medicine Grey Literature Review, NLM catalog and ProQuest Digital Theses and Dissertations). After title and abstract screening, both qualitative and quantitative articles describing approaches to assessment of treatment burden were included. RESULTS: Forty-five articles from the peer reviewed and three items from the grey literature were identified. Most articles (34/48) discussed treatment burden associated with a specific condition. All but one examined the treatment burden experienced by patients and six addressed the treatment burden experienced by caregivers. Qualitative studies revealed many aspects of treatment burden including the burdens of understanding the condition, juggling, monitoring and adjusting treatments, efforts to engage with others for support as well as financial and time burdens. Many tools to assess treatment burden in different populations were identified through the qualitative data. The most commonly used instrument was the Treatment Burden Questionnaire. CONCLUSIONS: Many instruments are available to assess treatment burden, but no one standardized assessment method was identified. Few articles examined approaches to measuring the treatment burden experienced by caregivers. As people live longer with more chronic conditions healthcare providers need to identify patients and caregivers burdened by treatment and engage in approaches to ameliorate treatment burden. A standard and validated assessment method to measure treatment burden in the clinical setting would help to enhance the care of people with multiple chronic conditions, allow comparison of different approaches to reducing treatment burden, and foster ongoing evaluation and monitoring of burden across conditions, patient populations, and time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12877-019-1222-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6788093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67880932019-10-18 A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers Sheehan, Orla C. Leff, Bruce Ritchie, Christine S. Garrigues, Sarah K. Li, Lingsheng Saliba, Debra Fathi, Roya Boyd, Cynthia M. BMC Geriatr Research Article BACKGROUND: Many older adults with multiple chronic conditions, particularly those who are functionally impaired, spend considerable time juggling the competing demands of managing their conditions often assisted by caregivers. We examined methods of assessing the treatment burden experienced by this population as a first step to identifying strategies to reduce it. METHODS: Systematic searches were performed of the peer-reviewed and grey-literature (PubMed, Cochrane library, CINAHL, EMBASE, Web of Science, SCOPUS, New York Academy of Medicine Grey Literature Review, NLM catalog and ProQuest Digital Theses and Dissertations). After title and abstract screening, both qualitative and quantitative articles describing approaches to assessment of treatment burden were included. RESULTS: Forty-five articles from the peer reviewed and three items from the grey literature were identified. Most articles (34/48) discussed treatment burden associated with a specific condition. All but one examined the treatment burden experienced by patients and six addressed the treatment burden experienced by caregivers. Qualitative studies revealed many aspects of treatment burden including the burdens of understanding the condition, juggling, monitoring and adjusting treatments, efforts to engage with others for support as well as financial and time burdens. Many tools to assess treatment burden in different populations were identified through the qualitative data. The most commonly used instrument was the Treatment Burden Questionnaire. CONCLUSIONS: Many instruments are available to assess treatment burden, but no one standardized assessment method was identified. Few articles examined approaches to measuring the treatment burden experienced by caregivers. As people live longer with more chronic conditions healthcare providers need to identify patients and caregivers burdened by treatment and engage in approaches to ameliorate treatment burden. A standard and validated assessment method to measure treatment burden in the clinical setting would help to enhance the care of people with multiple chronic conditions, allow comparison of different approaches to reducing treatment burden, and foster ongoing evaluation and monitoring of burden across conditions, patient populations, and time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12877-019-1222-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-10-11 /pmc/articles/PMC6788093/ /pubmed/31604424 http://dx.doi.org/10.1186/s12877-019-1222-z 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 | Research Article Sheehan, Orla C. Leff, Bruce Ritchie, Christine S. Garrigues, Sarah K. Li, Lingsheng Saliba, Debra Fathi, Roya Boyd, Cynthia M. A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
title | A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
title_full | A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
title_fullStr | A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
title_full_unstemmed | A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
title_short | A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
title_sort | systematic literature review of the assessment of treatment burden experienced by patients and their caregivers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788093/ https://www.ncbi.nlm.nih.gov/pubmed/31604424 http://dx.doi.org/10.1186/s12877-019-1222-z |
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