A systematic literature review of the assessment of treatment burden experienced by patients and their caregivers
Autor: | Bruce Leff, Debra Saliba, Orla C. Sheehan, Roya Fathi, Cynthia M. Boyd, Lingsheng Li, Sarah K. Garrigues, Christine S. Ritchie |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Treatment burden
medicine.medical_specialty Health Personnel Population Scopus Qualitative property CINAHL Cochrane Library lcsh:Geriatrics 03 medical and health sciences 0302 clinical medicine Cost of Illness Surveys and Questionnaires Humans Medicine 030212 general & internal medicine education Qualitative Research education.field_of_study Patient business.industry Caregiver lcsh:RC952-954.6 Treatment Outcome Systematic review Caregivers Patient Satisfaction Multiple chronic conditions 030220 oncology & carcinogenesis Family medicine Chronic Disease Geriatrics and Gerontology business Research Article Qualitative research |
Zdroj: | BMC Geriatrics, Vol 19, Iss 1, Pp 1-11 (2019) BMC Geriatrics |
ISSN: | 1471-2318 |
Popis: | 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. |
Databáze: | OpenAIRE |
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