Symptom Management Assistance from Unpaid and Family Caregivers to Older Adults in the Last Month of Life (GP733)

Outcomes. 1. Know the size of the population of family caregivers experiencing difficulty in managing symptoms at the end of life 2. Know the extent to which caregivers experience difficulty in managing symptoms at the end of life 3. Describe factors associated with report of difficulty in managing...

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Veröffentlicht in:Journal of pain and symptom management 2022-06, Vol.63 (6), p.1130
Hauptverfasser: Mather, Harriet, Ornstein, Katherine, Bollens-Lund, Evan, Kleijwegt, Hannah, Kelley, Amy
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container_end_page
container_issue 6
container_start_page 1130
container_title Journal of pain and symptom management
container_volume 63
creator Mather, Harriet
Ornstein, Katherine
Bollens-Lund, Evan
Kleijwegt, Hannah
Kelley, Amy
description Outcomes. 1. Know the size of the population of family caregivers experiencing difficulty in managing symptoms at the end of life 2. Know the extent to which caregivers experience difficulty in managing symptoms at the end of life 3. Describe factors associated with report of difficulty in managing symptoms at the end of life Importance. The recommendations of the federal Recognize, Assist, Include, Support and Engage Family Caregiving Advisory Council highlighted the need to support and train caregivers in symptom management at the end of life. Planning implementation of such programs requires an estimate of the size of the caregiver population experiencing difficulty managing common symptoms (e.g., pain, dyspnea, anxiety) and characterization of factors associated with difficulty in a nationally representative sample. Objective(s). Provide a population-weighted estimate of the size of caregiver population reporting difficulty in managing symptoms at the end of life and examine patient and caregiver factors associated with reports of difficulty in managing symptoms at the end of life. Method(s). We conducted a cross-sectional analysis of data from the nationally representative National Study of Caregiving III and the National Health and Aging Trends Study from 2017. We calculated a population estimate of caregivers reporting any difficulty in managing pain, dyspnea, or anxiety in the last month of life. We used bivariate and multivariable analyses to examine the association between caregiver sociodemographic characteristics, caregiving circumstances, care recipient factors, and reports of any symptom management difficulty. Results. The study sample included 254 caregivers of community-dwelling older adults in the last month of life, representing 2.3 million caregivers nationally (45.3% daughters, 15.4% spouses; 85.7% non-Hispanic White). Overall, 87.4% (2 million) caregivers provided support managing symptoms; 78% (1.6 million) reported difficulty. Of those who reported managing pain, dyspnea, and anxiety, 82.0%, 71.1%, and 88.3%, respectively, reported difficulty. In multivariable mixed effect regression models, caregiver education greater than high school and number of care recipient comorbidities were significantly associated with caregiver reports of difficulty managing symptoms. Conclusion(s). End-of-life symptom management is challenging for caregivers, with anxiety being the most challenging symptom to manage. Impact. This study reinforces the call
doi_str_mv 10.1016/j.jpainsymman.2022.04.124
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Know the size of the population of family caregivers experiencing difficulty in managing symptoms at the end of life 2. Know the extent to which caregivers experience difficulty in managing symptoms at the end of life 3. Describe factors associated with report of difficulty in managing symptoms at the end of life Importance. The recommendations of the federal Recognize, Assist, Include, Support and Engage Family Caregiving Advisory Council highlighted the need to support and train caregivers in symptom management at the end of life. Planning implementation of such programs requires an estimate of the size of the caregiver population experiencing difficulty managing common symptoms (e.g., pain, dyspnea, anxiety) and characterization of factors associated with difficulty in a nationally representative sample. Objective(s). Provide a population-weighted estimate of the size of caregiver population reporting difficulty in managing symptoms at the end of life and examine patient and caregiver factors associated with reports of difficulty in managing symptoms at the end of life. Method(s). We conducted a cross-sectional analysis of data from the nationally representative National Study of Caregiving III and the National Health and Aging Trends Study from 2017. We calculated a population estimate of caregivers reporting any difficulty in managing pain, dyspnea, or anxiety in the last month of life. We used bivariate and multivariable analyses to examine the association between caregiver sociodemographic characteristics, caregiving circumstances, care recipient factors, and reports of any symptom management difficulty. Results. The study sample included 254 caregivers of community-dwelling older adults in the last month of life, representing 2.3 million caregivers nationally (45.3% daughters, 15.4% spouses; 85.7% non-Hispanic White). Overall, 87.4% (2 million) caregivers provided support managing symptoms; 78% (1.6 million) reported difficulty. Of those who reported managing pain, dyspnea, and anxiety, 82.0%, 71.1%, and 88.3%, respectively, reported difficulty. In multivariable mixed effect regression models, caregiver education greater than high school and number of care recipient comorbidities were significantly associated with caregiver reports of difficulty managing symptoms. Conclusion(s). End-of-life symptom management is challenging for caregivers, with anxiety being the most challenging symptom to manage. Impact. This study reinforces the call for further education and support for caregivers managing symptoms at the end of life.</description><identifier>ISSN: 0885-3924</identifier><identifier>DOI: 10.1016/j.jpainsymman.2022.04.124</identifier><language>eng</language><publisher>Madison: Elsevier Limited</publisher><subject>Aging ; Anxiety ; Caregivers ; Caregiving ; Continuing education ; Daughters ; Dyspnea ; End of life decisions ; Older people ; Pain ; Population ; Secondary schools ; Sociodemographics ; Spouses ; Symptom management ; Symptoms ; Unpaid</subject><ispartof>Journal of pain and symptom management, 2022-06, Vol.63 (6), p.1130</ispartof><rights>Copyright Elsevier Limited Jun 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904,30978</link.rule.ids></links><search><creatorcontrib>Mather, Harriet</creatorcontrib><creatorcontrib>Ornstein, Katherine</creatorcontrib><creatorcontrib>Bollens-Lund, Evan</creatorcontrib><creatorcontrib>Kleijwegt, Hannah</creatorcontrib><creatorcontrib>Kelley, Amy</creatorcontrib><title>Symptom Management Assistance from Unpaid and Family Caregivers to Older Adults in the Last Month of Life (GP733)</title><title>Journal of pain and symptom management</title><description>Outcomes. 1. Know the size of the population of family caregivers experiencing difficulty in managing symptoms at the end of life 2. Know the extent to which caregivers experience difficulty in managing symptoms at the end of life 3. Describe factors associated with report of difficulty in managing symptoms at the end of life Importance. The recommendations of the federal Recognize, Assist, Include, Support and Engage Family Caregiving Advisory Council highlighted the need to support and train caregivers in symptom management at the end of life. Planning implementation of such programs requires an estimate of the size of the caregiver population experiencing difficulty managing common symptoms (e.g., pain, dyspnea, anxiety) and characterization of factors associated with difficulty in a nationally representative sample. Objective(s). Provide a population-weighted estimate of the size of caregiver population reporting difficulty in managing symptoms at the end of life and examine patient and caregiver factors associated with reports of difficulty in managing symptoms at the end of life. Method(s). We conducted a cross-sectional analysis of data from the nationally representative National Study of Caregiving III and the National Health and Aging Trends Study from 2017. We calculated a population estimate of caregivers reporting any difficulty in managing pain, dyspnea, or anxiety in the last month of life. We used bivariate and multivariable analyses to examine the association between caregiver sociodemographic characteristics, caregiving circumstances, care recipient factors, and reports of any symptom management difficulty. Results. The study sample included 254 caregivers of community-dwelling older adults in the last month of life, representing 2.3 million caregivers nationally (45.3% daughters, 15.4% spouses; 85.7% non-Hispanic White). Overall, 87.4% (2 million) caregivers provided support managing symptoms; 78% (1.6 million) reported difficulty. Of those who reported managing pain, dyspnea, and anxiety, 82.0%, 71.1%, and 88.3%, respectively, reported difficulty. In multivariable mixed effect regression models, caregiver education greater than high school and number of care recipient comorbidities were significantly associated with caregiver reports of difficulty managing symptoms. Conclusion(s). End-of-life symptom management is challenging for caregivers, with anxiety being the most challenging symptom to manage. Impact. 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Know the size of the population of family caregivers experiencing difficulty in managing symptoms at the end of life 2. Know the extent to which caregivers experience difficulty in managing symptoms at the end of life 3. Describe factors associated with report of difficulty in managing symptoms at the end of life Importance. The recommendations of the federal Recognize, Assist, Include, Support and Engage Family Caregiving Advisory Council highlighted the need to support and train caregivers in symptom management at the end of life. Planning implementation of such programs requires an estimate of the size of the caregiver population experiencing difficulty managing common symptoms (e.g., pain, dyspnea, anxiety) and characterization of factors associated with difficulty in a nationally representative sample. Objective(s). Provide a population-weighted estimate of the size of caregiver population reporting difficulty in managing symptoms at the end of life and examine patient and caregiver factors associated with reports of difficulty in managing symptoms at the end of life. Method(s). We conducted a cross-sectional analysis of data from the nationally representative National Study of Caregiving III and the National Health and Aging Trends Study from 2017. We calculated a population estimate of caregivers reporting any difficulty in managing pain, dyspnea, or anxiety in the last month of life. We used bivariate and multivariable analyses to examine the association between caregiver sociodemographic characteristics, caregiving circumstances, care recipient factors, and reports of any symptom management difficulty. Results. The study sample included 254 caregivers of community-dwelling older adults in the last month of life, representing 2.3 million caregivers nationally (45.3% daughters, 15.4% spouses; 85.7% non-Hispanic White). Overall, 87.4% (2 million) caregivers provided support managing symptoms; 78% (1.6 million) reported difficulty. Of those who reported managing pain, dyspnea, and anxiety, 82.0%, 71.1%, and 88.3%, respectively, reported difficulty. In multivariable mixed effect regression models, caregiver education greater than high school and number of care recipient comorbidities were significantly associated with caregiver reports of difficulty managing symptoms. Conclusion(s). End-of-life symptom management is challenging for caregivers, with anxiety being the most challenging symptom to manage. Impact. This study reinforces the call for further education and support for caregivers managing symptoms at the end of life.</abstract><cop>Madison</cop><pub>Elsevier Limited</pub><doi>10.1016/j.jpainsymman.2022.04.124</doi><oa>free_for_read</oa></addata></record>
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source Applied Social Sciences Index & Abstracts (ASSIA); Elsevier ScienceDirect Journals Complete
subjects Aging
Anxiety
Caregivers
Caregiving
Continuing education
Daughters
Dyspnea
End of life decisions
Older people
Pain
Population
Secondary schools
Sociodemographics
Spouses
Symptom management
Symptoms
Unpaid
title Symptom Management Assistance from Unpaid and Family Caregivers to Older Adults in the Last Month of Life (GP733)
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