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Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview study
Background: Transitions between care settings (hospice, hospital and community) can be challenging for patients and family caregivers and are often an under-researched area of health care, including palliative care. Aim: To explore the experience of transitions between care settings for those receiv...
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Published in: | Palliative medicine 2022-01, Vol.36 (1), p.124-134 |
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creator | Guo, Ping Pinto, Cathryn Edwards, Beth Pask, Sophie Firth, Alice O’Brien, Suzanne Murtagh, Fliss EM |
description | Background:
Transitions between care settings (hospice, hospital and community) can be challenging for patients and family caregivers and are often an under-researched area of health care, including palliative care.
Aim:
To explore the experience of transitions between care settings for those receiving specialist palliative care.
Design:
Qualitative study using thematic analysis.
Setting/participants:
Semi-structured interviews were conducted with adult patients (n = 15) and family caregivers (n = 11) receiving specialist palliative care, who had undergone at least two transitions.
Results:
Four themes were identified. (1) Uncertainty about the new care setting. Most participants reported that lack of information about the new setting of care, and difficulties with access and availability of care in the new setting, added to feelings of uncertainty. (2) Biographical disruption. The transition to the new setting often resulted in changes to sense of independence and identity, and maintaining normality was a way to cope with this. (3) Importance of continuity of care. Continuity of care had an impact on feelings of safety in the new setting and influenced decisions about the transition. (4) Need for emotional and practical support. Most participants expressed a greater need for emotional and practical support, when transitioning to a new setting.
Conclusions:
Findings provide insights into how clinicians might better negotiate transitions for these patients and family caregivers, as well as improve patient outcomes. The complexity and diversity of transition experiences, particularly among patients and families from different ethnicities and cultural backgrounds, need to be further explored in future research. |
doi_str_mv | 10.1177/02692163211043371 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8793309</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_02692163211043371</sage_id><sourcerecordid>2622758444</sourcerecordid><originalsourceid>FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353</originalsourceid><addsrcrecordid>eNp1kstu1DAUhiMEokPhAdggS2zYpNixEzsskKqqXKRKbLpgZ9nOyYwrx5naToZ5SN4JpynlJlaWfb7_Oz7SKYqXBJ8RwvlbXDVtRRpaEYIZpZw8KjaEcV5iir8-LjZLvVyAk-JZjDcYE4ob9rQ4oSxTuKo2xffLb3sIFryBiMYepaB8tMmO3vot0pAOAB5FSCnf7wijAqA-jANKO0A5HPdgkp3X_F6lLEsRHWzaIdXNKps7ZJ3zECMKYMDOi3pJWeVsTDnjnFWLYpUr3y1uG1CvBuuOd6_bXA7xHTpHt1OOpZW3PkGYLRxQTFN3fF486ZWL8OL-PC2uP1xeX3wqr758_HxxflUa1jSp1EQ0mDDWUdWavjGs1W0tlFAd7-sWdCe4qDXVpDcg2qrmWnSgdQvGcE5relq8X7X7SQ_QmTxwUE7ugx1UOMpRWflnxdud3I6zFLylFLdZ8OZeEMbbCWKSg40GnFMexinKqm5aKhgVS6_Xf6E34xR8nk5WTVXxWjDGMkVWyoQxxgD9w2cIlsuuyH92JWde_T7FQ-LncmTgbAWi2sKvtv83_gBPnc6b</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2622758444</pqid></control><display><type>article</type><title>Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview study</title><source>Applied Social Sciences Index & Abstracts (ASSIA)</source><source>SAGE</source><creator>Guo, Ping ; Pinto, Cathryn ; Edwards, Beth ; Pask, Sophie ; Firth, Alice ; O’Brien, Suzanne ; Murtagh, Fliss EM</creator><creatorcontrib>Guo, Ping ; Pinto, Cathryn ; Edwards, Beth ; Pask, Sophie ; Firth, Alice ; O’Brien, Suzanne ; Murtagh, Fliss EM</creatorcontrib><description>Background:
Transitions between care settings (hospice, hospital and community) can be challenging for patients and family caregivers and are often an under-researched area of health care, including palliative care.
Aim:
To explore the experience of transitions between care settings for those receiving specialist palliative care.
Design:
Qualitative study using thematic analysis.
Setting/participants:
Semi-structured interviews were conducted with adult patients (n = 15) and family caregivers (n = 11) receiving specialist palliative care, who had undergone at least two transitions.
Results:
Four themes were identified. (1) Uncertainty about the new care setting. Most participants reported that lack of information about the new setting of care, and difficulties with access and availability of care in the new setting, added to feelings of uncertainty. (2) Biographical disruption. The transition to the new setting often resulted in changes to sense of independence and identity, and maintaining normality was a way to cope with this. (3) Importance of continuity of care. Continuity of care had an impact on feelings of safety in the new setting and influenced decisions about the transition. (4) Need for emotional and practical support. Most participants expressed a greater need for emotional and practical support, when transitioning to a new setting.
Conclusions:
Findings provide insights into how clinicians might better negotiate transitions for these patients and family caregivers, as well as improve patient outcomes. The complexity and diversity of transition experiences, particularly among patients and families from different ethnicities and cultural backgrounds, need to be further explored in future research.</description><identifier>ISSN: 0269-2163</identifier><identifier>EISSN: 1477-030X</identifier><identifier>DOI: 10.1177/02692163211043371</identifier><identifier>PMID: 34477022</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Adult ; Caregivers ; Caregivers - psychology ; Clinical outcomes ; Continuity of care ; Cultural differences ; Disruption ; Family - psychology ; Health care ; Hospice Care ; Hospices ; Humans ; Interviews ; Multiculturalism & pluralism ; Normality ; Original ; Palliative care ; Palliative Care - psychology ; Qualitative Research ; Transitions ; Uncertainty</subject><ispartof>Palliative medicine, 2022-01, Vol.36 (1), p.124-134</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021 2021 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353</citedby><cites>FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353</cites><orcidid>0000-0003-0726-0502 ; 0000-0003-0979-7047 ; 0000-0001-6152-1940 ; 0000-0003-1289-3726</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925,30999,79236</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34477022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Ping</creatorcontrib><creatorcontrib>Pinto, Cathryn</creatorcontrib><creatorcontrib>Edwards, Beth</creatorcontrib><creatorcontrib>Pask, Sophie</creatorcontrib><creatorcontrib>Firth, Alice</creatorcontrib><creatorcontrib>O’Brien, Suzanne</creatorcontrib><creatorcontrib>Murtagh, Fliss EM</creatorcontrib><title>Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview study</title><title>Palliative medicine</title><addtitle>Palliat Med</addtitle><description>Background:
Transitions between care settings (hospice, hospital and community) can be challenging for patients and family caregivers and are often an under-researched area of health care, including palliative care.
Aim:
To explore the experience of transitions between care settings for those receiving specialist palliative care.
Design:
Qualitative study using thematic analysis.
Setting/participants:
Semi-structured interviews were conducted with adult patients (n = 15) and family caregivers (n = 11) receiving specialist palliative care, who had undergone at least two transitions.
Results:
Four themes were identified. (1) Uncertainty about the new care setting. Most participants reported that lack of information about the new setting of care, and difficulties with access and availability of care in the new setting, added to feelings of uncertainty. (2) Biographical disruption. The transition to the new setting often resulted in changes to sense of independence and identity, and maintaining normality was a way to cope with this. (3) Importance of continuity of care. Continuity of care had an impact on feelings of safety in the new setting and influenced decisions about the transition. (4) Need for emotional and practical support. Most participants expressed a greater need for emotional and practical support, when transitioning to a new setting.
Conclusions:
Findings provide insights into how clinicians might better negotiate transitions for these patients and family caregivers, as well as improve patient outcomes. The complexity and diversity of transition experiences, particularly among patients and families from different ethnicities and cultural backgrounds, need to be further explored in future research.</description><subject>Adult</subject><subject>Caregivers</subject><subject>Caregivers - psychology</subject><subject>Clinical outcomes</subject><subject>Continuity of care</subject><subject>Cultural differences</subject><subject>Disruption</subject><subject>Family - psychology</subject><subject>Health care</subject><subject>Hospice Care</subject><subject>Hospices</subject><subject>Humans</subject><subject>Interviews</subject><subject>Multiculturalism & pluralism</subject><subject>Normality</subject><subject>Original</subject><subject>Palliative care</subject><subject>Palliative Care - psychology</subject><subject>Qualitative Research</subject><subject>Transitions</subject><subject>Uncertainty</subject><issn>0269-2163</issn><issn>1477-030X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>7QJ</sourceid><recordid>eNp1kstu1DAUhiMEokPhAdggS2zYpNixEzsskKqqXKRKbLpgZ9nOyYwrx5naToZ5SN4JpynlJlaWfb7_Oz7SKYqXBJ8RwvlbXDVtRRpaEYIZpZw8KjaEcV5iir8-LjZLvVyAk-JZjDcYE4ob9rQ4oSxTuKo2xffLb3sIFryBiMYepaB8tMmO3vot0pAOAB5FSCnf7wijAqA-jANKO0A5HPdgkp3X_F6lLEsRHWzaIdXNKps7ZJ3zECMKYMDOi3pJWeVsTDnjnFWLYpUr3y1uG1CvBuuOd6_bXA7xHTpHt1OOpZW3PkGYLRxQTFN3fF486ZWL8OL-PC2uP1xeX3wqr758_HxxflUa1jSp1EQ0mDDWUdWavjGs1W0tlFAd7-sWdCe4qDXVpDcg2qrmWnSgdQvGcE5relq8X7X7SQ_QmTxwUE7ugx1UOMpRWflnxdud3I6zFLylFLdZ8OZeEMbbCWKSg40GnFMexinKqm5aKhgVS6_Xf6E34xR8nk5WTVXxWjDGMkVWyoQxxgD9w2cIlsuuyH92JWde_T7FQ-LncmTgbAWi2sKvtv83_gBPnc6b</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Guo, Ping</creator><creator>Pinto, Cathryn</creator><creator>Edwards, Beth</creator><creator>Pask, Sophie</creator><creator>Firth, Alice</creator><creator>O’Brien, Suzanne</creator><creator>Murtagh, Fliss EM</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>ASE</scope><scope>FPQ</scope><scope>K6X</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0726-0502</orcidid><orcidid>https://orcid.org/0000-0003-0979-7047</orcidid><orcidid>https://orcid.org/0000-0001-6152-1940</orcidid><orcidid>https://orcid.org/0000-0003-1289-3726</orcidid></search><sort><creationdate>20220101</creationdate><title>Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview study</title><author>Guo, Ping ; Pinto, Cathryn ; Edwards, Beth ; Pask, Sophie ; Firth, Alice ; O’Brien, Suzanne ; Murtagh, Fliss EM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Caregivers</topic><topic>Caregivers - psychology</topic><topic>Clinical outcomes</topic><topic>Continuity of care</topic><topic>Cultural differences</topic><topic>Disruption</topic><topic>Family - psychology</topic><topic>Health care</topic><topic>Hospice Care</topic><topic>Hospices</topic><topic>Humans</topic><topic>Interviews</topic><topic>Multiculturalism & pluralism</topic><topic>Normality</topic><topic>Original</topic><topic>Palliative care</topic><topic>Palliative Care - psychology</topic><topic>Qualitative Research</topic><topic>Transitions</topic><topic>Uncertainty</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Ping</creatorcontrib><creatorcontrib>Pinto, Cathryn</creatorcontrib><creatorcontrib>Edwards, Beth</creatorcontrib><creatorcontrib>Pask, Sophie</creatorcontrib><creatorcontrib>Firth, Alice</creatorcontrib><creatorcontrib>O’Brien, Suzanne</creatorcontrib><creatorcontrib>Murtagh, Fliss EM</creatorcontrib><collection>SAGE Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Palliative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Ping</au><au>Pinto, Cathryn</au><au>Edwards, Beth</au><au>Pask, Sophie</au><au>Firth, Alice</au><au>O’Brien, Suzanne</au><au>Murtagh, Fliss EM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview study</atitle><jtitle>Palliative medicine</jtitle><addtitle>Palliat Med</addtitle><date>2022-01-01</date><risdate>2022</risdate><volume>36</volume><issue>1</issue><spage>124</spage><epage>134</epage><pages>124-134</pages><issn>0269-2163</issn><eissn>1477-030X</eissn><abstract>Background:
Transitions between care settings (hospice, hospital and community) can be challenging for patients and family caregivers and are often an under-researched area of health care, including palliative care.
Aim:
To explore the experience of transitions between care settings for those receiving specialist palliative care.
Design:
Qualitative study using thematic analysis.
Setting/participants:
Semi-structured interviews were conducted with adult patients (n = 15) and family caregivers (n = 11) receiving specialist palliative care, who had undergone at least two transitions.
Results:
Four themes were identified. (1) Uncertainty about the new care setting. Most participants reported that lack of information about the new setting of care, and difficulties with access and availability of care in the new setting, added to feelings of uncertainty. (2) Biographical disruption. The transition to the new setting often resulted in changes to sense of independence and identity, and maintaining normality was a way to cope with this. (3) Importance of continuity of care. Continuity of care had an impact on feelings of safety in the new setting and influenced decisions about the transition. (4) Need for emotional and practical support. Most participants expressed a greater need for emotional and practical support, when transitioning to a new setting.
Conclusions:
Findings provide insights into how clinicians might better negotiate transitions for these patients and family caregivers, as well as improve patient outcomes. The complexity and diversity of transition experiences, particularly among patients and families from different ethnicities and cultural backgrounds, need to be further explored in future research.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>34477022</pmid><doi>10.1177/02692163211043371</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0726-0502</orcidid><orcidid>https://orcid.org/0000-0003-0979-7047</orcidid><orcidid>https://orcid.org/0000-0001-6152-1940</orcidid><orcidid>https://orcid.org/0000-0003-1289-3726</orcidid><oa>free_for_read</oa></addata></record> |
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ispartof | Palliative medicine, 2022-01, Vol.36 (1), p.124-134 |
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source | Applied Social Sciences Index & Abstracts (ASSIA); SAGE |
subjects | Adult Caregivers Caregivers - psychology Clinical outcomes Continuity of care Cultural differences Disruption Family - psychology Health care Hospice Care Hospices Humans Interviews Multiculturalism & pluralism Normality Original Palliative care Palliative Care - psychology Qualitative Research Transitions Uncertainty |
title | Experiences of transitioning between settings of care from the perspectives of patients with advanced illness receiving specialist palliative care and their family caregivers: A qualitative interview study |
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