Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Palliative medicine 2022-01, Vol.36 (1), p.124-134
Main Authors: Guo, Ping, Pinto, Cathryn, Edwards, Beth, Pask, Sophie, Firth, Alice, O’Brien, Suzanne, Murtagh, Fliss EM
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353
cites cdi_FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353
container_end_page 134
container_issue 1
container_start_page 124
container_title Palliative medicine
container_volume 36
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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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>
fulltext fulltext
identifier ISSN: 0269-2163
ispartof Palliative medicine, 2022-01, Vol.36 (1), p.124-134
issn 0269-2163
1477-030X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8793309
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A21%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Experiences%20of%20transitioning%20between%20settings%20of%20care%20from%20the%20perspectives%20of%20patients%20with%20advanced%20illness%20receiving%20specialist%20palliative%20care%20and%20their%20family%20caregivers:%20A%20qualitative%20interview%20study&rft.jtitle=Palliative%20medicine&rft.au=Guo,%20Ping&rft.date=2022-01-01&rft.volume=36&rft.issue=1&rft.spage=124&rft.epage=134&rft.pages=124-134&rft.issn=0269-2163&rft.eissn=1477-030X&rft_id=info:doi/10.1177/02692163211043371&rft_dat=%3Cproquest_pubme%3E2622758444%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c466t-b1860144d3a9cf6c49b958a8ad7f59ebd8785b3b1fce89257b8debb9ecc77353%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2622758444&rft_id=info:pmid/34477022&rft_sage_id=10.1177_02692163211043371&rfr_iscdi=true