The key actor : A qualitative study of patient participation in the handover process in Europe

Background: Patient safety experts have postulated that increasing patient participation in communications during patient handovers will improve the quality of patient transitions, and that this may reduce hospital readmissions. Choosing strategies that enhance patient safety through improved handov...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Flink, Maria, Hesselink, Gijs, Pijnenborg, Loes, Wollersheim, Hub, Vernooij-Dassen, Myrra, Dudzik-Urbaniak, Ewa, Orrego, Carola, Toccafondi, Giulio, Schoonhoven, Lisette, Gademan, Petra J, Johnson, Julie K, Oḧlén, Gunnar, Hansagi, Helen, Olsson, Mariann, Barach, Paul
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator Flink, Maria
Hesselink, Gijs
Pijnenborg, Loes
Wollersheim, Hub
Vernooij-Dassen, Myrra
Dudzik-Urbaniak, Ewa
Orrego, Carola
Toccafondi, Giulio
Schoonhoven, Lisette
Gademan, Petra J
Johnson, Julie K
Oḧlén, Gunnar
Hansagi, Helen
Olsson, Mariann
Barach, Paul
description Background: Patient safety experts have postulated that increasing patient participation in communications during patient handovers will improve the quality of patient transitions, and that this may reduce hospital readmissions. Choosing strategies that enhance patient safety through improved handovers requires better understanding of patient experiences and preferences for participation. Objective: The aim of this paper is to explore the patients' experiences and perspectives related to the handovers between their primary care providers and the inpatient hospital. Methods: A qualitative secondary analysis was performed, based on individual and focus group patient interviews with 90 patients in five European countries. Results: The analysis revealed three themes: patient positioning in the handover process; prerequisites for patient participation and patient preferences for the handover process. Patients' participation ranged from being the key actor, to sharing the responsibility with healthcare professional(s), to being passive participants. For active participation patients required both personal and social resources as well as prerequisites such as information and respect. Some patients preferred to be the key actor in charge; others preferred their healthcare professionals to be the key actors in the handover. Conclusions: Patients' participation is related to the healthcare system, the activity of healthcare professionals' and patients' capacity for participation. Patients prefer a handover process where the responsibility is clear and unambiguous. Healthcare organisations need a clear and well-considered system of responsibility for handover processes, that takes into account the individual patient's need of clarity, and support in relation to his/hers own recourses.
format Article
fullrecord <record><control><sourceid>csuc_XX2</sourceid><recordid>TN_cdi_csuc_recercat_oai_recercat_cat_2072_530054</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_recercat_cat_2072_530054</sourcerecordid><originalsourceid>FETCH-csuc_recercat_oai_recercat_cat_2072_5300543</originalsourceid><addsrcrecordid>eNqdi8EKglAQRd20iOof5gcC0yRoF2H0Aa6TYRzxobyxefME_z6FoH2Ly-FcONvkVXUMPc-AZKJwhRu8Iw7O0NzEECw2M0gL4-LsbaGaI7eqeHAebOk79I1MrDCqEIew_mVUGXmfbFocAh--3CWnR1ndn0cKkWplYiW0WtD9ZF2WXrK6yNO0OOf_NB_GO0kx</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The key actor : A qualitative study of patient participation in the handover process in Europe</title><source>Recercat</source><creator>Flink, Maria ; Hesselink, Gijs ; Pijnenborg, Loes ; Wollersheim, Hub ; Vernooij-Dassen, Myrra ; Dudzik-Urbaniak, Ewa ; Orrego, Carola ; Toccafondi, Giulio ; Schoonhoven, Lisette ; Gademan, Petra J ; Johnson, Julie K ; Oḧlén, Gunnar ; Hansagi, Helen ; Olsson, Mariann ; Barach, Paul</creator><creatorcontrib>Flink, Maria ; Hesselink, Gijs ; Pijnenborg, Loes ; Wollersheim, Hub ; Vernooij-Dassen, Myrra ; Dudzik-Urbaniak, Ewa ; Orrego, Carola ; Toccafondi, Giulio ; Schoonhoven, Lisette ; Gademan, Petra J ; Johnson, Julie K ; Oḧlén, Gunnar ; Hansagi, Helen ; Olsson, Mariann ; Barach, Paul</creatorcontrib><description>Background: Patient safety experts have postulated that increasing patient participation in communications during patient handovers will improve the quality of patient transitions, and that this may reduce hospital readmissions. Choosing strategies that enhance patient safety through improved handovers requires better understanding of patient experiences and preferences for participation. Objective: The aim of this paper is to explore the patients' experiences and perspectives related to the handovers between their primary care providers and the inpatient hospital. Methods: A qualitative secondary analysis was performed, based on individual and focus group patient interviews with 90 patients in five European countries. Results: The analysis revealed three themes: patient positioning in the handover process; prerequisites for patient participation and patient preferences for the handover process. Patients' participation ranged from being the key actor, to sharing the responsibility with healthcare professional(s), to being passive participants. For active participation patients required both personal and social resources as well as prerequisites such as information and respect. Some patients preferred to be the key actor in charge; others preferred their healthcare professionals to be the key actors in the handover. Conclusions: Patients' participation is related to the healthcare system, the activity of healthcare professionals' and patients' capacity for participation. Patients prefer a handover process where the responsibility is clear and unambiguous. Healthcare organisations need a clear and well-considered system of responsibility for handover processes, that takes into account the individual patient's need of clarity, and support in relation to his/hers own recourses.</description><language>eng</language><subject>Chronic Disease ; European Union ; Female ; Focus Groups ; General Practitioners ; Health Knowledge, Attitudes, Practice ; Humans ; Interviews as Topic ; Male ; Patient Handoff ; Patient Participation ; Patient Safety ; Patient Satisfaction ; Patients ; Physician-Patient Relations ; Qualitative Research ; Quality Assurance, Health Care</subject><creationdate>2012</creationdate><rights>open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by-nc/4.0</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,777,882,26955</link.rule.ids><linktorsrc>$$Uhttps://recercat.cat/handle/2072/530054$$EView_record_in_Consorci_de_Serveis_Universitaris_de_Catalunya_(CSUC)$$FView_record_in_$$GConsorci_de_Serveis_Universitaris_de_Catalunya_(CSUC)$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Flink, Maria</creatorcontrib><creatorcontrib>Hesselink, Gijs</creatorcontrib><creatorcontrib>Pijnenborg, Loes</creatorcontrib><creatorcontrib>Wollersheim, Hub</creatorcontrib><creatorcontrib>Vernooij-Dassen, Myrra</creatorcontrib><creatorcontrib>Dudzik-Urbaniak, Ewa</creatorcontrib><creatorcontrib>Orrego, Carola</creatorcontrib><creatorcontrib>Toccafondi, Giulio</creatorcontrib><creatorcontrib>Schoonhoven, Lisette</creatorcontrib><creatorcontrib>Gademan, Petra J</creatorcontrib><creatorcontrib>Johnson, Julie K</creatorcontrib><creatorcontrib>Oḧlén, Gunnar</creatorcontrib><creatorcontrib>Hansagi, Helen</creatorcontrib><creatorcontrib>Olsson, Mariann</creatorcontrib><creatorcontrib>Barach, Paul</creatorcontrib><title>The key actor : A qualitative study of patient participation in the handover process in Europe</title><description>Background: Patient safety experts have postulated that increasing patient participation in communications during patient handovers will improve the quality of patient transitions, and that this may reduce hospital readmissions. Choosing strategies that enhance patient safety through improved handovers requires better understanding of patient experiences and preferences for participation. Objective: The aim of this paper is to explore the patients' experiences and perspectives related to the handovers between their primary care providers and the inpatient hospital. Methods: A qualitative secondary analysis was performed, based on individual and focus group patient interviews with 90 patients in five European countries. Results: The analysis revealed three themes: patient positioning in the handover process; prerequisites for patient participation and patient preferences for the handover process. Patients' participation ranged from being the key actor, to sharing the responsibility with healthcare professional(s), to being passive participants. For active participation patients required both personal and social resources as well as prerequisites such as information and respect. Some patients preferred to be the key actor in charge; others preferred their healthcare professionals to be the key actors in the handover. Conclusions: Patients' participation is related to the healthcare system, the activity of healthcare professionals' and patients' capacity for participation. Patients prefer a handover process where the responsibility is clear and unambiguous. Healthcare organisations need a clear and well-considered system of responsibility for handover processes, that takes into account the individual patient's need of clarity, and support in relation to his/hers own recourses.</description><subject>Chronic Disease</subject><subject>European Union</subject><subject>Female</subject><subject>Focus Groups</subject><subject>General Practitioners</subject><subject>Health Knowledge, Attitudes, Practice</subject><subject>Humans</subject><subject>Interviews as Topic</subject><subject>Male</subject><subject>Patient Handoff</subject><subject>Patient Participation</subject><subject>Patient Safety</subject><subject>Patient Satisfaction</subject><subject>Patients</subject><subject>Physician-Patient Relations</subject><subject>Qualitative Research</subject><subject>Quality Assurance, Health Care</subject><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>XX2</sourceid><recordid>eNqdi8EKglAQRd20iOof5gcC0yRoF2H0Aa6TYRzxobyxefME_z6FoH2Ly-FcONvkVXUMPc-AZKJwhRu8Iw7O0NzEECw2M0gL4-LsbaGaI7eqeHAebOk79I1MrDCqEIew_mVUGXmfbFocAh--3CWnR1ndn0cKkWplYiW0WtD9ZF2WXrK6yNO0OOf_NB_GO0kx</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Flink, Maria</creator><creator>Hesselink, Gijs</creator><creator>Pijnenborg, Loes</creator><creator>Wollersheim, Hub</creator><creator>Vernooij-Dassen, Myrra</creator><creator>Dudzik-Urbaniak, Ewa</creator><creator>Orrego, Carola</creator><creator>Toccafondi, Giulio</creator><creator>Schoonhoven, Lisette</creator><creator>Gademan, Petra J</creator><creator>Johnson, Julie K</creator><creator>Oḧlén, Gunnar</creator><creator>Hansagi, Helen</creator><creator>Olsson, Mariann</creator><creator>Barach, Paul</creator><scope>XX2</scope></search><sort><creationdate>2012</creationdate><title>The key actor : A qualitative study of patient participation in the handover process in Europe</title><author>Flink, Maria ; Hesselink, Gijs ; Pijnenborg, Loes ; Wollersheim, Hub ; Vernooij-Dassen, Myrra ; Dudzik-Urbaniak, Ewa ; Orrego, Carola ; Toccafondi, Giulio ; Schoonhoven, Lisette ; Gademan, Petra J ; Johnson, Julie K ; Oḧlén, Gunnar ; Hansagi, Helen ; Olsson, Mariann ; Barach, Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-csuc_recercat_oai_recercat_cat_2072_5300543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Chronic Disease</topic><topic>European Union</topic><topic>Female</topic><topic>Focus Groups</topic><topic>General Practitioners</topic><topic>Health Knowledge, Attitudes, Practice</topic><topic>Humans</topic><topic>Interviews as Topic</topic><topic>Male</topic><topic>Patient Handoff</topic><topic>Patient Participation</topic><topic>Patient Safety</topic><topic>Patient Satisfaction</topic><topic>Patients</topic><topic>Physician-Patient Relations</topic><topic>Qualitative Research</topic><topic>Quality Assurance, Health Care</topic><toplevel>online_resources</toplevel><creatorcontrib>Flink, Maria</creatorcontrib><creatorcontrib>Hesselink, Gijs</creatorcontrib><creatorcontrib>Pijnenborg, Loes</creatorcontrib><creatorcontrib>Wollersheim, Hub</creatorcontrib><creatorcontrib>Vernooij-Dassen, Myrra</creatorcontrib><creatorcontrib>Dudzik-Urbaniak, Ewa</creatorcontrib><creatorcontrib>Orrego, Carola</creatorcontrib><creatorcontrib>Toccafondi, Giulio</creatorcontrib><creatorcontrib>Schoonhoven, Lisette</creatorcontrib><creatorcontrib>Gademan, Petra J</creatorcontrib><creatorcontrib>Johnson, Julie K</creatorcontrib><creatorcontrib>Oḧlén, Gunnar</creatorcontrib><creatorcontrib>Hansagi, Helen</creatorcontrib><creatorcontrib>Olsson, Mariann</creatorcontrib><creatorcontrib>Barach, Paul</creatorcontrib><collection>Recercat</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Flink, Maria</au><au>Hesselink, Gijs</au><au>Pijnenborg, Loes</au><au>Wollersheim, Hub</au><au>Vernooij-Dassen, Myrra</au><au>Dudzik-Urbaniak, Ewa</au><au>Orrego, Carola</au><au>Toccafondi, Giulio</au><au>Schoonhoven, Lisette</au><au>Gademan, Petra J</au><au>Johnson, Julie K</au><au>Oḧlén, Gunnar</au><au>Hansagi, Helen</au><au>Olsson, Mariann</au><au>Barach, Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The key actor : A qualitative study of patient participation in the handover process in Europe</atitle><date>2012</date><risdate>2012</risdate><abstract>Background: Patient safety experts have postulated that increasing patient participation in communications during patient handovers will improve the quality of patient transitions, and that this may reduce hospital readmissions. Choosing strategies that enhance patient safety through improved handovers requires better understanding of patient experiences and preferences for participation. Objective: The aim of this paper is to explore the patients' experiences and perspectives related to the handovers between their primary care providers and the inpatient hospital. Methods: A qualitative secondary analysis was performed, based on individual and focus group patient interviews with 90 patients in five European countries. Results: The analysis revealed three themes: patient positioning in the handover process; prerequisites for patient participation and patient preferences for the handover process. Patients' participation ranged from being the key actor, to sharing the responsibility with healthcare professional(s), to being passive participants. For active participation patients required both personal and social resources as well as prerequisites such as information and respect. Some patients preferred to be the key actor in charge; others preferred their healthcare professionals to be the key actors in the handover. Conclusions: Patients' participation is related to the healthcare system, the activity of healthcare professionals' and patients' capacity for participation. Patients prefer a handover process where the responsibility is clear and unambiguous. Healthcare organisations need a clear and well-considered system of responsibility for handover processes, that takes into account the individual patient's need of clarity, and support in relation to his/hers own recourses.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_csuc_recercat_oai_recercat_cat_2072_530054
source Recercat
subjects Chronic Disease
European Union
Female
Focus Groups
General Practitioners
Health Knowledge, Attitudes, Practice
Humans
Interviews as Topic
Male
Patient Handoff
Patient Participation
Patient Safety
Patient Satisfaction
Patients
Physician-Patient Relations
Qualitative Research
Quality Assurance, Health Care
title The key actor : A qualitative study of patient participation in the handover process in Europe
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T22%3A21%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-csuc_XX2&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20key%20actor%20:%20A%20qualitative%20study%20of%20patient%20participation%20in%20the%20handover%20process%20in%20Europe&rft.au=Flink,%20Maria&rft.date=2012&rft_id=info:doi/&rft_dat=%3Ccsuc_XX2%3Eoai_recercat_cat_2072_530054%3C/csuc_XX2%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true