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The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases
Introduction The assessment of using patient‐reported outcomes (PROs) within comprehensive care follow‐up programmes, specifically focused on health screening, remains largely unexplored. PROs were implemented in our late effects and comprehensive care programme after paediatric hematopoietic stem c...
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Published in: | Health expectations : an international journal of public participation in health care and health policy 2024-02, Vol.27 (1), p.e13902-n/a |
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creator | Bense, Joëll E. Guilonard, Nicole Zwaginga, Femke Stiggelbout, Anne M. Louwerens, Marloes Mekelenkamp, Hilda Lankester, Arjan C. Pieterse, Arwen H. Pagter, Anne P. J. |
description | Introduction
The assessment of using patient‐reported outcomes (PROs) within comprehensive care follow‐up programmes, specifically focused on health screening, remains largely unexplored. PROs were implemented in our late effects and comprehensive care programme after paediatric hematopoietic stem cell transplantation (HSCT) for nonmalignant diseases. The programme focuses solely on screening of physical and mental health and on discussing PROs during the consultation.
Methods
The primary method of this study was semistructured interviews to explore the perspective of both patients and healthcare providers' (HCP) on the use of PROs, which were thematically analyzed. Additionally, an explorative quantitative approach with patient‐reported experience measures (PREMS) was used, with a pretest–posttest design, to assess whether the use of PROs was accompanied by more patient‐centred care.
Results
From the patient‐interviews (N = 15) four themes were extracted: use of PROs (1) help to discuss topics; (2) make the patients feel understood; (3) create a moment of self‐reflection; and (4) make consultations more efficient. Pre‐ and postimplementation analysis of PREMs (N = 40) did not show significant differences in terms of patient‐centeredness.
Conclusion
Our results demonstrate the added value of integrating PROs for health screening purposes within the long‐term follow‐up programme after paediatric HSCT, as perceived by both patient and HCP. With the active use of PROs, patients are stimulated to consciously assess their health status.
Patient Contribution
This study included patients as participants. Caregivers were approached if patients were below a certain age. Additionally, preliminary results were shared with all patients (including nonparticipants) during a patient conference day. |
doi_str_mv | 10.1111/hex.13902 |
format | article |
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The assessment of using patient‐reported outcomes (PROs) within comprehensive care follow‐up programmes, specifically focused on health screening, remains largely unexplored. PROs were implemented in our late effects and comprehensive care programme after paediatric hematopoietic stem cell transplantation (HSCT) for nonmalignant diseases. The programme focuses solely on screening of physical and mental health and on discussing PROs during the consultation.
Methods
The primary method of this study was semistructured interviews to explore the perspective of both patients and healthcare providers' (HCP) on the use of PROs, which were thematically analyzed. Additionally, an explorative quantitative approach with patient‐reported experience measures (PREMS) was used, with a pretest–posttest design, to assess whether the use of PROs was accompanied by more patient‐centred care.
Results
From the patient‐interviews (N = 15) four themes were extracted: use of PROs (1) help to discuss topics; (2) make the patients feel understood; (3) create a moment of self‐reflection; and (4) make consultations more efficient. Pre‐ and postimplementation analysis of PREMs (N = 40) did not show significant differences in terms of patient‐centeredness.
Conclusion
Our results demonstrate the added value of integrating PROs for health screening purposes within the long‐term follow‐up programme after paediatric HSCT, as perceived by both patient and HCP. With the active use of PROs, patients are stimulated to consciously assess their health status.
Patient Contribution
This study included patients as participants. Caregivers were approached if patients were below a certain age. Additionally, preliminary results were shared with all patients (including nonparticipants) during a patient conference day.</description><identifier>ISSN: 1369-6513</identifier><identifier>ISSN: 1369-7625</identifier><identifier>EISSN: 1369-7625</identifier><identifier>DOI: 10.1111/hex.13902</identifier><identifier>PMID: 38102818</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adolescent ; Adult ; Bone marrow ; Caregivers ; Child ; Child, Preschool ; Clinical outcomes ; Data collection ; Disease ; Female ; Follow-Up Studies ; health screening ; Health status ; Hematopoietic Stem Cell Transplantation ; Hematopoietic stem cells ; Humans ; Interviews ; Interviews as Topic ; Long term ; Male ; Mass Screening ; Medical research ; Medical screening ; Mental health ; Outpatient care facilities ; Patient Reported Outcome Measures ; Patient-Centered Care ; Patients ; patient‐centred care ; patient‐reported experience ; patient‐reported outcomes ; Pediatrics ; Psychological assessment ; Questionnaires ; Selfreflection ; Stem cell transplantation ; Stem cells ; Transplantation ; Transplants ; value‐based healthcare</subject><ispartof>Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13902-n/a</ispartof><rights>2023 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2023 The Authors. Health Expectations published by John Wiley & Sons Ltd.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4142-c6a1d46d1fd52d1c68973afbd377c9901346c42a8db32f8c8e521a948f74a02f3</cites><orcidid>0000-0002-7051-1872 ; 0000-0002-7939-334X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2931050714/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2931050714?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,11543,12827,25734,27905,27906,30980,36993,36994,44571,46033,46457,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38102818$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bense, Joëll E.</creatorcontrib><creatorcontrib>Guilonard, Nicole</creatorcontrib><creatorcontrib>Zwaginga, Femke</creatorcontrib><creatorcontrib>Stiggelbout, Anne M.</creatorcontrib><creatorcontrib>Louwerens, Marloes</creatorcontrib><creatorcontrib>Mekelenkamp, Hilda</creatorcontrib><creatorcontrib>Lankester, Arjan C.</creatorcontrib><creatorcontrib>Pieterse, Arwen H.</creatorcontrib><creatorcontrib>Pagter, Anne P. J.</creatorcontrib><title>The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases</title><title>Health expectations : an international journal of public participation in health care and health policy</title><addtitle>Health Expect</addtitle><description>Introduction
The assessment of using patient‐reported outcomes (PROs) within comprehensive care follow‐up programmes, specifically focused on health screening, remains largely unexplored. PROs were implemented in our late effects and comprehensive care programme after paediatric hematopoietic stem cell transplantation (HSCT) for nonmalignant diseases. The programme focuses solely on screening of physical and mental health and on discussing PROs during the consultation.
Methods
The primary method of this study was semistructured interviews to explore the perspective of both patients and healthcare providers' (HCP) on the use of PROs, which were thematically analyzed. Additionally, an explorative quantitative approach with patient‐reported experience measures (PREMS) was used, with a pretest–posttest design, to assess whether the use of PROs was accompanied by more patient‐centred care.
Results
From the patient‐interviews (N = 15) four themes were extracted: use of PROs (1) help to discuss topics; (2) make the patients feel understood; (3) create a moment of self‐reflection; and (4) make consultations more efficient. Pre‐ and postimplementation analysis of PREMs (N = 40) did not show significant differences in terms of patient‐centeredness.
Conclusion
Our results demonstrate the added value of integrating PROs for health screening purposes within the long‐term follow‐up programme after paediatric HSCT, as perceived by both patient and HCP. With the active use of PROs, patients are stimulated to consciously assess their health status.
Patient Contribution
This study included patients as participants. Caregivers were approached if patients were below a certain age. Additionally, preliminary results were shared with all patients (including nonparticipants) during a patient conference day.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Bone marrow</subject><subject>Caregivers</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Clinical outcomes</subject><subject>Data collection</subject><subject>Disease</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>health screening</subject><subject>Health status</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hematopoietic stem cells</subject><subject>Humans</subject><subject>Interviews</subject><subject>Interviews as Topic</subject><subject>Long term</subject><subject>Male</subject><subject>Mass Screening</subject><subject>Medical research</subject><subject>Medical screening</subject><subject>Mental health</subject><subject>Outpatient care facilities</subject><subject>Patient Reported Outcome Measures</subject><subject>Patient-Centered Care</subject><subject>Patients</subject><subject>patient‐centred care</subject><subject>patient‐reported experience</subject><subject>patient‐reported outcomes</subject><subject>Pediatrics</subject><subject>Psychological assessment</subject><subject>Questionnaires</subject><subject>Selfreflection</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Transplantation</subject><subject>Transplants</subject><subject>value‐based healthcare</subject><issn>1369-6513</issn><issn>1369-7625</issn><issn>1369-7625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>7QJ</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kktuFDEQQFsIREJgwQWQJTawmMS_7nYvURRIpEhsgsSuVWNXz3jkthvbnZBdjpBbcC9OgudDFkh4U3bp-flTVVVvGT1lZZyt8ecpEx3lz6pjJppu0Ta8fn6YNzUTR9WrlDaUslao9mV1JBSjXDF1XP26WSO5BTcjCQOZk_UrMkG26PPvh8eIU4gZDQlz1mHERIYQyRrB5TVJOiL67QYzx21wwa_KpoxxLJxz4a6s5onAUFLFisZCjlaTlHEkGp0jOYJPkwOfy5nB7_Q--BGcXfmSJcYmhITpdfViAJfwzSGeVN8-X9ycXy6uv365Ov90vdCSSb7QDTAjG8MGU3PDdKO6VsCwNKJtdddRJmSjJQdlloIPSiusOYNOqqGVQPkgTqqrvdcE2PRTtCPE-z6A7XeJEFc9xGy1w77jStTlG8G0nWwBlF52nCpeTlvWkvHi-rB3TTH8mDHlfrRp-2zwGObU81KxTlKpREHf_4Nuwhx9eWmhBKM1bZks1Mc9pWNIKeLwdEFG-20n9KUT-l0nFPbdwTgvRzRP5N_SF-BsD9xZh_f_N_WXF9_3yj-2lcLz</recordid><startdate>202402</startdate><enddate>202402</enddate><creator>Bense, Joëll E.</creator><creator>Guilonard, Nicole</creator><creator>Zwaginga, Femke</creator><creator>Stiggelbout, Anne M.</creator><creator>Louwerens, Marloes</creator><creator>Mekelenkamp, Hilda</creator><creator>Lankester, Arjan C.</creator><creator>Pieterse, Arwen H.</creator><creator>Pagter, Anne P. J.</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</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>3V.</scope><scope>7QJ</scope><scope>7RV</scope><scope>7T2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7051-1872</orcidid><orcidid>https://orcid.org/0000-0002-7939-334X</orcidid></search><sort><creationdate>202402</creationdate><title>The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases</title><author>Bense, Joëll E. ; Guilonard, Nicole ; Zwaginga, Femke ; Stiggelbout, Anne M. ; Louwerens, Marloes ; Mekelenkamp, Hilda ; Lankester, Arjan C. ; Pieterse, Arwen H. ; Pagter, Anne P. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4142-c6a1d46d1fd52d1c68973afbd377c9901346c42a8db32f8c8e521a948f74a02f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Bone marrow</topic><topic>Caregivers</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clinical outcomes</topic><topic>Data collection</topic><topic>Disease</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>health screening</topic><topic>Health status</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic stem cells</topic><topic>Humans</topic><topic>Interviews</topic><topic>Interviews as Topic</topic><topic>Long term</topic><topic>Male</topic><topic>Mass Screening</topic><topic>Medical research</topic><topic>Medical screening</topic><topic>Mental health</topic><topic>Outpatient care facilities</topic><topic>Patient Reported Outcome Measures</topic><topic>Patient-Centered Care</topic><topic>Patients</topic><topic>patient‐centred care</topic><topic>patient‐reported experience</topic><topic>patient‐reported outcomes</topic><topic>Pediatrics</topic><topic>Psychological assessment</topic><topic>Questionnaires</topic><topic>Selfreflection</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Transplantation</topic><topic>Transplants</topic><topic>value‐based healthcare</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bense, Joëll E.</creatorcontrib><creatorcontrib>Guilonard, Nicole</creatorcontrib><creatorcontrib>Zwaginga, Femke</creatorcontrib><creatorcontrib>Stiggelbout, Anne M.</creatorcontrib><creatorcontrib>Louwerens, Marloes</creatorcontrib><creatorcontrib>Mekelenkamp, Hilda</creatorcontrib><creatorcontrib>Lankester, Arjan C.</creatorcontrib><creatorcontrib>Pieterse, Arwen H.</creatorcontrib><creatorcontrib>Pagter, Anne P. 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J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases</atitle><jtitle>Health expectations : an international journal of public participation in health care and health policy</jtitle><addtitle>Health Expect</addtitle><date>2024-02</date><risdate>2024</risdate><volume>27</volume><issue>1</issue><spage>e13902</spage><epage>n/a</epage><pages>e13902-n/a</pages><issn>1369-6513</issn><issn>1369-7625</issn><eissn>1369-7625</eissn><abstract>Introduction
The assessment of using patient‐reported outcomes (PROs) within comprehensive care follow‐up programmes, specifically focused on health screening, remains largely unexplored. PROs were implemented in our late effects and comprehensive care programme after paediatric hematopoietic stem cell transplantation (HSCT) for nonmalignant diseases. The programme focuses solely on screening of physical and mental health and on discussing PROs during the consultation.
Methods
The primary method of this study was semistructured interviews to explore the perspective of both patients and healthcare providers' (HCP) on the use of PROs, which were thematically analyzed. Additionally, an explorative quantitative approach with patient‐reported experience measures (PREMS) was used, with a pretest–posttest design, to assess whether the use of PROs was accompanied by more patient‐centred care.
Results
From the patient‐interviews (N = 15) four themes were extracted: use of PROs (1) help to discuss topics; (2) make the patients feel understood; (3) create a moment of self‐reflection; and (4) make consultations more efficient. Pre‐ and postimplementation analysis of PREMs (N = 40) did not show significant differences in terms of patient‐centeredness.
Conclusion
Our results demonstrate the added value of integrating PROs for health screening purposes within the long‐term follow‐up programme after paediatric HSCT, as perceived by both patient and HCP. With the active use of PROs, patients are stimulated to consciously assess their health status.
Patient Contribution
This study included patients as participants. Caregivers were approached if patients were below a certain age. Additionally, preliminary results were shared with all patients (including nonparticipants) during a patient conference day.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>38102818</pmid><doi>10.1111/hex.13902</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7051-1872</orcidid><orcidid>https://orcid.org/0000-0002-7939-334X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Bone marrow Caregivers Child Child, Preschool Clinical outcomes Data collection Disease Female Follow-Up Studies health screening Health status Hematopoietic Stem Cell Transplantation Hematopoietic stem cells Humans Interviews Interviews as Topic Long term Male Mass Screening Medical research Medical screening Mental health Outpatient care facilities Patient Reported Outcome Measures Patient-Centered Care Patients patient‐centred care patient‐reported experience patient‐reported outcomes Pediatrics Psychological assessment Questionnaires Selfreflection Stem cell transplantation Stem cells Transplantation Transplants value‐based healthcare |
title | The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases |
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