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Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol

INTRODUCTION: An electronic Patient-Reported Outcome (ePRO) platform is needed for implementing evidence-based symptom management in outpatients with advanced cancer. We describe the overall protocol and the methodology for measuring symptom burden, to provide critical parameters needed to implement...

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Autores principales: Tang, Lili, Pang, Ying, He, Yi, Shi, Qiuling, Han, Xinkun, Li, Zimeng, Zhou, Chengcheng, Zhou, Yuhe, He, Shuangzhi, Wang, Yan, Zhang, Yening, Song, Lili, Wang, Bingmei, Li, Xiumin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682447/
https://www.ncbi.nlm.nih.gov/pubmed/33444183
http://dx.doi.org/10.1136/bmjopen-2020-038223
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author Tang, Lili
Pang, Ying
He, Yi
Shi, Qiuling
Han, Xinkun
Li, Zimeng
Zhou, Chengcheng
Zhou, Yuhe
He, Shuangzhi
Wang, Yan
Zhang, Yening
Song, Lili
Wang, Bingmei
Li, Xiumin
author_facet Tang, Lili
Pang, Ying
He, Yi
Shi, Qiuling
Han, Xinkun
Li, Zimeng
Zhou, Chengcheng
Zhou, Yuhe
He, Shuangzhi
Wang, Yan
Zhang, Yening
Song, Lili
Wang, Bingmei
Li, Xiumin
author_sort Tang, Lili
collection PubMed
description INTRODUCTION: An electronic Patient-Reported Outcome (ePRO) platform is needed for implementing evidence-based symptom management in outpatients with advanced cancer. We describe the overall protocol and the methodology for measuring symptom burden, to provide critical parameters needed to implement symptom management on the ePRO platform. METHODS AND ANALYSIS: The study focusses on patients with advanced lung cancer, stomach cancer, oesophagus cancer, liver cancer, colorectal cancer or breast cancer. The primary outcome is the change of symptom burden. MD Anderson Symptom Inventory, and other PRO instruments (Insomnia Severity Index, Hospital Anxiety and Depression Scale, 9-item Patient Health Questionnaire and EuroQol-5 dimensions-5 levels version) were used. The secondary outcomes include feasibility of using ePRO, symptom-related quality of life, reasons for no improvement of symptoms, defining frequency of PRO assessments and cut-points, items for screening and management of comorbidity and satisfaction with ePRO platform in patients and health providers. After initial outpatient visit for baseline assessment, ePRO system will automatically send follow-up notification seven times over 4 weeks to patients. The characteristics and changing trajectory of symptoms of patients will be described. Parameters for using PROs, such as optimal time points for follow-up and cut-off point for alert will be determined. The feasibility of ePRO platform to track the changes of target symptoms in outpatients will be evaluated. ETHICS AND DISSEMINATION: The study protocol and related documents were approved by the Institutional Research Board (IRB) of Peking University Cancer Hospital on 13 February 2019 (2019YJZ07). The results of this study will be disseminated through academic workshops, peer-reviewed publications and conferences. TRIAL REGISTRATION NUMBER: ChiCTR1900023560.
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spelling pubmed-76824472020-11-24 Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol Tang, Lili Pang, Ying He, Yi Shi, Qiuling Han, Xinkun Li, Zimeng Zhou, Chengcheng Zhou, Yuhe He, Shuangzhi Wang, Yan Zhang, Yening Song, Lili Wang, Bingmei Li, Xiumin BMJ Open Palliative Care INTRODUCTION: An electronic Patient-Reported Outcome (ePRO) platform is needed for implementing evidence-based symptom management in outpatients with advanced cancer. We describe the overall protocol and the methodology for measuring symptom burden, to provide critical parameters needed to implement symptom management on the ePRO platform. METHODS AND ANALYSIS: The study focusses on patients with advanced lung cancer, stomach cancer, oesophagus cancer, liver cancer, colorectal cancer or breast cancer. The primary outcome is the change of symptom burden. MD Anderson Symptom Inventory, and other PRO instruments (Insomnia Severity Index, Hospital Anxiety and Depression Scale, 9-item Patient Health Questionnaire and EuroQol-5 dimensions-5 levels version) were used. The secondary outcomes include feasibility of using ePRO, symptom-related quality of life, reasons for no improvement of symptoms, defining frequency of PRO assessments and cut-points, items for screening and management of comorbidity and satisfaction with ePRO platform in patients and health providers. After initial outpatient visit for baseline assessment, ePRO system will automatically send follow-up notification seven times over 4 weeks to patients. The characteristics and changing trajectory of symptoms of patients will be described. Parameters for using PROs, such as optimal time points for follow-up and cut-off point for alert will be determined. The feasibility of ePRO platform to track the changes of target symptoms in outpatients will be evaluated. ETHICS AND DISSEMINATION: The study protocol and related documents were approved by the Institutional Research Board (IRB) of Peking University Cancer Hospital on 13 February 2019 (2019YJZ07). The results of this study will be disseminated through academic workshops, peer-reviewed publications and conferences. TRIAL REGISTRATION NUMBER: ChiCTR1900023560. BMJ Publishing Group 2020-11-20 /pmc/articles/PMC7682447/ /pubmed/33444183 http://dx.doi.org/10.1136/bmjopen-2020-038223 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Palliative Care
Tang, Lili
Pang, Ying
He, Yi
Shi, Qiuling
Han, Xinkun
Li, Zimeng
Zhou, Chengcheng
Zhou, Yuhe
He, Shuangzhi
Wang, Yan
Zhang, Yening
Song, Lili
Wang, Bingmei
Li, Xiumin
Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol
title Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol
title_full Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol
title_fullStr Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol
title_full_unstemmed Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol
title_short Longitudinal study of symptom burden in outpatients with advanced cancers based on electronic Patient-Reported Outcome (ePRO) platform: a single institution, prospective study protocol
title_sort longitudinal study of symptom burden in outpatients with advanced cancers based on electronic patient-reported outcome (epro) platform: a single institution, prospective study protocol
topic Palliative Care
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682447/
https://www.ncbi.nlm.nih.gov/pubmed/33444183
http://dx.doi.org/10.1136/bmjopen-2020-038223
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