Literature DB >> 33387291

Feasibility of health-related quality of life (HRQoL) assessment for cancer patients using electronic patient-reported outcome (ePRO) in daily clinical practice.

Guillaume Mouillet1,2,3, Antoine Falcoz4,5, Joëlle Fritzsch4,5, Hamadi Almotlak6, Pascale Jacoulet7, Xavier Pivot8, Cristian Villanueva9, Laura Mansi6,5, Stefano Kim6,5, Elsa Curtit6,5, Nathalie Meneveau6, Olivier Adotevi6,5, Marine Jary6,5, Guillaume Eberst5,7, Angelique Vienot6,5, Fabien Calcagno6, Astrid Pozet4,5, Oumelkheir Djoumakh4,5, Christophe Borg6,5, Virginie Westeel4,5,7, Amélie Anota4,5,10, Sophie Paget-Bailly4,5.   

Abstract

INTRODUCTION: Routine Electronic Monitoring of Health-Related Quality of Life (HRQoL) (REMOQOL) in clinical care with real-time feedback to physicians could help to enhance patient-centered care. We evaluated the feasibility of REMOQOL in the French context in the QOLIBRY study. The primary objective was to assess the patients' compliance with REMOQOL.
METHODS: The QOLIBRY study was a single-center, prospective study conducted in the University Hospital of Besançon (France). Eligible patients were those treated with systemic therapies for breast, lung or colorectal cancer at any stage. Patients were invited to complete the EORTC QLQ-C30 questionnaire and cancer-site-specific modules before each visit on tablets and/or computers in the hospital or at home. During the consultation, physicians had real-time access to visual summaries of HRQoL scores. Compliance was assessed as adequate if at least 66% of HRQoL assessments were completed during the 4 months of follow-up.
RESULTS: Between March 2016 and October 2018, 177 patients were included in the QOLIBRY study. Median age was 64 years (IQR 54-71). The proportion of patients with an adequate compliance rate was 95.5% (n = 63) in the breast cancer cohort, 98.2% (n = 55) in the colorectal cancer cohort, and 90.9% (n = 50) in the lung cancer cohort. The physicians checked the HRQoL results in 73.1% of visits and prescribed supportive care and adapted patient management in 8.3% and 5.2% of visits, respectively. CONCLUSION & PERSPECTIVES: The results of QOLIBRY study suggest that REMOQOL is feasible in the French context. However, information about HRQoL monitoring, training of the physicians in the use of the software, and recommendations for using HRQoL results to guide care are essential and must be improved.

Entities:  

Keywords:  Clinical practice; Electronic questionnaire; Health-related quality of life; Oncology; Patient-centered care; Patient-reported outcome

Year:  2021        PMID: 33387291     DOI: 10.1007/s11136-020-02721-0

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  31 in total

1.  Randomized Trial Comparing a Web-Mediated Follow-up With Routine Surveillance in Lung Cancer Patients.

Authors:  Fabrice Denis; Claire Lethrosne; Nicolas Pourel; Olivier Molinier; Yoann Pointreau; Julien Domont; Hugues Bourgeois; Hélène Senellart; Pierre Trémolières; Thibaut Lizée; Jaafar Bennouna; Thierry Urban; Claude El Khouri; Alexandre Charron; Anne-Lise Septans; Magali Balavoine; Sébastien Landry; Philippe Solal-Céligny; Christophe Letellier
Journal:  J Natl Cancer Inst       Date:  2017-09-01       Impact factor: 13.506

Review 2.  Patient-reported outcome use in oncology: a systematic review of the impact on patient-clinician communication.

Authors:  L Y Yang; D S Manhas; A F Howard; R A Olson
Journal:  Support Care Cancer       Date:  2017-08-28       Impact factor: 3.603

Review 3.  Analysing data from patient-reported outcome and quality of life endpoints for cancer clinical trials: a start in setting international standards.

Authors:  Andrew Bottomley; Madeline Pe; Jeff Sloan; Ethan Basch; Franck Bonnetain; Melanie Calvert; Alicyn Campbell; Charles Cleeland; Kim Cocks; Laurence Collette; Amylou C Dueck; Nancy Devlin; Hans-Henning Flechtner; Carolyn Gotay; Eva Greimel; Ingolf Griebsch; Mogens Groenvold; Jean-Francois Hamel; Madeleine King; Paul G Kluetz; Michael Koller; Daniel C Malone; Francesca Martinelli; Sandra A Mitchell; Carol M Moinpour; Jammbe Musoro; Daniel O'Connor; Kathy Oliver; Elisabeth Piault-Louis; Martine Piccart; Francisco L Pimentel; Chantal Quinten; Jaap C Reijneveld; Christoph Schürmann; Ashley Wilder Smith; Katherine M Soltys; Martin J B Taphoorn; Galina Velikova; Corneel Coens
Journal:  Lancet Oncol       Date:  2016-10-18       Impact factor: 41.316

Review 4.  Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors.

Authors:  D Howell; S Molloy; K Wilkinson; E Green; K Orchard; K Wang; J Liberty
Journal:  Ann Oncol       Date:  2015-04-17       Impact factor: 32.976

Review 5.  Improving patient outcomes through the routine use of patient-reported data in cancer clinics: future directions.

Authors:  T Luckett; P N Butow; M T King
Journal:  Psychooncology       Date:  2009-11       Impact factor: 3.894

6.  Symptom Monitoring With Patient-Reported Outcomes During Routine Cancer Treatment: A Randomized Controlled Trial.

Authors:  Ethan Basch; Allison M Deal; Mark G Kris; Howard I Scher; Clifford A Hudis; Paul Sabbatini; Lauren Rogak; Antonia V Bennett; Amylou C Dueck; Thomas M Atkinson; Joanne F Chou; Dorothy Dulko; Laura Sit; Allison Barz; Paul Novotny; Michael Fruscione; Jeff A Sloan; Deborah Schrag
Journal:  J Clin Oncol       Date:  2015-12-07       Impact factor: 44.544

7.  Electronic self-report assessment for cancer and self-care support: results of a multicenter randomized trial.

Authors:  Donna L Berry; Fangxin Hong; Barbara Halpenny; Ann H Partridge; Jesse R Fann; Seth Wolpin; William B Lober; Nigel E Bush; Upendra Parvathaneni; Anthony L Back; Dagmar Amtmann; Rosemary Ford
Journal:  J Clin Oncol       Date:  2013-12-16       Impact factor: 44.544

Review 8.  Exploring the implementation of patient-reported outcome measures in cancer care: need for more real-world evidence results in the peer reviewed literature.

Authors:  Milena Anatchkova; Sarah M Donelson; Anne M Skalicky; Colleen A McHorney; Dayo Jagun; Jennifer Whiteley
Journal:  J Patient Rep Outcomes       Date:  2018-12-27

Review 9.  A systematic review of the impact of routine collection of patient reported outcome measures on patients, providers and health organisations in an oncologic setting.

Authors:  Jack Chen; Lixin Ou; Stephanie J Hollis
Journal:  BMC Health Serv Res       Date:  2013-06-11       Impact factor: 2.655

Review 10.  The use and impact of quality of life assessment tools in clinical care settings for cancer patients, with a particular emphasis on brain cancer: insights from a systematic review and stakeholder consultations.

Authors:  Sarah King; Josephine Exley; Sarah Parks; Sarah Ball; Teresa Bienkowska-Gibbs; Calum MacLure; Emma Harte; Katherine Stewart; Jody Larkin; Andrew Bottomley; Sonja Marjanovic
Journal:  Qual Life Res       Date:  2016-04-02       Impact factor: 4.147

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  1 in total

1.  COVID-19 Induced Environments, Health-Related Quality of Life Outcomes and Problematic Behaviors: Evidence from Children with Syndromic Autism Spectrum Disorders.

Authors:  Corneliu Bolbocean; Kayla B Rhidenour; Maria McCormack; Bernhard Suter; J Lloyd Holder
Journal:  J Autism Dev Disord       Date:  2022-06-07
  1 in total

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