Evidence map›Paper›PMID 38243309›Full record

ArticleHealth and quality of life outcomes2024

Perceptions regarding the concept and definition of patient-reported outcomes among healthcare stakeholders in Japan with relation to quality of life: a cross-sectional study.

Takako Kaneyasu, Shinya Saito, Kikuko Miyazaki, Yoshimi Suzukamo, Mariko Naito, Takashi Kawaguchi, Takako Eguchi Nakajima, Takuhiro Yamaguchi, Kojiro Shimozuma

Abstract read
In one paragraph

Article in Health and quality of life outcomes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Takako KaneyasuDepartment of Biomedical Sciences, Ritsumeikan University, Shiga, Japan. kaneyasu@fc.ritsumei.ac.jp.
Shinya SaitoOkayama University Graduate School of Health Sciences, Okayama, Japan.
Kikuko MiyazakiDepartment of Health Informatics, Graduate School of Medicine & School of Public Health, Kyoto University, Kyoto, Japan.
Yoshimi SuzukamoDepartment of Physical Medicine and Rehabilitation, Tohoku University Graduate School of Medicine, Miyagi, Japan.
Mariko NaitoDepartment of Oral Epidemiology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Takashi KawaguchiSchool of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
Takako Eguchi NakajimaDepartment of Early Clinical Development Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takuhiro YamaguchiDivision of Biostatistics, Tohoku University Graduate School of Medicine, Tohoku University, Miyagi, Japan.
Kojiro ShimozumaDepartment of Biomedical Sciences, Ritsumeikan University, Shiga, Japan.

Funding

Ministry of Health, Labour and Welfare JPMH20AC1003
6 · The paper itself

Abstract

Patient-reported outcomes (PROs) are frequently used in a variety of settings, including clinical trials and clinical practice. The definition of PRO and quality of life (QOL) and their relationship have been concluded through discussions among experts that has been the premise of PRO guidelines are not clearly stated in the guidelines. Therefore, the definition of PRO, especially in relation to QOL, is sometimes explained simply, as "PRO includes QOL," but this complicated matters. This study investigated the perceptions of PRO among various stakeholders (including patients and their families, the industry, clinicians, regulatory or health technology assessment personnel, and academic researchers) in Japan to clarify its definitions and that of QOL, including their relationship.We conducted a two-step survey: a qualitative interview survey and a web-based survey to ensure the validity of the survey. During the interviews, eight stakeholders described their perceptions and thoughts on PRO and its relationship to QOL, and their experience of using PRO. Overall 253 clinicians, 249 company employees, and 494 patients participated in the web survey to confirm how the findings of the interview survey supported the results.In the interview survey, patient advocates described various perspectives of PRO and QOL, including unexpected dynamic relationships, while the most other stakeholders explained PRO and QOL with the language used in the guidelines, but their responses were split. The web-based survey revealed that all stakeholders had a lower awareness of PRO than QOL. The most common perception of PRO, especially in the relationship to QOL, was "they did not fully overlap." Although there were differences in perceptions of the relationship between PRO and QOL among clinicians, company employees, and patients, all perceived PRO as a tool to facilitate communication in clinical practice.The present results are inconsistent with the simplified explanation of PRO, but consistent with the original PRO guideline definitions, which also considered the role of PRO in clinical practice. To make PRO a more potent tool, all stakeholders using PRO should confirm its definition and how it differs from QOL, have a unified recognition in each PRO use, and avoid miscommunication.

Indexed as

Patient Reported Outcome MeasuresQuality of LifeCross-Sectional StudiesDelivery of Health CareHumansJapan

Identifiers

PMID38243309
PMCPMC10797787

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.