Evidence map›Paper›PMID 40584434›Full record

ArticleNeuro-oncology advances

Health-related quality of life and psychological distress in patients with brain tumors and their families: A cross-sectional web survey.

Iori Sato, Mari Ikeda, Akemi Tsumura, Yoshitaka Narita

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Iori SatoDepartment of Family Nursing, Division of Health Sciences and Nursing, Graduate School of Medicine, The University of Tokyo, Japan.
Mari IkedaDepartment of Family Nursing, Division of Health Sciences and Nursing, Graduate School of Medicine, The University of Tokyo, Japan.
Akemi TsumuraYokohama Children's Hospice Project, Kanagawa, Japan.
Yoshitaka NaritaDepartment of Neurosurgery and Neuro-oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4303-6006

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The diagnosis and treatment of brain tumors significantly impact not only patients but also their families. To develop better supportive care, it is essential to understand their quality of life (QOL) in detail. Methods: The Supportive Care for Brain Tumor Patients study group conducted a web survey targeting individuals aged 18 and above. Participants were recruited from a Japanese cohort and included patients and family members who responded to both the EQ-5D-5L (health-related QOL [HRQL]) and K6 (psychological distress) scales. Scores were compared with those of the general population, and multivariable regression analyses were performed. Results: A total of 136 patients and 103 family members were analyzed. Patients' HRQL was lower than that of the general population. Family members' psychological distress was higher than that of the general population. Factors associated with these quality-of-life indicators differed between patients and family members: decreased HRQL in patients was associated with financial hardship, being a homemaker, longer duration since diagnosis, and under treatment/relapse, while psychological distress in family members was associated with financial hardship and longer commuting time for hospital visits. Conclusions: The diagnosis and treatment of brain tumors significantly impact QOL for both patients and their families. In particular, support for the psychological well-being of family members is crucial, with emphasis on the importance of addressing lifestyle and caregiving needs.

Indexed as

brain tumorfamilygliomahealth-related quality of lifepsychological distress

Identifiers

PMID40584434
PMCPMC12202142

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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.