Evidence map›Paper›PMID 41883814›Full record

ArticleTherapeutic advances in rare disease

Reliability assessment using the test-retest method and minimal important changes in the Adult Fabry Disease Quality of Life Scale.

Yuta Koto, Masami Tanaka, Mitsuyo Ishiura, HyeSook Kim, Atsushi Ohashi, Nozomi Hadano, Aya Narita, Norio Sakai

Abstract read
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Article in Therapeutic advances in rare disease. 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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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

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yuta KotoFaculty of Nursing, Kansai Medical University, 2-2-2 Shinmachi, Hirakata, Osaka 573-1004, Japan.ORCID https://orcid.org/0000-0003-4314-4955
Masami TanakaFaculty of Nursing, Kansai Medical University, Hirakata City, Osaka, Japan.ORCID https://orcid.org/0009-0002-0211-1049
Mitsuyo IshiuraFaculty of Nursing, Kansai Medical University, Hirakata City, Osaka, Japan.
HyeSook KimFaculty of Nursing, Kansai Medical University, Hirakata City, Osaka, Japan.
Atsushi OhashiFaculty of Nursing, Kansai Medical University, Hirakata City, Osaka, Japan.
Nozomi HadanoDepartment of Nursing, Faculty of Nursing, Shitennoji University, Habikino City, Osaka, Japan.ORCID https://orcid.org/0000-0002-8044-4757
Aya NaritaCenter for Promoting the Treatment of Intractable Diseases, ISEIKAI International General Hospital, Osaka City, Osaka, Japan.
Norio SakaiCenter for Promoting the Treatment of Intractable Diseases, ISEIKAI International General Hospital, Osaka City, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Fabry disease is rare and multisystemic, necessitating a disease-specific quality of life scale to assess changes in quality of life. We developed the Adult Fabry Disease Quality of Life scale to measure the quality of life of adult patients with Fabry disease. Objectives: To confirm the reliability of the Adult Fabry Disease Quality of Life scale using the test-retest method and calculate the minimal important change. Design: This study was based on two questionnaire surveys conducted at approximately 2-week intervals in November and December 2024 in Japan. Methods: Twenty-eight participants completed questionnaires consisting of background information, the Adult Fabry Disease Quality of Life scale, and the Short Form-8. In the second survey, an anchor question with a 7-point Likert scale was added to assess changes in general health. The intraclass correlation coefficient for reliability and Cronbach's alpha coefficient for internal consistency were calculated. For minimal important changes, the average value of the smallest change group for the anchor question was calculated. Results: The intraclass correlation coefficients for each factor and the total score on the Adult Fabry Disease Quality of Life scale were 0.892-0.946. Cronbach's alpha coefficient was 0.948 for the first survey and 0.956 for the second. In response to the anchor question, three participants (13.0%) felt a little worse, and three (13.0%) felt a little better. Those who felt a little worse and those who felt a little better showed improvements in quality of life of 3.7 and 5.3 points, respectively. Conclusion: The Adult Fabry Disease Quality of Life scale is highly reproducible at 2-week intervals. Defining the minimum important change was not possible, which is important when used as an outcome. Future studies should establish it using the anchor method. Trial Registration: This prospective study was registered with the UMIN-CTR on September 1, 2024 (No. UMIN000055144).

Indexed as

Fabry diseaselysosomal storage diseasesminimal clinically important differencesquality of life

Identifiers

PMID41883814
PMCPMC13009963

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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.