Evidence map›Paper›PMID 37344421›Full record

ArticleInternal medicine (Tokyo, Japan)2024

Caregiver Burden with Duchenne and Becker Muscular Dystrophy in Japan: A Clinical Observation Study.

Masatoshi Ishizaki, Michio Kobayashi, Hiroya Hashimoto, Akinori Nakamura, Yasushi Maeda, Hidetsugu Ueyama, Tsuyoshi Matsumura

Open access · diamondAbstract read
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Masatoshi IshizakiDepartment of Neurology, National Hospital Organization Kumamoto Saishun Medical Center, Japan.
Michio KobayashiDepartment of Neurology, National Hospital Organization Akita National Hospital, Japan.
Hiroya HashimotoClinical Research Management Center, Nagoya City University Hospital, Japan.
Akinori NakamuraDepartment of Neurology, National Hospital Organization Matsumoto Medical Center, Japan.
Yasushi MaedaDepartment of Neurology, National Hospital Organization Kumamoto Saishun Medical Center, Japan.
Hidetsugu UeyamaDepartment of Neurology, National Hospital Organization Kumamoto Saishun Medical Center, Japan.
Tsuyoshi MatsumuraDepartment of Neurology, National Hospital Organization Osaka Toneyama Medical Center, Japan.
Kumamoto Medical Center · JPNational Hospital Organization · JPNagoya City University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Skeletal muscle weakness and cardiomyopathy can be seen in carriers of dystrophinopathy. Therefore, the health management of caregivers of Duchenne/Becker muscular dystrophy (DMD/BMD) patients who are themselves carriers is an important issue. However, few studies have focused on caregivers who have dystrophin mutations. Methods In this cross-sectional study conducted at five hospitals, the daily living, situation medical treatment status, genetic testing, physical assessment, care burden, and quality of life of caregivers of DMD/BMD patients were surveyed. Results The subjects were 36 main caregivers (mean age 55.7±8.4 years old), of whom 52.8% were diagnosed as carriers, 8.3% were noncarriers, and 38.9% were not confirmed. In addition, half of the caregivers were not examined regularly at medical institutions. Of all caregivers, 54.3% had muscle or cardiac symptoms, and 75% had elevated serum creatine kinase levels. The mean Zarit Caregiver Burden Interview (ZBI) total score of current caregivers was 20.9±13.1. The frequency of a ZBI total score ≥25 was significantly higher in caregivers diagnosed as carriers than in caregivers unexamined as carriers (p=0.04). The health-related quality of life score (Short Form 36; SF-36) in caregivers was slightly lower than the Japanese standard scores in the sections of physical functioning, role limitations-physical, bodily pain, and social functioning. Conclusion Some caregivers of DMD/BMD patients can themselves have muscular or cardiac symptoms and a heavy care burden. It is therefore necessary for carrier caregivers, especially women, to undergo regular health checkups and receive appropriate health management.

Indexed as

Muscular Dystrophy, DuchenneCaregiver BurdenCross-Sectional StudiesFemaleHumansJapanMiddle AgedQuality of LifecaregivercarrierDuchenne/Becker muscular dystrophyhealth assessment

Identifiers

PMID37344421
PMCPMC10901721
OpenAlexW4381430698

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.