Social difficulties and costs/burden of adult Duchenne muscular dystrophy in Japan: A questionnaire survey based on the Japanese Registry of Muscular Dystrophy (Remudy)

Author:

Mori-Yoshimura Madoka1ORCID,Ishigaki Keiko2,Shimizu-Motohashi Yuko3,Ishihara Naoko4,Unuma Atushi1,Yoshida Sumiko5,Nakamura Harumasa6

Affiliation:

1. Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry

2. Department of Pediatrics, Tokyo Women's Medical Collage

3. Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry

4. Medical Genome Center, National Center of Neurology and Psychiatry

5. Department of Psychiatry, National Center Hospital, National Center of Neurology and Psychiatry

6. Department of Clinical Research Support, National Center Hospital, National Center of Neurology and Psychiatry

Abstract

Abstract Background Little is known about the social difficulties, economic burden, and health care needs of adult Duchenne muscular dystrophy (DMD) patients in Japan, as well as the financial and physical stress experienced by their caregivers. This study aimed to clarify the social circumstances surrounding adult DMD patients and assess the degree of involvement of family members in their care and the associated economic burden of the disorder in Japan. Methods Adult DMD patients were identified through the Registry of Muscular Dystrophy (Remudy) in Japan and invited to complete a questionnaire together with a caregiver. Data on health care use, quality of life, work status, informal care, and household expenses were collected to estimate the costs associated with DMD from social and caregiver household perspectives. Results In total, 234 (63.7%) of 367 adult DMD patients (mean age, 27.4 ± 6.0; range, 20–48 years) completed the questionnaire. Of these, 38 (21%) had developmental disorders (mental retardation, autism, and learning disorders), 57 (33%) experienced bullying in school, and 44 (77%) indicated the reason for bullying to be their physical handicap. Employment histories were noted by 72 (31%), although 23 (10%) lost their jobs mainly due to physical difficulties. Of the 234 patients, 164 (74%) lived with their relatives, and 78% of care time was supplied by family members, in particular, their mothers. The mean rate of care work provided by family members was 81%. Household income of families with an adult DMD patient was lower, whereas the rate of living with parent(s) and grandparent(s) was higher, in comparison with the general Japanese population. Conclusions Adult DMD patients in Japan experience many social difficulties from childhood up to adulthood. As adults, many DMD patients experience bullying and workplace difficulties. Families were found to provide most of the care and financial support for DMD patients. Our results suggest the need to improve public patient care systems, including financial support, to address the physical and economic burdens of care for adult DMD patients in Japan.

Publisher

Research Square Platform LLC

Reference16 articles.

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2. Dystrophin and mutations: one gene, several proteins, multiple phenotypes;Muntoni F;Lancet Neurol,2003

3. The muscular dystrophies;Emery AE;Lancet,2002

4. A longitudinal cause-of-death analysis of patients with Duchenne muscular dystrophy;Matsumura T;Rinsyo Shinkeigaku,2011

5. 2021 Annual income of household. Ministry of Health, Labor and Welfare (in Japanese) https://www.mhlw.go.jp/toukei/saikin/hw/k-tyosa/k-tyosa21/dl/03.pdf. Accessed 30th January 2023

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