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dc.contributor.authorTakeuchi, Fumien_US
dc.contributor.authorNakamura, Harumasaen_US
dc.contributor.authorYonemoto, Naohiroen_US
dc.contributor.authorKomaki, Hirofumien_US
dc.contributor.authorRosales, Raymond L.en_US
dc.contributor.authorKornberg, Andrew J.en_US
dc.contributor.authorBretag, Allan H.en_US
dc.contributor.authorDejthevaporn, Charungthaien_US
dc.contributor.authorGoh, Khean Jinen_US
dc.contributor.authorJong, Yuh-Jyhen_US
dc.contributor.authorKim, Dae-Seongen_US
dc.contributor.authorKhadilkar, Satish V.en_US
dc.contributor.authorShen, Dingguoen_US
dc.contributor.authorWong, Kum Thongen_US
dc.contributor.authorChai, Josiahen_US
dc.contributor.authorChan, Sophelia Hoi-Shanen_US
dc.contributor.authorKhan, Saraen_US
dc.contributor.authorOhnmar, Ohnmaren_US
dc.contributor.authorNishino, Ichizoen_US
dc.contributor.authorTakeda, Shin'ichien_US
dc.contributor.authorNonaka, Ikuyaen_US
dc.date.accessioned2020-05-05T00:02:25Z-
dc.date.available2020-05-05T00:02:25Z-
dc.date.issued2020-03-01en_US
dc.identifier.issn0387-7604en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.braindev.2019.12.005en_US
dc.identifier.urihttp://hdl.handle.net/11536/154220-
dc.description.abstractBackground: Several studies on clinical practice for Duchenne muscular dystrophy (DMD) have been conducted in Western countries. However, there have been only a few similar studies in Asia and Oceania. Here, we investigate the steroid therapy-related clinical practice for DMD among the local experts. In 2015, we conducted a DMD expert survey in Asia and Oceania to acquire information regarding patients with DMD and to assess current clinical practice with the cooperation of Asian and Oceanian Myology Centre, a neuromuscular disease research network. Results: We obtained survey responses from 87 out of 148 clinicians (62%) from 13 countries and regions. In China, 1385 DMD patients were followed-up by 5 respondent neurologists, and 84% were between 0 and 9 years of age (15% were 10-19 years, 1% > 19 years). While in Japan, 1032 patients were followed-up by 20 clinicians, and the age distribution was similar between the 3 groups (27% were 0-9 years, 35% were 10-19 years, 38 % were >19 years). Most respondent clinicians (91%) were aware of DMD standard of care recommendations. Daily prednisolone/prednisone administration was used most frequently at initiation (N = 45, 64%). Inconsistent opinion on steroid therapy after loss of ambulation and medication for bone protection was observed. Conclusions: Rare disease research infrastructures have been underdeveloped in many of Asian and Oceanian countries. In this situation, our results show the snapshots of current medical situation and clinical practice in DMD. For further epidemiological studies, expansion of DMD registries is necessary. (C) 2020 The Authors. Published by Elsevier B.V. on behalf of The Japanese Society of Child Neurology.en_US
dc.language.isoen_USen_US
dc.subjectDuchenne muscular dystrophyen_US
dc.subjectSteroid therapyen_US
dc.subjectClinical practiceen_US
dc.subjectEpidemiologyen_US
dc.subjectCare recommendationen_US
dc.subjectAsian and Oceanian Myology Centeren_US
dc.titleClinical practice with steroid therapy for Duchenne muscular dystrophy: An expert survey in Asia and Oceaniaen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.braindev.2019.12.005en_US
dc.identifier.journalBRAIN & DEVELOPMENTen_US
dc.citation.volume42en_US
dc.citation.issue3en_US
dc.citation.spage277en_US
dc.citation.epage288en_US
dc.contributor.department生物科技學院zh_TW
dc.contributor.departmentCollege of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000521520500006en_US
dc.citation.woscount0en_US
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