TY - JOUR
T1 - Clinical practice with steroid therapy for Duchenne muscular dystrophy
T2 - An expert survey in Asia and Oceania
AU - Takeuchi, Fumi
AU - Nakamura, Harumasa
AU - Yonemoto, Naohiro
AU - Komaki, Hirofumi
AU - Rosales, Raymond L.
AU - Kornberg, Andrew J.
AU - Bretag, Allan H.
AU - Dejthevaporn, Charungthai
AU - Goh, Khean Jin
AU - Jong, Yuh Jyh
AU - Kim, Dae Seong
AU - Khadilkar, Satish V.
AU - Shen, Dingguo
AU - Wong, Kum Thong
AU - Chai, Josiah
AU - Chan, Sophelia Hoi Shan
AU - Khan, Sara
AU - Ohnmar, Ohnmar
AU - Nishino, Ichizo
AU - Takeda, Shin'ichi
AU - Nonaka, Ikuya
N1 - Publisher Copyright:
© 2020 The Japanese Society of Child Neurology
PY - 2020/3
Y1 - 2020/3
N2 - Background: 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.
AB - Background: 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.
KW - Asian and Oceanian Myology Center
KW - Care recommendation
KW - Clinical practice
KW - Duchenne muscular dystrophy
KW - Epidemiology
KW - Steroid therapy
UR - http://www.scopus.com/inward/record.url?scp=85078191407&partnerID=8YFLogxK
U2 - 10.1016/j.braindev.2019.12.005
DO - 10.1016/j.braindev.2019.12.005
M3 - Article
C2 - 31980267
AN - SCOPUS:85078191407
SN - 0387-7604
VL - 42
SP - 277
EP - 288
JO - Brain and Development
JF - Brain and Development
IS - 3
ER -