Vibration Therapy Tolerated in Children With Duchenne Muscular Dystrophy: A Pilot Study

被引:14
|
作者
Myers, Kenneth A. [1 ]
Ramage, Barbara [2 ]
Khan, Aneal [3 ]
Mah, Jean K. [1 ]
机构
[1] Univ Calgary, Alberta Childrens Hosp, Dept Pediat, Neurol Sect, Calgary, AB, Canada
[2] Univ Calgary, Alberta Childrens Hosp, Dept Pediat, Riddell Movement Assessment Ctr, Calgary, AB, Canada
[3] Univ Calgary, Alberta Childrens Hosp, Dept Med Genet & Pediat, Calgary, AB, Canada
关键词
Duchenne muscular dystrophy; side-alternating vibration therapy; whole-body vibration therapy; rehabilitation; safety; WHOLE-BODY VIBRATION; FUNCTIONAL MOBILITY; MUSCLE STRENGTH; PERFORMANCE; BONE;
D O I
10.1016/j.pediatrneurol.2014.03.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Duchenne muscular dystrophy is an X-linked recessive muscular dystrophy. Clinical management primarily involves rehabilitation strategies aimed at preserving functional mobility as long as possible. Side-alternating vibration therapy is a rehabilitation intervention that has shown promise in a number of different neuromuscular disorders, and has the potential to preserve strength, functional mobility, and bone mass. There has been little research regarding the tolerance to side-alternating vibration therapy in muscle diseases such as Duchenne muscular dystrophy. METHODS: Four patients were recruited for a pilot study assessing the safety and tolerance of side-alternating vibration therapy in individuals with Duchenne muscular dystrophy. All patients participated in a 4-week training period involving side-alternating vibration therapy sessions three times per week. Serum creatine kinase was measured, and adverse effects reviewed at each session with functional mobility assessed before and after the training period. RESULTS: All patients tolerated the training protocol well, and there were no major changes in functional mobility. One patient had a transient increase in creatine kinase during the study; however, levels of this enzyme were stable overall when comparing the pretraining and posttraining values. Some patients reported subjective improvement during the training period. CONCLUSIONS: Side-alternating vibration therapy is well tolerated in children with Duchenne muscular dystrophy and may have potential to improve or maintain functional mobility and strength in these patients.
引用
收藏
页码:126 / 129
页数:4
相关论文
共 50 条
  • [1] Whole-body vibration training in children with Duchenne muscular dystrophy and spinal muscular atrophy
    Vry, Julia
    Schubert, Isabel J.
    Semler, Oliver
    Haug, Verena
    Schoenau, Eckhard
    Kirschner, Janbernd
    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2014, 18 (02) : 140 - 149
  • [2] Disabilities in children with Duchenne muscular dystrophy: A profile
    Nair, KPS
    Vasanth, A
    Gourie-Devi, M
    Taly, AB
    Rao, S
    Gayathri, N
    Murali, T
    JOURNAL OF REHABILITATION MEDICINE, 2001, 33 (04) : 147 - 149
  • [3] A pilot study of newborn screening for Duchenne muscular dystrophy in Guangzhou
    Jia, Xuefang
    Jiang, Xiang
    Huang, Yonglan
    HELIYON, 2022, 8 (10)
  • [4] Gene therapy for Duchenne muscular dystrophy
    Suzuki, Naoki
    Miyagoe-Suzuki, Yuko
    Takeda, Shin'ichi
    FUTURE NEUROLOGY, 2007, 2 (01) : 87 - 96
  • [5] Gene therapy in Duchenne muscular dystrophy
    Inui, K
    Okada, S
    Dickson, G
    BRAIN & DEVELOPMENT, 1996, 18 (05) : 357 - 361
  • [6] Gene therapy for Duchenne muscular dystrophy
    Ramos, Julian
    Chamberlain, Jeffrey S.
    EXPERT OPINION ON ORPHAN DRUGS, 2015, 3 (11): : 1255 - 1266
  • [7] Gene therapy for Duchenne muscular dystrophy
    Verhaart, Ingrid E. C.
    Aartsma-Rus, Annemieke
    CURRENT OPINION IN NEUROLOGY, 2012, 25 (05) : 588 - 596
  • [8] Fighting Against Disuse of the Masticatory System in Duchenne Muscular Dystrophy: A Pilot Study Using Chewing Gum
    van Bruggen, H. Willemijn
    van den Engel-Hoek, Lenie
    Steenks, Michel H.
    van der Bilt, Andries
    Bronkhorst, Ewald M.
    Creugers, Nico H. J.
    de Groot, Imelda J. M.
    Kalaykova, Stanimira I.
    JOURNAL OF CHILD NEUROLOGY, 2015, 30 (12) : 1625 - 1632
  • [9] Prophylactic oral bisphosphonate therapy in duchenne muscular dystrophy
    Srinivasan, Ramesh
    Rawlings, David
    Wood, Claire L.
    Cheetham, Tim
    Moreno, Aura Cecilia Jimenez
    Mayhew, Anna
    Eagle, Michelle
    Guglieri, Michela
    Straub, Volker
    Owen, Catherine
    Bushby, Kate
    Sarkozy, Anna
    MUSCLE & NERVE, 2016, 54 (01) : 79 - 85
  • [10] Pilot study of a virtual weight management program for Duchenne muscular dystrophy
    Billich, Natassja
    Bray, Paula
    Truby, Helen
    Evans, Maureen
    Carroll, Kate
    de Valle, Katy
    Adams, Justine
    Kennedy, Rachel A.
    Villano, Daniella
    Kornberg, Andrew J.
    Yiu, Eppie M.
    Ryan, Monique M.
    Davidson, Zoe E.
    MUSCLE & NERVE, 2024, 69 (04) : 459 - 466