Seated Outcome Measures in Children With Duchenne Muscular Dystrophy

被引:0
|
作者
Kern, Rebecca [1 ,2 ]
Carvell, Kimberly [1 ]
Gupta, Apeksha [3 ]
Verma, Sumit [1 ,4 ]
机构
[1] Childrens Healthcare Atlanta, Dept Rehabil & Neurosci, Atlanta, GA USA
[2] Pasco Cty Sch, Student Support Programs & Serv, Land O Lakes, FL USA
[3] Nicklaus Childrens Hosp, Personalized Med Initiat & Hlth Outcomes, Miami, FL USA
[4] Emory Univ, Sch Med, Dept Pediat & Neurol, Atlanta, GA USA
关键词
Duchenne muscular dystrophy; hand-held dynamometry; Pediatric Evaluation of Disability Inventory; seated reach distance; seated trunk strength; sitting balance; NATURAL-HISTORY; MUSCLE WEAKNESS; CLINICAL-TRIAL; RELIABILITY; VALIDITY; TRUNK;
D O I
10.1097/PEP.0000000000000916
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: Quantifiable motor strength measures to assess disease severity throughout the continuum of Duchenne muscular dystrophy (DMD) are needed. To study the feasibility of seated trunk strength using hand-held dynamometry (HHD) and caregiver-reported subjective functional independence measures in boys with DMD. Methods: Prospective, cross-sectional, observational study of 18 participants with DMD enrolled from pediatric muscular dystrophy clinic during routine clinical assessment. Hand-held dynamometry, seated reach distance test and Pediatric Evaluation of Disability Inventory (PEDI) were administered. Results: All study participants regardless of the walking status were able to complete the seated function tests demonstrating feasibility. The age of the participants correlated negatively with PEDI mobility and positively with HHD extension scores. The seated measures did not statistically correlate with PEDI mobility scores. Conclusions: Seated motor strength measures and PEDI mobility scores are feasible. The PEDI mobility and HHD extension scores correlate with age. Study limitations included single-center experience and cross-sectional data. Video abstract link: https://www.dropbox.com/s/s4r0k7o6s0tfbkb/PT-Seated-Measures-And-DMD-2022.mp4?dl=0
引用
收藏
页码:375 / 380
页数:6
相关论文
共 50 条
  • [21] Electrocardiographic features of children with Duchenne muscular dystrophy
    Tang, Liting
    Shao, Shuran
    Wang, Chuan
    ORPHANET JOURNAL OF RARE DISEASES, 2022, 17 (01)
  • [22] Spinal management of Duchenne muscular dystrophy in children
    D'Astous, Jacques
    CURRENT ORTHOPAEDIC PRACTICE, 2012, 23 (05): : 448 - 452
  • [23] Health-Related Quality of Life in Children and Adolescents With Duchenne Muscular Dystrophy
    Uzark, Karen
    King, Eileen
    Cripe, Linda
    Spicer, Robert
    Sage, Jackie
    Kinnett, Kathleen
    Wong, Brenda
    Pratt, Jesse
    Varni, James W.
    PEDIATRICS, 2012, 130 (06) : E1559 - E1566
  • [24] Reliability and Validity of the Trunk Control Measurement Scale in Children With Duchenne Muscular Dystrophy
    Bulut, Numan
    Aydin Yagcioglu, Gullu
    Yardimci-Lokmanoglu, Bilge Nur
    Alemdaroglu-Gurbuz, Ipek
    Yilmaz, Oznur
    Karaduman, Ayse
    PERCEPTUAL AND MOTOR SKILLS, 2024, 131 (06) : 2167 - 2181
  • [25] Thoracic cirtometry in children with Duchenne muscular dystrophy - expansion of the method
    Garcia Junior, Agenor
    Caromano, Fatima A.
    Contesini, Adriana M.
    Escorcio, Renata
    Fernandes, Lilian A. Y.
    Joao, Silvia M. A.
    BRAZILIAN JOURNAL OF PHYSICAL THERAPY, 2013, 17 (01) : 1 - 8
  • [26] Safety and clinical outcome of tamoxifen in Duchenne muscular dystrophy
    Tsabari, Reuven
    Simchovitz, Elana
    Lavi, Eran
    Eliav, Osnat
    Avrahami, Ran
    Ben-Sasson, Shmuel
    Dor, Talya
    NEUROMUSCULAR DISORDERS, 2021, 31 (09) : 803 - 813
  • [27] Outcome Measures in Facioscapulohumeral Muscular Dystrophy Clinical Trials
    Ghasemi, Mehdi
    Emerson, Charles P., Jr.
    Hayward, Lawrence J.
    CELLS, 2022, 11 (04)
  • [28] Duchenne muscular dystrophy
    Yiu, Eppie M.
    Kornberg, Andrew J.
    NEUROLOGY INDIA, 2008, 56 (03) : 236 - 247
  • [29] Uncertainty, hope, and coping efficacy among mothers of children with Duchenne/Becker muscular dystrophy
    Bell, Megan
    Biesecker, Barbara B.
    Bodurtha, Joann
    Peay, Holly L.
    CLINICAL GENETICS, 2019, 95 (06) : 677 - 683
  • [30] The association between trunk control and upper limb functions of children with Duchenne muscular dystrophy
    Bulut, Numan
    Alemdaroglu-Gurbuz, Ipek
    Topaloglu, Haluk
    Yilmaz, Oznur
    Karaduman, Ayse
    PHYSIOTHERAPY THEORY AND PRACTICE, 2022, 38 (01) : 46 - 54