Occupational Therapeutic Intervention in children with Duchenne Muscular Dystrophy (DMD): a case study

被引:0
|
作者
Campos Rocha Raboni, Tabita Enila [1 ]
Marino da Silva, Milena Fazzio [2 ]
Pfeifer, Luzia Lara [3 ]
机构
[1] Univ Sao Paulo, FMRP, Terapia Ocupac, Ribeirao Preto, SP, Brazil
[2] Hosp Clin Ribeirao Preto, Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, FMRP, Curso Grad Terapia Ocupac, Ribeirao Preto, SP, Brazil
来源
关键词
Occupational Therapy; Duchenne Muscular Dystrophy; Outpatient Care;
D O I
10.4322/cto.2012.013
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Duchenne muscular dystrophy is a progressive disorder that affects the musculature leading to debility and excessive weakness. This study describes an occupational therapy intervention in a child suffering of Duchenne muscular dystrophy. The intervention sought to prevent the functional inactivity caused by the progressive aggravation process, mainly of the motor coordination, which sometimes causes emotional damage, social isolation, cognitive deficit and family dysfunction, thus aiming to reach a healthy occupational performance. In the initial assessment, the child presented compensatory movements and posture-including roam, difficulty to perform postural changes and poor global motor coordination, but no difficulty in fine-motor coordination as well as in uni/bimanual and prehension functions. Regarding the cognitive aspects, the child showed learning difficulties and was interested only in toys that were inadequate for the age. The main therapeutic goals focused on the performance of occupations related to the activities of daily living (ADLs), playing, education and participation. The treatment occurred from August to November 2007 and from May to July 2009, once a week, 45 minutes in average. AsDuchenne muscular dystrophyis a progressive disorder, some difficulties in walking, standing and keeping the adequate feet positioning intensified, leading to the necessity of using a wheelchair. However, along the treatment, it was possible to notice some adjustment in the playing, motivation in social participation, adequacy to the school environment that enabled progress in this area, as well as more independence in the ADLs, improving the quality of life of the child and the child's family.
引用
收藏
页码:121 / 127
页数:7
相关论文
共 50 条
  • [21] GrowDMD: an international study on transition of youth with Duchenne muscular dystrophy (DMD)
    Friedrich, S.
    Langer, T.
    Reeskau, G.
    Rodger, S.
    Willems, J.
    de Angelis, F.
    Brigladori, B.
    Guastafierro, E.
    Leonardi, M.
    Marcassoli, A.
    Moroni, I.
    Nardocci, N.
    Fournier, A.
    Frei, J.
    Rojas, R. Gutierrez
    De Camargo, O. Kraus
    Pozniak, K.
    Swain, A.
    Gorter, J.
    Osman, H.
    NEUROMUSCULAR DISORDERS, 2024, 43
  • [22] Bone strength in boys with Duchenne muscular dystrophy (DMD): a longitudinal study
    Crabtree, N.
    Ward, K.
    Shaw, N.
    Roper, H.
    Adams, J.
    Mughal, Z.
    NEUROMUSCULAR DISORDERS, 2010, 20 (9-10) : 661 - 661
  • [23] Increased sensitivity to vecuronium (VEC) in children with Duchenne's Muscular Dystrophy (DMD)
    Ririe, DG
    Shapiro, F
    Sethna, NF
    ANESTHESIOLOGY, 1996, 85 (3A) : A1065 - A1065
  • [24] Occupational Therapy and Duchenne Muscular Dystrophy
    Barratt, Sarah J.
    INTERNATIONAL JOURNAL OF THERAPY AND REHABILITATION, 2008, 15 (05): : 220 - 220
  • [25] Duchenne Muscular Dystrophy (DMD) and Vitamin D deficiency
    Tribble, Tyler
    Razdan, Raj
    Upadhyayula, Saila
    Loechner, Karen
    Verma, Sumit
    NEUROLOGY, 2020, 94 (15)
  • [26] EFFECTS OF ALLOPURINOL IN DUCHENNE MUSCULAR-DYSTROPHY (DMD)
    GALLOWAY, J
    JENNINGS, H
    KUTNER, M
    RUDMAN, D
    CLINICAL RESEARCH, 1981, 29 (02): : A429 - A429
  • [27] Bone density in patients with Duchenne muscular dystrophy (DMD)
    Eagle, M
    Rawlings, D
    Straub, V
    Bushby, K
    NEUROMUSCULAR DISORDERS, 2005, 15 (9-10) : 689 - 689
  • [28] Review of Duchenne Muscular Dystrophy (DMD) for the Pediatricians in the Community
    Verma, Sumit
    Anziska, Yaacov
    Cracco, Joan
    CLINICAL PEDIATRICS, 2010, 49 (11) : 1011 - 1017
  • [29] The Process of parental disclosure in Duchenne Muscular dystrophy (DMD)
    Dasani, Pooja
    Clarke, A.
    JOURNAL OF MEDICAL GENETICS, 2011, 48 : S90 - S90
  • [30] DMD Genotypes and Motor Function in Duchenne Muscular Dystrophy
    Muntoni, Francesco
    Signorovitch, James
    Sajeev, Gautam
    Lane, Henry
    Jenkins, Madeline
    Dieye, Ibrahima J.
    Ward, Susan
    McDonald, Craig
    Goemans, Nathalie H.
    Niks, Erik
    Wong, Brenda
    Servais, Laurent
    Straub, Volker
    Guglieri, Michela
    de Groot, Imelda J. M.
    Chesshyre, Mary
    Tian, Cuixia Y.
    Manzur, Adnan
    Mercuri, Eugenio
    Aartsma-Rus, Annemieke
    NEUROLOGY, 2023, 100 (15) : E1540 - E1554