Lung volume recruitment in patients with Duchenne Muscular Dystrophy in the early non-ambulatory stage

被引:0
作者
Alvarez, Wendy [1 ]
Montero, Sebastian [1 ]
Huerta, Antonio [2 ,3 ]
Moraga, Arlette [1 ]
Saavedra, Cristian [1 ]
Solis, Fresia [1 ]
Prado, Francisco [2 ,3 ,4 ]
机构
[1] Inst Teleton Santiago, Santiago, Chile
[2] Hosp Clin San Borja Arriaran, Serv Pediat, Unidad Hospitalizac Domiciliaria NANEAS, Santiago, Chile
[3] Grp Iberoamer Cuidados Resp Enfermedades Neuromusc, Santiago, Chile
[4] Univ Chile, Dept Pediat & Cirugia, Campus Ctr, Santiago, Chile
来源
ANDES PEDIATRICA | 2025年 / 96卷 / 01期
关键词
Duchenne Muscular Dystrophy; Neuromuscular Disease; Vital Capacity; Cough; Respiratory Muscles; Rehabilitation Center; QUALITY-OF-LIFE; VITAL CAPACITY; INSUFFLATION CAPACITY; RESPIRATORY-FUNCTION; AIR STACKING; VENTILATION; DISORDERS; DIAGNOSIS; HEALTHY;
D O I
10.32641/andespediatr.v96i1.5190
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Ventilatory and cough insufficiency are the main causes of morbidity and mortality in patients with Duchenne muscular dystrophy (DMD). Lung volume recruitment (LVR) might decrease the decline in vital capacity (VC). Objective: To determine the changes produced by respiratory training performed at home with LVR techniques and manually assisted cough on VC, maximum insufflation capacity (MIC), and peak cough flow (PCF) in adolescents with DMD in the early non-ambulatory stage. Patients and Method: Quasi-experimental study with repeated measurements every three months. 16 adolescents with DMD close to the CV plateau and cough insufficiency were evaluated and trained daily in LVR and assisted cough, with follow-up for 12 months, assessing respiratory function, quality of life, and caregiver overload. Results: Eleven users (69%), aged 12.7 +/- 2.8 years, completed the follow-up. Supine position VC and PCF + compression increased significantly (p = 0.047; p = 0.012, respectively). Seated VC and MIC tended to improve by 11.2% and 21.6%, respectively. Quality of life and caregiver overload did not present significant changes. Conclusion: In adolescents with DMD in the early non-ambulatory stage, significant improvements were observed in VC and cough capacity. This provides an intervention of easy implementation, capable of preventing the expected respiratory functional decline.
引用
收藏
页码:23 / 32
页数:10
相关论文
共 50 条
  • [31] Emergency department care of patients with Duchenne muscular dystrophy
    Woods, William A.
    Harmon, William G.
    Webb, Lauren W.
    Robinson, Grant G.
    McCulloch, Michael A.
    AMERICAN JOURNAL OF EMERGENCY MEDICINE, 2022, 60 : 101 - 105
  • [32] Cardiac assessment of patients with late stage Duchenne muscular dystrophy
    E. A. P. van Bockel
    J. S. Lind
    J. G. Zijlstra
    P. J. Wijkstra
    P. M. Meijer
    M. P. van den Berg
    R. H. J. A. Slart
    L. P. H. J. Aarts
    J. E. Tulleken
    Netherlands Heart Journal, 2009, 17 : 232 - 237
  • [33] Impact of Noninvasive Ventilation on Lung Volumes and Maximum Respiratory Pressures in Duchenne Muscular Dystrophy
    Santos, Dante Brasil
    Vaugier, Isabelle
    Boussaid, Ghilas
    Orlikowski, David
    Prigent, Helene
    Lofaso, Frederic
    RESPIRATORY CARE, 2016, 61 (11) : 1530 - 1535
  • [34] Cardiac assessment of patients with late stage Duchenne muscular dystrophy
    van Bockel, E. A. P.
    Lind, J. S.
    Zijlstra, J. G.
    Wijkstra, P. J.
    Meijer, P. M.
    van den Berg, M. P.
    Slart, R. H. J. A.
    Aarts, L. P. H. J.
    Tulleken, J. E.
    NETHERLANDS HEART JOURNAL, 2009, 17 (06) : 232 - 237
  • [35] Different bone health progression patterns and early-stage risk marker in glucocorticoid-treated ambulatory Duchenne muscular dystrophy
    Zhou, Linyuhan
    Zhou, Hui
    Xu, Huayan
    Sun, Xiaomei
    Chen, Xiaoyong
    Fan, Peicong
    Cai, Xiaotang
    Wang, Qiu
    OSTEOPOROSIS INTERNATIONAL, 2024, 35 (06) : 997 - 1005
  • [36] Quantitative electromyography in ambulatory boys with Duchenne muscular dystrophy
    Verma, Sumit
    Lin, Jenny
    Travers, Curtis
    McCracken, Courtney
    Shah, Durga
    MUSCLE & NERVE, 2017, 56 (06) : 1168 - 1171
  • [37] Safety and efficacy of viltolarsen in ambulatory and nonambulatory males with Duchenne muscular dystrophy
    Harper, Amy D.
    Topaloglu, Haluk
    Mercuri, Eugenio
    Suslov, Vasiliy
    Wu, Liwen
    Ayanoglu, Cigdem Y.
    Tansey, Michael
    Previtera, Michelle L.
    Crozier, Robert A.
    Magnus, Leslie
    Clemens, Paula R.
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [38] Ambulatory Monitoring and Arrhythmic Outcomes in Pediatric and Adolescent Patients With Duchenne Muscular Dystrophy
    Villa, Chet R.
    Czosek, Richard J.
    Ahmed, Humera
    Khoury, Philip R.
    Anderson, Jeffrey B.
    Knilans, Timothy K.
    Jefferies, John L.
    Wong, Brenda
    Spar, David S.
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2016, 5 (01):
  • [39] Early Gross Motor Milestones in Duchenne Muscular Dystrophy
    Norcia, Giulia
    Lucibello, Simona
    Coratti, Giorgia
    Onesimo, Roberta
    Pede, Elisa
    Ferrantini, Gloria
    Brogna, Claudia
    Cicala, Graziamaria
    Carnicella, Sara
    Forcina, Nicola
    Fanelli, Lavinia
    Pane, Marika
    Mercuri, Eugenio
    JOURNAL OF NEUROMUSCULAR DISEASES, 2021, 8 (04) : 453 - 456
  • [40] Multi-Parametric Quantitative MRI in the Early Differential Diagnosis of Ambulatory Children With Duchenne Muscular Dystrophy and Becker Muscular Dystrophy
    Peng, Fei
    Xu, Huayan
    Xu, Ting
    Xu, Ke
    Cai, Xiaotang
    Li, Jiaoyang
    Zhao, Heng
    Liu, Wenhong
    Guo, Yingkun
    Liu, Limin
    JOURNAL OF MAGNETIC RESONANCE IMAGING, 2025,