Noninvasive Ventilation and Respiratory Physical Therapy for Amyotrophic Lateral Sclerosis patients

Authors

  • Bruno Presto Fisioterapeuta, Professor de Fisioterapia Respiratória do Centro Universitário metodista Bennett (UNIBENNETT) e Universidade Gama Filho (UGF), Rio de Janeiro, RJ.
  • Marco Orsini Graduando em Medicina, Professor Titular do Programa de Iniciação Científica da Escola Superior de Ensino Helena Antipoff (ESEHA) e Doutorando em Neurologia/Neurociências na Universidade Federal Fluminense – UFF, Niterói, RJ
  • Luciana DN Presto Fisioterapeuta, Professora de Fisioterapia Cardiológica da UNIBENNETT, Rio de Janeiro, RJ
  • Miriam Calheiros Fisioterapeuta, Professora Titular de Neuropediatria – ESEHA, Niterói, RJ.
  • Marcos RG de Freitas Professor Titular e Chefe do Serviço de Neurologia da UFF, Niterói, RJ.
  • Mariana P Mello Fisioterapeuta, Programa de Iniciação Científica do Serviço de Neurologia na UFF, Niterói, RJ
  • Carlos HM Reis Neurologista e Professor Titular da Faculdade de Medicina de Valença, Valença, RJ
  • Osvaldo JM Nascimento Professor Titular e Coordenador da Pós-Graduação em Neurologia/Neurociências da UFF, Niterói, RJ.

DOI:

https://doi.org/10.34024/rnc.2009.v17.8555

Keywords:

Amyotrophic Lateral Sclerosis, Ventilation, Physical Therapy

Abstract

The Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative illness, progressive and lethal that generally leads to the death five years after the beginning of the first symptoms. Of this form, the palliative care must begin soon after the confirmation of the clinical diagnosis. At present, the only medication approved for the treatment of the illness, the Riluzole, seems to contribute for the prolongation of the survival of the patients in a period of two the three months. All of the skeletal muscles are affected on the illness progresses, including the respiratory muscles. Objective. To guide the health professionals about the utilization of the Noninvasive Ventilation (NIV) and respiratory physiotherapy in patients with ALS, as well as its indication. Method. Update of articles about NIV and of the respiratory physiotherapy in patients with ALS, in the last years in the data bases Medline, SciELO, Cochrane and Lilacs. Conclusion. The NIV can prolong the survival and improve the quality of life of the patients with ALS during the course of the illness. Moreover, the management of the respiratory muscles, when applied in a care way, improves the pulmonary function, minimizes the decline of the current volume and delays the beginning of the respiratory insufficiency.

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References

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Published

2009-09-30

Issue

Section

Atualização

How to Cite

1.
Presto B, Orsini M, Presto LD, Calheiros M, Freitas MR de, Mello MP, et al. Noninvasive Ventilation and Respiratory Physical Therapy for Amyotrophic Lateral Sclerosis patients. Rev Neurocienc [Internet]. 2009 Sep. 30 [cited 2025 Dec. 15];17(3):293-7. Available from: https://periodicos.unifesp.br/index.php/neurociencias/article/view/8555