Literature DB >> 17322959

Physiotherapeutic conduct in amyotrophic lateral sclerosis.

Andreza Martinez Pozza1, Milene Karenine Delamura, Clarissa Ramirez, Nelson Iguimar Valério, Laís Helena Carvalho Marino, Neuseli Marino Lamari.   

Abstract

Amyotrophic Lateral Sclerosis (ALS) is a fatal progressive neurodegenerative disease with multifactorial etiology for which, so far, there is no effective medicinal treatment. However, by means of kinesiotherapy intervention and patient guidance and care, physiotherapy can delay physical functional losses, muscle fatigue and immobility of the joint-muscle system, thereby improving the quality of life. This survey had the aim of reviewing the physiotherapeutic conduct currently used in ALS cases. Monthly monitoring is recommended, with changes in goals and conduct at each stage of the disease, activities to be pursued around the home, and emphasis on stretching, muscle strengthening, posture adequacy and respiratory kinesiotherapy.

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Year:  2006        PMID: 17322959     DOI: 10.1590/s1516-31802006000600011

Source DB:  PubMed          Journal:  Sao Paulo Med J        ISSN: 1516-3180            Impact factor:   1.044


  1 in total

1.  Upper extremity orthoses use in amyotrophic lateral sclerosis/motor neuron disease: three case reports.

Authors:  Cindy C Ivy; Susan M Smith; Miranda M Materi
Journal:  Hand (N Y)       Date:  2014-12
  1 in total

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