Kinesitherapy in amyotrophic lateral sclerosis

Introduction and purpose of work. Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of unknown etiology. As a result, damage to motor neurons in patients with clinical symptoms such as weakness and atrophy of muscles, spasticity, paresis, disorders of speech and swallowi...

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Main Author: Joanna Iłżecka
Format: Article
Language:English
Published: Kazimierz Wielki University 2017-12-01
Series:Journal of Education, Health and Sport
Subjects:
Online Access:http://www.ojs.ukw.edu.pl/index.php/johs/article/view/5102
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spelling doaj-c0983a936664462e9ba83b58587ea2b22020-11-25T01:41:21ZengKazimierz Wielki UniversityJournal of Education, Health and Sport2391-83062017-12-01712839310.5281/zenodo.10986604773Kinesitherapy in amyotrophic lateral sclerosisJoanna Iłżecka0Independent Neurological Rehabilitation Unit, Medical University of LublinIntroduction and purpose of work. Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of unknown etiology. As a result, damage to motor neurons in patients with clinical symptoms such as weakness and atrophy of muscles, spasticity, paresis, disorders of speech and swallowing difficulties. In view of the lack of effective treatment, it is important causal symptomatic treatment and rehabilitation, including kinesitherapy. The aim of this study was to review the literature concerning the use of kinesitherapy in the ALS. Brief description of the state of knowledge. The evidence regarding the benefits of kinesitherapy in the ALS is limited to a few experimental studies and clinical trials. Experimental studies confirm the beneficial neuroprotective effect of kinesitherapy on motoneurons. Clinical trials have shown the beneficial effect of moderate exercise on the state of ALS patients. It is recommended to exercise: stretching, aerobic, resistance, strengthening and balance, as well as special methods such as the method Vojta and PNF. Literature data show that exercise influence on the activity of motoneurons which are more resistant to apoptosis selectively. Summary. Kinesitherapy is recommended for patients already in the early stages of ALS. However, despite the presented advantages of this method are the need for a more randomized trials on a larger group of patients.http://www.ojs.ukw.edu.pl/index.php/johs/article/view/5102amyotrophic lateral sclerosis, nervous system, kinesitherapy, neuroprotection
collection DOAJ
language English
format Article
sources DOAJ
author Joanna Iłżecka
spellingShingle Joanna Iłżecka
Kinesitherapy in amyotrophic lateral sclerosis
Journal of Education, Health and Sport
amyotrophic lateral sclerosis, nervous system, kinesitherapy, neuroprotection
author_facet Joanna Iłżecka
author_sort Joanna Iłżecka
title Kinesitherapy in amyotrophic lateral sclerosis
title_short Kinesitherapy in amyotrophic lateral sclerosis
title_full Kinesitherapy in amyotrophic lateral sclerosis
title_fullStr Kinesitherapy in amyotrophic lateral sclerosis
title_full_unstemmed Kinesitherapy in amyotrophic lateral sclerosis
title_sort kinesitherapy in amyotrophic lateral sclerosis
publisher Kazimierz Wielki University
series Journal of Education, Health and Sport
issn 2391-8306
publishDate 2017-12-01
description Introduction and purpose of work. Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of unknown etiology. As a result, damage to motor neurons in patients with clinical symptoms such as weakness and atrophy of muscles, spasticity, paresis, disorders of speech and swallowing difficulties. In view of the lack of effective treatment, it is important causal symptomatic treatment and rehabilitation, including kinesitherapy. The aim of this study was to review the literature concerning the use of kinesitherapy in the ALS. Brief description of the state of knowledge. The evidence regarding the benefits of kinesitherapy in the ALS is limited to a few experimental studies and clinical trials. Experimental studies confirm the beneficial neuroprotective effect of kinesitherapy on motoneurons. Clinical trials have shown the beneficial effect of moderate exercise on the state of ALS patients. It is recommended to exercise: stretching, aerobic, resistance, strengthening and balance, as well as special methods such as the method Vojta and PNF. Literature data show that exercise influence on the activity of motoneurons which are more resistant to apoptosis selectively. Summary. Kinesitherapy is recommended for patients already in the early stages of ALS. However, despite the presented advantages of this method are the need for a more randomized trials on a larger group of patients.
topic amyotrophic lateral sclerosis, nervous system, kinesitherapy, neuroprotection
url http://www.ojs.ukw.edu.pl/index.php/johs/article/view/5102
work_keys_str_mv AT joannaiłzecka kinesitherapyinamyotrophiclateralsclerosis
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