The daily physiotherapy regimen in cystic fibrosis?

The aim of this paper is to question the accepted physiotherapy regimen for children with Fibrocystic Disease. Is it the most effective way of keeping the lungs clear of secretions? How much are we imposing added stress on an already stressed family? Is it not possible to design a programme which re...

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Main Author: L. M. Davids
Format: Article
Language:English
Published: AOSIS 1986-08-01
Series:South African Journal of Physiotherapy
Subjects:
Online Access:https://sajp.co.za/index.php/sajp/article/view/804
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author L. M. Davids
author_facet L. M. Davids
author_sort L. M. Davids
collection DOAJ
description The aim of this paper is to question the accepted physiotherapy regimen for children with Fibrocystic Disease. Is it the most effective way of keeping the lungs clear of secretions? How much are we imposing added stress on an already stressed family? Is it not possible to design a programme which reduces stress and is socially acceptable? The traditional physiotherapy regimen of breathing exercises, postural drainage and percussion is described. Forced expiratory technique is described as well as various forms of nebulisation. The psychological impact on the family of a chronic, life-threatening disease, is discussed. Compliance with set physiotherapy regimens and the family's (especially the mother's) reaction to them is discussed. The most recent literature on the effectiveness of traditional physiotherapy techniques is reviewed. From this review as well as from personal experience, it is concluded that a rigid physiotherapy regimen is stressful and compliance is frequently poor. Suggestions are made on how to overcome this. It is stressed that this paper deals with the home programme, not with the hospital programme for acute exacerbations of the disease.
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spelling doaj.art-c0db91c72093439584f4cf7bcfc8ff972022-12-22T00:50:07ZengAOSISSouth African Journal of Physiotherapy0379-61752410-82191986-08-01423737610.4102/sajp.v42i3.804667The daily physiotherapy regimen in cystic fibrosis?L. M. Davids0Red Cross War Memorial Children’s HospitalThe aim of this paper is to question the accepted physiotherapy regimen for children with Fibrocystic Disease. Is it the most effective way of keeping the lungs clear of secretions? How much are we imposing added stress on an already stressed family? Is it not possible to design a programme which reduces stress and is socially acceptable? The traditional physiotherapy regimen of breathing exercises, postural drainage and percussion is described. Forced expiratory technique is described as well as various forms of nebulisation. The psychological impact on the family of a chronic, life-threatening disease, is discussed. Compliance with set physiotherapy regimens and the family's (especially the mother's) reaction to them is discussed. The most recent literature on the effectiveness of traditional physiotherapy techniques is reviewed. From this review as well as from personal experience, it is concluded that a rigid physiotherapy regimen is stressful and compliance is frequently poor. Suggestions are made on how to overcome this. It is stressed that this paper deals with the home programme, not with the hospital programme for acute exacerbations of the disease.https://sajp.co.za/index.php/sajp/article/view/804No keywords available
spellingShingle L. M. Davids
The daily physiotherapy regimen in cystic fibrosis?
South African Journal of Physiotherapy
No keywords available
title The daily physiotherapy regimen in cystic fibrosis?
title_full The daily physiotherapy regimen in cystic fibrosis?
title_fullStr The daily physiotherapy regimen in cystic fibrosis?
title_full_unstemmed The daily physiotherapy regimen in cystic fibrosis?
title_short The daily physiotherapy regimen in cystic fibrosis?
title_sort daily physiotherapy regimen in cystic fibrosis
topic No keywords available
url https://sajp.co.za/index.php/sajp/article/view/804
work_keys_str_mv AT lmdavids thedailyphysiotherapyregimenincysticfibrosis
AT lmdavids dailyphysiotherapyregimenincysticfibrosis