Literature DB >> 2044730

Chest physiotherapy in hospitalized patients with cystic fibrosis: a study of lung function effects and sputum production.

B Oberwaldner1, B Theissl, A Rucker, M S Zach.   

Abstract

In order to evaluate the short-term lung function effects of high-pressure positive expiratory pressure (PEP)-mask physiotherapy (PT) in relation to PT-assisted sputum production, we studied 18 patients with cystic fibrosis (CF), hospitalized for a pulmonary exacerbation. Lung functions were measured before (a) and after PT (b) on day one (1), five (2), ten (3) and fifteen (4). Five functions improved significantly from a1 to b1, eight from a2 to b2, seven from a3 to b3, and seven from a4 to b4. Baseline (a) measurements improved only slightly, but post-PT (b) values improved more markedly from 1 to 4, and this improvement reached statistical significance for six functions; consequently, a-to-b lung function changes tended to increase from investigation 1 to 4. Eleven PT-induced lung function changes correlated to the weight of sputum produced. High-pressure PEP-mask PT therefore resulted in significant lung function improvements, and not only maintained but increased its effect in the course of the hospitalization.

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Year:  1991        PMID: 2044730

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  11 in total

Review 1.  Physiotherapy in cystic fibrosis.

Authors:  S A Prasad; E L Tannenbaum; C Mikelsons
Journal:  J R Soc Med       Date:  2000       Impact factor: 5.344

2.  Effect of positive expiratory pressure breathing in patients with cystic fibrosis.

Authors:  M S Zach; B Oberwaldner
Journal:  Thorax       Date:  1992-01       Impact factor: 9.139

Review 3.  Structure and function of the mucus clearance system of the lung.

Authors:  Brenda M Button; Brian Button
Journal:  Cold Spring Harb Perspect Med       Date:  2013-08-01       Impact factor: 6.915

Review 4.  Positive expiratory pressure therapy versus other airway clearance techniques for bronchiectasis.

Authors:  Annemarie L Lee; Angela T Burge; Anne E Holland
Journal:  Cochrane Database Syst Rev       Date:  2017-09-27

Review 5.  The role of recombinant human DNase in the treatment of patients with cystic fibrosis: many promises, more problems.

Authors:  M S Zach
Journal:  Thorax       Date:  1996-07       Impact factor: 9.139

Review 6.  Current concepts in physiotherapy.

Authors:  S A Prasad
Journal:  J R Soc Med       Date:  1993       Impact factor: 5.344

7.  Self-administered chest physiotherapy in cystic fibrosis: a comparative study of high-pressure PEP and autogenic drainage.

Authors:  A Pfleger; B Theissl; B Oberwaldner; M S Zach
Journal:  Lung       Date:  1992       Impact factor: 2.584

8.  Current devices of respiratory physiotherapy.

Authors:  A Hristara-Papadopoulou; J Tsanakas; G Diomou; O Papadopoulou
Journal:  Hippokratia       Date:  2008       Impact factor: 0.471

Review 9.  Chest physiotherapy compared to no chest physiotherapy for cystic fibrosis.

Authors:  Louise Warnock; Alison Gates
Journal:  Cochrane Database Syst Rev       Date:  2015-12-21

10.  Effects of chest physiotherapy and aerobic exercise training on physical fitness in young children with cystic fibrosis.

Authors:  Bulent Elbasan; Nur Tunali; Irem Duzgun; Ugur Ozcelik
Journal:  Ital J Pediatr       Date:  2012-01-10       Impact factor: 2.638

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