Literature DB >> 3543830

Forced expirations against a variable resistance: a new chest physiotherapy method in cystic fibrosis.

B Oberwaldner, J C Evans, M S Zach.   

Abstract

Twenty patients with cystic fibrosis (CF) were trained to mobilize intrabronchial secretions by a new method of positive expiratory pressure mask (PEP mask) physiotherapy (PT). Patients repeatedly expired forcefully through the PEP mask; expiratory resistance was varied by eight different internal diameter resistors at the outlet. Forced vital capacity with the mask (FVCPEP) was determined for each resistor and was compared with the one measured without the instrument (FVC); simultaneously the sustained expiratory pressure (SEP) developed against the resistance was recorded. After training, each patient exceeded FVC with one or more resistors; "optimum" FVCPEP was 124 +/- 16% FVC at a SEP of 61 +/- 21 cm H2O. Using the PEP mask, patients cleared a higher percentage of their daily sputum volume than with conventional PT (78 +/- 22% versus 53 +/- 17%, p less than 0.01). In 11 patients (subgroup 1), multiple aspects of lung function were measured at the beginning of the study, after 10 months with PEP mask PT, after two further months without using the mask but with conventional PT, and after six more months with PEP mask PT. Results showed significantly increased expiratory flow rates, significantly decreased hyperinflation and airway instability with PEP mask PT, and a marked decline of lung function without it. The remaining nine patients (subgroup 2) entered into the same protocol; based on findings in subgroup 1 and on ethical considerations, however, the control period without PEP mask PT was then omitted, resulting in a steady and statistically significant improvement of lung function over the entire observation period. In the course of preliminary trials, two children transiently used a suboptimal resistance (FVCPEP less than FVC) and responded with a deterioration of lung function. By dilating airways and evacuating trapped gas, this method of PEP mask PT improves lung function and mucus clearance in CF. Thorough practice with the technique and frequent control of the optimal resistance are mandatory.

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Mesh:

Year:  1986        PMID: 3543830     DOI: 10.1002/ppul.1950020608

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  29 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.  Non-invasive ventilation assists chest physiotherapy in adults with acute exacerbations of cystic fibrosis.

Authors:  A E Holland; L Denehy; G Ntoumenopoulos; M T Naughton; J W Wilson
Journal:  Thorax       Date:  2003-10       Impact factor: 9.139

3.  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

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

Authors:  C P van der Schans; T W van der Mark; G de Vries; D A Piers; H Beekhuis; J E Dankert-Roelse; D S Postma; G H Koëter
Journal:  Thorax       Date:  1991-04       Impact factor: 9.139

Review 5.  Pathogenesis and management of lung disease in cystic fibrosis.

Authors:  M S Zach
Journal:  J R Soc Med       Date:  1991       Impact factor: 5.344

Review 6.  Autogenic drainage: a modern approach to physiotherapy in cystic fibrosis.

Authors:  M H Schöni
Journal:  J R Soc Med       Date:  1989       Impact factor: 5.344

Review 7.  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

8.  Oscillatory positive expiratory pressure treatment in lower respiratory tract infection.

Authors:  Yingmeng Ni; Lin Ding; Youchao Yu; Ranran Dai; Hong Chen; Guochao Shi
Journal:  Exp Ther Med       Date:  2018-08-01       Impact factor: 2.447

Review 9.  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

10.  Chest physiotherapy in cystic fibrosis: a comparative study of autogenic drainage and the active cycle of breathing techniques with postural drainage.

Authors:  S Miller; D O Hall; C B Clayton; R Nelson
Journal:  Thorax       Date:  1995-02       Impact factor: 9.139

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