Literature DB >> 7701456

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

S Miller1, D O Hall, C B Clayton, R Nelson.   

Abstract

BACKGROUND--Autogenic drainage has been suggested as an alternative method of chest physiotherapy in patients with cystic fibrosis. In this study autogenic drainage was compared with the active cycle of breathing techniques (ACBT) together with postural drainage. METHODS--Eighteen patients with cystic fibrosis took part in a randomised two-day crossover trial. There were two sessions of one method of physiotherapy on each day, either autogenic drainage or ACBT. The study days were one week apart. On each day the patients were monitored for six hours. Mucus movement was quantified by a radioaerosol technique. Airway clearance was studied qualitatively using xenon-133 scintigraphic studies at the start and end of each day. Expectorated sputum was collected during and for one hour after each session of physiotherapy. Pulmonary functions tests were performed before and after each session. Oxygen saturation (SaO2) and heart rate were measured before, during, and after each session. RESULTS--Autogenic drainage cleared mucus from the lungs faster than ACBT over the whole day. Both methods improved ventilation, as assessed by the xenon-133 ventilation studies. No overall differences were found in the pulmonary function test results, but more patients had an improved forced expiratory flow from 25% to 75% with autogenic drainage, while more showed an improved forced vital capacity with ACBT. No differences were found in sputum weight and heart rate, nor in mean SaO2 over the series, but four patients desaturated during ACBT. CONCLUSIONS--Autogenic drainage was found to be as good as ACBT at clearing mucus in patients with cystic fibrosis and is therefore an effective method of home physiotherapy. Patients with cystic fibrosis should be assessed as to which method suits them best.

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Year:  1995        PMID: 7701456      PMCID: PMC473916          DOI: 10.1136/thx.50.2.165

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  21 in total

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Journal:  Lung       Date:  1992       Impact factor: 2.584

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  14 in total

Review 1.  Cystic fibrosis--an Indian perspective on recent advances in diagnosis and management.

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Journal:  Indian J Pediatr       Date:  1996 Mar-Apr       Impact factor: 1.967

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

Review 4.  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

5.  Effects of Autogenic Drainage on Sputum Recovery and Pulmonary Function in People with Cystic Fibrosis: A Systematic Review.

Authors:  Kimbly Morgan; Kristin Osterling; Robert Gilbert; Gail Dechman
Journal:  Physiother Can       Date:  2015       Impact factor: 1.037

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

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Authors:  Tracey Daniels
Journal:  J Multidiscip Healthc       Date:  2010-11-19

8.  Airway clearance techniques for cystic fibrosis: an overview of Cochrane systematic reviews.

Authors:  Lisa M Wilson; Lisa Morrison; Karen A Robinson
Journal:  Cochrane Database Syst Rev       Date:  2019-01-24

Review 9.  Autogenic drainage for airway clearance in cystic fibrosis.

Authors:  Pamela McCormack; Paul Burnham; Kevin W Southern
Journal:  Cochrane Database Syst Rev       Date:  2017-10-06

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Authors:  Naomi A Mckoy; Lisa M Wilson; Ian J Saldanha; Olaide A Odelola; Karen A Robinson
Journal:  Cochrane Database Syst Rev       Date:  2016-07-05
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