Literature DB >> 15674888

Conventional chest physiotherapy compared to other airway clearance techniques for cystic fibrosis.

E Main1, A Prasad, C Schans.   

Abstract

BACKGROUND: Cystic fibrosis is an inherited life-limiting disorder, characterised by pulmonary infections and thick airway secretions. Chest physiotherapy has been integral to clinical management in facilitating removal of airway secretions. Conventional chest physiotherapy techniques (CCPT) have depended upon assistance during treatments, while more contemporary airway clearance techniques are self-administered, facilitating independence and flexibility.
OBJECTIVES: To compare CCPT with other airway clearance techniques in terms of their effects on respiratory function, individual preference, adherence, quality of life and other outcomes. SEARCH STRATEGY: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group trials register which comprises references identified from comprehensive electronic database searches and handsearching of relevant journals and abstract books of conference proceedings. We also searched CINAHL from 1982 to 2002 and AMED from 1985 to 2002. Date of most recent search: January 2004. SELECTION CRITERIA: Randomised or quasi-randomised clinical trials including those with a cross-over design where CCPT was compared with other airway clearance techniques. Studies of less than seven days duration were excluded. DATA COLLECTION AND ANALYSIS: Two reviewers allocated quality scores to relevant studies and independently extracted data. If we were unable to extract data, we invited authors to submit their data. We excluded studies from meta-analysis when data were lost or study design precluded comparison. For some continuous outcomes, we used the generic inverse variance method for meta-analysis of data from cross-over trials and data from parallel-designed trials were incorporated for comparison. We also examined efficacy of specific techniques and effects of treatment duration. MAIN
RESULTS: Seventy-eight publications were identified by the searches. Twenty-nine of these were included, representing 15 data sets with 475 participants. There was no difference between CCPT and other airway clearance techniques in terms of respiratory function measured by standard lung function tests. Studies undertaken during acute exacerbations demonstrated relatively large gains in respiratory function irrespective of airway clearance technique. Longer-term studies demonstrated smaller improvements or deterioration over time. Ten studies reported individual preferences for technique, with participants tending to favour self-administered techniques. Heterogeneity in the measurement of preference precluded these data from meta-analysis. AUTHORS'
CONCLUSIONS: This review demonstrated no advantage of CCPT over other airway clearance techniques in terms of respiratory function. There was a trend for participants to prefer self-administered airway clearance techniques. Limitations of this review included a paucity of well-designed, adequately-powered, long-term trials.

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Mesh:

Year:  2005        PMID: 15674888      PMCID: PMC7388307          DOI: 10.1002/14651858.CD002011.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  48 in total

1.  A comparison of bronchial drainage treatments in cystic fibrosis.

Authors:  J Kluft; L Beker; M Castagnino; J Gaiser; H Chaney; R J Fink
Journal:  Pediatr Pulmonol       Date:  1996-10

2.  Current understanding of the inflammatory process in cystic fibrosis: onset and etiology.

Authors:  M W Konstan; M Berger
Journal:  Pediatr Pulmonol       Date:  1997-08

3.  Face mask physiotherapy in cystic fibrosis.

Authors:  J C Tyrrell; E J Hiller; J Martin
Journal:  Arch Dis Child       Date:  1986-06       Impact factor: 3.791

4.  Benefits of music therapy as an adjunct to chest physiotherapy in infants and toddlers with cystic fibrosis.

Authors:  M C Grasso; B M Button; D J Allison; S M Sawyer
Journal:  Pediatr Pulmonol       Date:  2000-05

5.  Comparison of effects of an intrapulmonary percussive ventilator to standard aerosol and chest physiotherapy in treatment of cystic fibrosis.

Authors:  D N Homnick; F White; C de Castro
Journal:  Pediatr Pulmonol       Date:  1995-07

6.  Comparison of manual and mechanical chest percussion in hospitalized patients with cystic fibrosis.

Authors:  M L Bauer; J McDougal; R A Schoumacher
Journal:  J Pediatr       Date:  1994-02       Impact factor: 4.406

7.  The immediate effect of physiotherapy and aerosol treatment on pulmonary function in children with cystic fibrosis.

Authors:  K F Kerrebijn; R Veentjer; E Bonzet-vd Water
Journal:  Eur J Respir Dis       Date:  1982-01

8.  Efficacy of the Flutter device for airway mucus clearance in patients with cystic fibrosis.

Authors:  M W Konstan; R C Stern; C F Doershuk
Journal:  J Pediatr       Date:  1994-05       Impact factor: 4.406

9.  A short-term comparison of two methods of sputum expectoration in cystic fibrosis.

Authors:  K Chatham; A A Ionescu; L S Nixon; D J Shale
Journal:  Eur Respir J       Date:  2004-03       Impact factor: 16.671

10.  Relative effects of bronchial drainage and exercise for in-hospital care of patients with cystic fibrosis.

Authors:  F J Cerny
Journal:  Phys Ther       Date:  1989-08
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Journal:  Cochrane Database Syst Rev       Date:  2016-12-22

Review 3.  Singing as an adjunct therapy for children and adults with cystic fibrosis.

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4.  What Does the Cochrane Collaboration Say about Respiratory Physiotherapy?

Authors: 
Journal:  Physiother Can       Date:  2012-04-05       Impact factor: 1.037

5.  Lessons learned from a randomized trial of airway secretion clearance techniques in cystic fibrosis.

Authors:  Marci K Sontag; Alexandra L Quittner; Avani C Modi; Joni M Koenig; Don Giles; Christopher M Oermann; Michael W Konstan; Robert Castile; Frank J Accurso
Journal:  Pediatr Pulmonol       Date:  2010-03

6.  Respiratory physical therapy techniques recommended for patients with cystic fibrosis treated in specialized centers.

Authors:  Márcio Vinícius Fagundes Donadio; Natália Evangelista Campos; Fernanda Maria Vendrusculo; Augusta Machado Stofella; Ana Carolina da Silva Almeida; Bruna Ziegler; Camila Isabel Santos Schivinski; Cíntia Helena Santuzzi; Edilene do Socorro Nascimento Falcão Sarges; Fernanda Mayrink Gonçalves; Maria Ângela Gonçalves de Oliveira Ribeiro; Nelbe Nesi Santana; Sarah Bezerra de Paiva; Vanessa Cristina Waetge Pires de Godoy; Evanirso da Silva Aquino
Journal:  Braz J Phys Ther       Date:  2019-11-29       Impact factor: 3.377

Review 7.  Oscillating devices for airway clearance in people with cystic fibrosis.

Authors:  Lisa Morrison; Stephanie Innes
Journal:  Cochrane Database Syst Rev       Date:  2017-05-04

Review 8.  The Evolution of Cystic Fibrosis Care.

Authors:  Jessica E Pittman; Thomas W Ferkol
Journal:  Chest       Date:  2015-08       Impact factor: 9.410

9.  Airway clearance devices for cystic fibrosis: an evidence-based analysis.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2009-11-01

10.  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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