Literature DB >> 3171787

Role of conventional physiotherapy in cystic fibrosis.

J J Reisman1, B Rivington-Law, M Corey, J Marcotte, E Wannamaker, D Harcourt, H Levison.   

Abstract

Because of the time and the emotional cost involved in performing daily conventional chest physiotherapy in patients with cystic fibrosis, a 3-year prospective study was undertaken to compare the long-term effects of postural drainage accompanied by percussion and the forced expiratory technique with the effects of the forced expiratory technique alone. Patients who performed the forced expiratory technique alone had mean annual rates of decline that were significantly different from zero for forced expiratory volume in 1 second (p less than 0.001), forced expiratory flow between 25% and 75% of vital capacity (p less than 0.001), and Shwachman clinical score (p less than 0.004). In the group performing conventional physiotherapy with percussion and postural drainage, only the mean annual rate of decline for forced expiratory flow between 25% and 75% of vital capacity was significantly different from zero (p less than 0.03), and it was significantly different from the mean rate of decline associated with the forces expiratory technique alone (p less than 0.04). We conclude that conventional chest physiotherapy should remain a standard component of therapy in cystic fibrosis.

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Year:  1988        PMID: 3171787     DOI: 10.1016/s0022-3476(88)80370-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  19 in total

Review 1.  Cystic fibrosis.

Authors:  P Robinson
Journal:  Thorax       Date:  2001-03       Impact factor: 9.139

Review 2.  Physiotherapy in cystic fibrosis.

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

Review 3.  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 4.  Periodic health examination, 1991 update: 4. Screening for cystic fibrosis. Canadian Task Force on the Periodic Health Examination.

Authors: 
Journal:  CMAJ       Date:  1991-09-15       Impact factor: 8.262

5.  Normal and cystic fibrosis airway surface liquid homeostasis. The effects of phasic shear stress and viral infections.

Authors:  Robert Tarran; Brian Button; Maryse Picher; Anthony M Paradiso; Carla M Ribeiro; Eduardo R Lazarowski; Liqun Zhang; Peter L Collins; Raymond J Pickles; Jeffrey J Fredberg; Richard C Boucher
Journal:  J Biol Chem       Date:  2005-08-08       Impact factor: 5.157

6.  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

Review 7.  Cystic fibrosis: transition from paediatric to adult physician's care.

Authors:  L I Landau
Journal:  Thorax       Date:  1995-10       Impact factor: 9.139

Review 8.  Current concepts in physiotherapy.

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

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

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

Review 10.  Cystic fibrosis.

Authors:  M R Bye; J M Ewig; L M Quittell
Journal:  Lung       Date:  1994       Impact factor: 2.584

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