Literature DB >> 20146387

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

Marci K Sontag1, Alexandra L Quittner, Avani C Modi, Joni M Koenig, Don Giles, Christopher M Oermann, Michael W Konstan, Robert Castile, Frank J Accurso.   

Abstract

RATIONALE: Airway secretion clearance therapies are a cornerstone of cystic fibrosis care, however longitudinal comparative studies are rare. Our objectives were to compare three therapies [postural drainage and percussion: (postural drainage), flutter device (FD), and high frequency chest wall oscillation: (vest)], by studying (1) change in pulmonary function; (2) time to need for intravenous (IV) antibiotics, (3) use of pulmonary therapies, (4) adherence to treatment, (5) treatment satisfaction, and (6) quality of life.
METHODS: Participants were randomly assigned to one of three therapies twice daily. Clinical outcomes were assessed quarterly over 3 years.
RESULTS: Enrollment goals were not met, and withdrawal rates were high, especially in postural drainage (51%) and FD (26%), compared to vest (9%), resulting in early termination. FEV(1) decline, time to need IV antibiotics, and other pulmonary therapies were not different. The annual FEF(25-75%) predicted rate of decline was greater in those using vest (P = 0.02). Adherence was not significantly different (P = 0.09). Overall treatment satisfaction was higher in vest and FD than in postural drainage (P < 0.05). Health-related quality of life was not different. The rate of FEV(1) decline was 1.23% predicted/year.
CONCLUSIONS: The study was ended early due to dropout and smaller than expected decline in FEV(1). Patients were more satisfied with vest and FD. The longitudinal decline in FEF(25-75%) was faster in vest; we found no other difference in lung function decline, taken together this warrants further study. The slow decline in FEV(1) illustrates the difficulty with FEV(1) decline as a clinical trial outcome.

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Year:  2010        PMID: 20146387      PMCID: PMC4163837          DOI: 10.1002/ppul.21179

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


  33 in total

1.  Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease.

Authors:  Timothy D Murphy; Ran D Anbar; Lucille A Lester; Samya Z Nasr; Bruce Nickerson; Donald R VanDevanter; Andrew A Colin
Journal:  Pediatr Pulmonol       Date:  2004-10

2.  Five- to seven-year course of pulmonary function in cystic fibrosis.

Authors:  M Corey; H Levison; D Crozier
Journal:  Am Rev Respir Dis       Date:  1976-12

3.  Tracheal mucus clearance in high-frequency oscillation: effect of peak flow rate bias.

Authors:  M King; A Zidulka; D M Phillips; D Wight; D Gross; H K Chang
Journal:  Eur Respir J       Date:  1990-01       Impact factor: 16.671

4.  Mucus transport by high-frequency nonsymmetrical oscillatory airflow.

Authors:  H K Chang; M E Weber; M King
Journal:  J Appl Physiol (1985)       Date:  1988-09

5.  Changes in the normal maximal expiratory flow-volume curve with growth and aging.

Authors:  R J Knudson; M D Lebowitz; C J Holberg; B Burrows
Journal:  Am Rev Respir Dis       Date:  1983-06

6.  Long-term comparative trial of positive expiratory pressure versus oscillating positive expiratory pressure (flutter) physiotherapy in the treatment of cystic fibrosis.

Authors:  P M McIlwaine; L T Wong; D Peacock; A G Davidson
Journal:  J Pediatr       Date:  2001-06       Impact factor: 4.406

7.  Annual lung function changes in young patients with chronic lung disease.

Authors:  P J F M Merkus; H A W M Tiddens; J C de Jongste
Journal:  Eur Respir J       Date:  2002-05       Impact factor: 16.671

Review 8.  Pathophysiology and management of pulmonary infections in cystic fibrosis.

Authors:  Ronald L Gibson; Jane L Burns; Bonnie W Ramsey
Journal:  Am J Respir Crit Care Med       Date:  2003-10-15       Impact factor: 21.405

9.  Role of conventional physiotherapy in cystic fibrosis.

Authors:  J J Reisman; B Rivington-Law; M Corey; J Marcotte; E Wannamaker; D Harcourt; H Levison
Journal:  J Pediatr       Date:  1988-10       Impact factor: 4.406

10.  Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis.

Authors:  Avani C Modi; Alexandra L Quittner
Journal:  J Pediatr Psychol       Date:  2003-12
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  13 in total

1.  Oscillating devices for airway clearance in people with cystic fibrosis.

Authors:  Lisa Morrison; Stephanie Milroy
Journal:  Cochrane Database Syst Rev       Date:  2020-04-30

Review 2.  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

3.  A Comparison between Two Pathophysiologically Different yet Microbiologically Similar Lung Diseases: Cystic Fibrosis and Chronic Obstructive Pulmonary Disease.

Authors:  Daniel E Fenker; Cameron T McDaniel; Warunya Panmanee; Ralph J Panos; Eric J Sorscher; Carleen Sabusap; John P Clancy; Daniel J Hassett
Journal:  Int J Respir Pulm Med       Date:  2018-11-29

4.  Objective Versus Self-Reported Adherence to Airway Clearance Therapy in Cystic Fibrosis.

Authors:  Gabriela R Oates; Irena Stepanikova; Steven M Rowe; Stephanie Gamble; Hector H Gutierrez; William T Harris
Journal:  Respir Care       Date:  2018-12-11       Impact factor: 2.258

5.  Parents as equal partners in the paediatric cystic fibrosis multidisciplinary team.

Authors:  Mandy Bryon; Colin Wallis
Journal:  J R Soc Med       Date:  2011-07       Impact factor: 5.344

Review 6.  Oscillating devices for airway clearance in people with cystic fibrosis.

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

7.  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

8.  Clinician's Commentary on Morgan et al.(1).

Authors:  Jennifer L Agnew
Journal:  Physiother Can       Date:  2015       Impact factor: 1.037

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.  Short-term effects of high-frequency chest compression and positive expiratory pressure in patients with cystic fibrosis.

Authors:  Valentina Fainardi; Francesco Longo; Silvia Faverzani; Maria Candida Tripodi; Alfredo Chetta; Giovanna Pisi
Journal:  J Clin Med Res       Date:  2011-11-10
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