Lessons learned from a randomized trial of airway secretion clearance techniques in cystic fibrosis
- 9 February 2010
- journal article
- research article
- Published by Wiley in Pediatric Pulmonology
- Vol. 45 (3) , 291-300
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. FEV1 decline, time to need IV antibiotics, and other pulmonary therapies were not different. The annual FEF25–75% 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 FEV1 decline was 1.23% predicted/year.Conclusions: The study was ended early due to dropout and smaller than expected decline in FEV1. Patients were more satisfied with vest and FD. The longitudinal decline in FEF25–75% was faster in vest; we found no other difference in lung function decline, taken together this warrants further study. The slow decline in FEV1 illustrates the difficulty with FEV1 decline as a clinical trial outcome. Pediatr Pulmonol. 2010; 45:291–300.Keywords
Funding Information
- Hill-Rom Inc.
- US Cystic Fibrosis Foundation
This publication has 34 references indexed in Scilit:
- Clinical Use of Ibuprofen is Associated with Slower FEV1 Decline in Children with Cystic FibrosisAmerican Journal of Respiratory and Critical Care Medicine, 2007
- Risk Factors For Rate of Decline in Forced Expiratory Volume in One Second in Children and Adolescents with Cystic FibrosisThe Journal of Pediatrics, 2007
- A multi-method assessment of treatment adherence for children with cystic fibrosisJournal of Cystic Fibrosis, 2006
- Improving rate of decline of FEV1 in young adults with cystic fibrosisThorax, 2006
- Normal and Cystic Fibrosis Airway Surface Liquid HomeostasisJournal of Biological Chemistry, 2005
- Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung diseasePediatric Pulmonology, 2004
- Identifying Treatments That Halt Progression of Pulmonary Disease in Cystic FibrosisPediatric Research, 1997
- Efficacy of the Flutter device for airway mucus clearance in patients with cystic fibrosisThe Journal of Pediatrics, 1994
- Pulmonary function between 6 and 18 years of agePediatric Pulmonology, 1993
- Role of conventional physiotherapy in cystic fibrosisThe Journal of Pediatrics, 1988