» Articles » PMID: 21289861

Physiotherapeutic Management Strategies for the Treatment of Cystic Fibrosis in Adults

Overview
Publisher Dove Medical Press
Specialty Health Services
Date 2011 Feb 4
PMID 21289861
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Physiotherapy has long been considered a cornerstone of condition management for people with cystic fibrosis (CF). The presentation of CF has changed over time with an increased life expectancy and increased expectations of people with CF to have a complete lifestyle. In turn, the scope of strategies used in physiotherapy for CF have also changed dramatically over the years, moving away from routine postural drainage and manual techniques toward an individualized regimen including the choice of many different forms of airway clearance, such as both independent and assisted, exercise, treatments to promote continence and good posture, inhalation therapy, oxygen, and noninvasive ventilation. This article describes the techniques and overall strategies used by physiotherapists in helping people with CF to manage the symptoms and progression of their condition.

Citing Articles

Personalising airway clearance in chronic suppurative lung diseases: a scoping review.

Schofield L, Singh S, Yousaf Z, Wild J, Hind D ERJ Open Res. 2023; 9(3).

PMID: 37342087 PMC: 10277870. DOI: 10.1183/23120541.00010-2023.


Efficacy of the Simeox Airway Clearance Technology in the Homecare Treatment of Children with Clinically Stable Cystic Fibrosis: A Randomized Controlled Trial.

Sands D, Walicka-Serzysko K, Milczewska J, Postek M, Jeneralska N, Cichocka A Children (Basel). 2023; 10(2).

PMID: 36832333 PMC: 9955024. DOI: 10.3390/children10020204.


Manual therapies in cystic fibrosis care: a scoping review.

Sposato Sinderholm N, Bjersa K Chiropr Man Therap. 2023; 31(1):7.

PMID: 36747207 PMC: 9903555. DOI: 10.1186/s12998-023-00478-0.


The clinical effects of combining postural exercises with chest physiotherapy in cystic fibrosis: A single-blind, randomized-controlled trial.

Gungor S, Gencer-Atalay K, Bahar-Ozdemir Y, Kenis-Coskun O, Karadag-Saygi E Turk J Phys Med Rehabil. 2021; 67(1):91-98.

PMID: 33948549 PMC: 8088798. DOI: 10.5606/tftrd.2021.5214.

References
1.
Konstan M, Stern R, DOERSHUK C . Efficacy of the Flutter device for airway mucus clearance in patients with cystic fibrosis. J Pediatr. 1994; 124(5 Pt 1):689-93. DOI: 10.1016/s0022-3476(05)81356-3. View

2.
Chatham K, Ionescu A, Nixon L, Shale D . A short-term comparison of two methods of sputum expectoration in cystic fibrosis. Eur Respir J. 2004; 23(3):435-9. DOI: 10.1183/09031936.04.00084904. View

3.
Francis P, Muller N, Gurwitz D, Milligan D, Levison H, Bryan A . Hemoglobin desaturation: its occurrence during sleep in patients with cystic fibrosis. Am J Dis Child. 1980; 134(8):734-40. DOI: 10.1001/archpedi.1980.02130200004002. View

4.
van der Schans C, Prasad A, Main E . Chest physiotherapy compared to no chest physiotherapy for cystic fibrosis. Cochrane Database Syst Rev. 2000; (2):CD001401. DOI: 10.1002/14651858.CD001401. View

5.
van der Giessen L, de Jongste J, Gosselink R, Hop W, Tiddens H . RhDNase before airway clearance therapy improves airway patency in children with CF. Pediatr Pulmonol. 2007; 42(7):624-30. DOI: 10.1002/ppul.20636. View