Document Detail


Airway clearance therapy in cystic fibrosis patients.
MedLine Citation:
PMID:  19848046     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cystic fibrosis (CF) is the most common life-shortening inherited disease affecting Caucasian people. In CF, the major feature of lung disease is the retention of mucus due to impaired clearance of abnormally viscous airway secretions. Airway clearance techniques (ACTs) may significantly improve mucociliary clearance and gas exchange, thereby being of clinical benefit in reducing pulmonary complications in CF patients. ACTs include conventional chest physiotherapy, active cycle of breathing techniques, autogenic drainage, positive expiratory pressure and high-frequency chest compression. In order to suit the needs of patients, families and care-givers, ACTs need to be individually and continuously adapted.
Authors:
Giovanna Pisi; Alfredo Chetta
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Acta bio-medica : Atenei Parmensis     Volume:  80     ISSN:  0392-4203     ISO Abbreviation:  -     Publication Date:  2009 Aug 
Date Detail:
Created Date:  2009-10-23     Completed Date:  2009-12-11     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101295064     Medline TA:  Acta Biomed     Country:  Italy    
Other Details:
Languages:  eng     Pagination:  102-6     Citation Subset:  IM    
Affiliation:
Cystic Fibrosis Unit, Paediatric Department, University Hospital of Parma, Italy.
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MeSH Terms
Descriptor/Qualifier:
Breathing Exercises*
Chest Wall Oscillation / methods*
Cystic Fibrosis / metabolism,  therapy*
Drainage, Postural / methods*
Humans
Mucus / secretion
Physical Therapy Modalities*
Positive-Pressure Respiration / methods*
Treatment Outcome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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