Adherence to Airway Clearance Therapies by Adult Cystic Fibrosis Patients

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Adherence to airway clearance therapies by adult cystic fibrosis patients.

BACKGROUND Airway clearance therapy (ACT) is critical in cystic fibrosis (CF). OBJECTIVES To determine rates of self-reported adherence to ACT by patients treated in an adult CF program, to identify patient characteristics associated with poor adherence, to typify adherence according to ACT technique, and to indicate reasons for poor adherence. METHODS Our cross-sectional study included CF ...

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Cystic fibrosis pulmonary guidelines: airway clearance therapies.

Cystic fibrosis (CF) is a genetic disease characterized by dehydration of airway surface liquid and impaired mucociliary clearance. As a result, there is difficulty clearing pathogens from the lung, and patients experience chronic pulmonary infections and inflammation. Clearance of airway secretions has been a primary therapy for those with CF, and a variety of airway clearance therapies (ACTs)...

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Special Articles Cystic Fibrosis Pulmonary Guidelines: Airway Clearance Therapies

Cystic fibrosis (CF) is a genetic disease characterized by dehydration of airway surface liquid and impaired mucociliary clearance. As a result, there is difficulty clearing pathogens from the lung, and patients experience chronic pulmonary infections and inflammation. Clearance of airway secretions has been a primary therapy for those with CF, and a variety of airway clearance therapies (ACTs)...

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Treatment Adherence: Airway Clearance Therapy in Cystic Fibrosis

In CF, as in other chronic, ultimately fatal disorders, therapeutic goals are most often compromised by poor treatment adherence. Both clinical experience and formal studies indicate that in CF, patients comply with about 50% of their prescribed treatments. However, the significance of that figure is distorted by the fact that compliance with individual components of the therapeutic regimen var...

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Airway clearance in cystic fibrosis.

Airway clearance is considered an integral component of standard therapy for cystic fibrosis (CF) patients. Although the pathophysiology of CF has not been conclusively delineated, most of the theories revolve around the development of viscous airway secretions.1–4 These secretions are thought to be poorly cleared from the lung, leading to airway obstruction and infection with Staphylococcus au...

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ژورنال

عنوان ژورنال: Respiratory Care

سال: 2013

ISSN: 0020-1324,1943-3654

DOI: 10.4187/respcare.01389