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Research ArticleConference Proceedings

Cystic Fibrosis: Current Trends in Respiratory Care

Jeffrey S Wagener and Aree A Headley
Respiratory Care March 2003, 48 (3) 234-247;
Jeffrey S Wagener
Department of Pediatrics, University of Colorado School of Medicine, and The Children's Hospital, Denver, Colorado
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Aree A Headley
Department of Pediatrics, University of Colorado School of Medicine, and The Children's Hospital, Denver, Colorado
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Abstract

Cystic fibrosis is a genetic disease that typically produces malnutrition and chronic respiratory infections. Prolonged bronchial obstruction, infection, and inflammation result in bronchiectstasis and permanent lung damage. Most cystic fibrosis patients die because of this progressive respiratory disease. Thus, in the absence of a cure, effective respiratory therapy is the primary means to extend and improve the quality of life for the cystic fibrosis patient. Aerosol therapy, airway clearance techniques, and noninvasive ventilation can all improve quality of life and possibly extend survival. Close patient monitoring with pulmonary function testing, chest radiography, and induced sputum can result in earlier treatment, potentially reducing permanent lung damage. Earlier diagnosis has prevented serious complications through early initiation of preventive therapies such as improved nutrition.

  • pediatric
  • respiratory
  • pulmonary
  • cystic fibrosis
  • respiratory care
  • airway clearance

Footnotes

  • Correspondence: Jeffrey S Wagener MD, Children's Hospital B-395, 1056 E 19th Avenue, Denver CO 80218.
  • Jeffrey S Wagener MD presented a version of this report at the 31st Respiratory Care Journal Conference, Current Trends in Neonatal and Pediatric Respiratory Care Conference, August 16-18, 2002, in Keystone, Colorado.

  • Copyright © 2003 by Daedalus Enterprises Inc.
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Respiratory Care: 48 (3)
Respiratory Care
Vol. 48, Issue 3
1 Mar 2003
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Cystic Fibrosis: Current Trends in Respiratory Care
Jeffrey S Wagener, Aree A Headley
Respiratory Care Mar 2003, 48 (3) 234-247;

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Cystic Fibrosis: Current Trends in Respiratory Care
Jeffrey S Wagener, Aree A Headley
Respiratory Care Mar 2003, 48 (3) 234-247;
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Keywords

  • Pediatric
  • respiratory
  • pulmonary
  • cystic fibrosis
  • respiratory care
  • airway clearance

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