Monitoring of structure and function in early cystic fibrosis lung disease

Sarath C. Ranganathan, Stephanie D. Davis, Margaret Rosenfeld

Research output: Contribution to journalArticle

1 Scopus citations


Concurrent with improving survival in cystic fibrosis (CF), lung function has also steadily improved. Forced expiratory volume in one second (FEV 1), the measure of airway obstruction most widely monitored in patients with CF, often does not fall below the normal range until late adolescence. Clearly, FEV1 is losing relevance for clinicians monitoring lung disease in children with CF, as it is frequently normal, declines slowly, and cannot be measured by conventional techniques in children <6 years of age. As clinicians increasingly aim to identify and treat early CF lung disease before irreversible structural airway damage occurs, there is a compelling need for better tools with which to monitor for early lung structural and physiologic abnormalities in our youngest CF patients. Three promising measures are infant and preschool lung function testing, chest computed tomography, and multiple breath washout measures of the lung clearance index. The current state of these tests as they relate to the clinical monitoring of early CF lung disease is reviewed, and improvements on the horizon that may allow them to be adopted in clinical practice explained.

Original languageEnglish (US)
Pages (from-to)133-137
Number of pages5
JournalPediatric, Allergy, Immunology, and Pulmonology
Issue number3
StatePublished - Sep 1 2011
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Immunology and Allergy
  • Pulmonary and Respiratory Medicine

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