Abstract
Multiple breath washout (MBW) measurements have recently been shown to be sensitive for detection of early cystic fibrosis (CF) lung disease, with the lung clearance index (LCI) being the most common measure for ventilation inhomogeneity. The aim of this observational study was to describe the longitudinal course of LCI from time of clinical diagnosis during infancy to school-age in eleven children with CF. Elevated LCI during infancy was present in seven subjects, especially in those with later clinical diagnosis. Tracking of LCI at follow-up was evident only in the four most severe cases. We provide the first longitudinal data describing the long-term course of LCI in a small group of infants with CF. Our findings support the clinical usefulness of MBW measurements to detect and monitor early lung disease in children with CF already present shortly after clinical diagnosis.
| Original language | English |
|---|---|
| Journal | Journal of Cystic Fibrosis |
| Volume | 10 |
| Issue number | 6 |
| Pages (from-to) | 487-490 |
| Number of pages | 4 |
| ISSN | 1569-1993 |
| DOIs | |
| Publication status | Published - 12.2011 |
Funding
Supported by the Swiss Confederation's Innovation Promotion Agency (CTI) grant no. 11661.1 PFLS-LS and the “Fondazione Ettore e Valeria Rossi”.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Areas and Centers
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)
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