Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis.

@article{Harrison2009LongitudinalAO,
  title={Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis.},
  author={Amy Harrison and Warren E. Regelmann and Jacquelyn M Zirbes and Carlos E Milla},
  journal={Pediatric pulmonology},
  year={2009},
  volume={44 4},
  pages={330-9}
}
RATIONALE Infant pulmonary function testing (IPFT) has become an important clinical tool for the evaluation of lung function in infants with Cystic Fibrosis (CF); however, it is still unclear whether lung function in infancy is predictive of lung function later in life. We hypothesized that measures of airflow obstruction by IPFT would correlate strongly with lung function by conventional spirometry later in childhood. STUDY DESIGN AND METHODOLOGY A retrospective analysis was performed of all… CONTINUE READING
13 Citations
38 References
Similar Papers

Citations

Publications citing this paper.
Showing 1-10 of 13 extracted citations

References

Publications referenced by this paper.
Showing 1-10 of 38 references

Longitudinal analysis of pulmonary function in cystic fibrosis infants

  • AN Harrison, WE Regelmann, CM. Milla
  • Pediatr Pulmonol 2006;41:A367
  • 2006
Highly Influential
3 Excerpts

Lung function from infancy to age 6y in screened CF children: hyperinflation but not airway flow obstruction (ao) is an early marker of CF lung disease

  • I Michelet, L Couderc, C Leguillon, B. Masseline
  • Pediatr Pulmonol 2007;S30:A387
  • 2007
2 Excerpts

Respiratory mechanics

  • SD Davis, M Gappa, M. Rosenfeld
  • 2005

Similar Papers

Loading similar papers…