An assessment of sinus quality of life and pulmonary function in children with cystic fibrosis. Academic Article uri icon

Overview

abstract

  • BACKGROUND: Treatment of patents with cystic fibrosis (CF) is primarily directed at the lungs. However, there is a growing feeling that the status of the sinuses may have a profound influence on the status of the lungs in these patients. A number of investigators have demonstrated a relationship among coexisting rhinitis, sinusitis, other upper airway conditions, and lung disease. Several studies have shown that treatment and resolution of sinusitis results in an improvement in a number of pulmonary conditions. We hypothesize that pulmonary function test scores will be lower in patients with CF with more severe sinusitis. METHODS: Consecutive CF patients were asked to complete a sinus-specific quality-of-life instrument, the 16-item Sino-Nasal Outcome Test (SNOT-16), and these scores, were compared to FEV, scores. RESULTS: Univariate analysis revealed a significant correlation between SNOT-16 and FEV1 in patients under the age of 12. There was a trend toward significance in the older children and evaluation of the raw data shows that children with the highest FEV, had the lowest SNOT-16. CONCLUSION: This study indicates that the severity of sinus disease correlates with the severity of pulmonary disease in CF patients under the age of 12. We plan to use the SNOT-16 to assess sinus interventions on pulmonary status.

publication date

  • January 1, 2006

Research

keywords

  • Cystic Fibrosis
  • Forced Expiratory Volume
  • Quality of Life
  • Sinusitis

Identity

Scopus Document Identifier

  • 33845685873

Digital Object Identifier (DOI)

  • 10.2500/ajr.2006.20.2915

PubMed ID

  • 17181094

Additional Document Info

volume

  • 20

issue

  • 6