Affiliation:
1. Departments of Otolaryngology and The Hospital for Sick Children, Toronto, Canada
2. Departments of Respiratory Medicine, The Hospital for Sick Children, Toronto, Canada
Abstract
Clinical assessments and rhinomanometric evaluations were performed in 143 consecutive cystic fibrosis (CF) patients ranging in age from 4 to 40 years (mean, 18.8). Nasal stuffiness, the most common symptom, correlated strongly with polyposis; however, nasal airflow resistance (NR) was not correlated with the incidence of polyps. Diminished NR was found in many CF patients, in 57 of them NR was < 1.0 cm H2O/L/sec (Pa/cm3/sec × 10), and was associated with impaired pulmonary function (p = 0.001).
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