Otolaryngological and Rhinomanometric Findings in Cystic Fibrosis

Author:

Leiberman Alberto1,Cole Philip1,Corey Mary2,Forte Vito1,Levison Henry2

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).

Publisher

SAGE Publications

Subject

Otorhinolaryngology

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cystic Fibrosis: Brazilian ENT Experience;International Journal of Otolaryngology;2012

2. Nasal endoscopic evaluation of children and adolescents with cystic fibrosis;Brazilian Journal of Otorhinolaryngology;2009-11

3. Cystic Fibrosis: An Update for the Otolaryngologist;Otolaryngology–Head and Neck Surgery;1999-04

4. Inflammatory Cells and Mediator Concentrations in Nasal Secretions of Patients with Cystic Fibrosis;Acta Oto-Laryngologica;1996-01

5. Pathological changes of the lateral nasal wall in patients with cystic fibrosis (mucoviscidosis);International Journal of Pediatric Otorhinolaryngology;1994-01

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