Lower Lung Function and Bronchiectasis in Cystic Fibrosis Increases the Risk of Obstructive Sleep Apne

  • Castro-Elias W
  • Hopkins B
  • Smith E
N/ACitations
Citations of this article
6Readers
Mendeley users who have this article in their library.
Get full text

Abstract

PURPOSE: To determine if cystic fibrosis (CF) patients with severe obstructive lung disease have a higher prevalence of obstructive sleep apnea (OSA). METHODS: Charts of 25 hospitalized pediatric CF patients were reviewed. Chest x-ray/CT scan to determine presence of bronchiectasis and spirometry to determine the lowest lung function during the past year. Degree of severity was based on forced expiratory volume in 1 second (FEV 1) from the ATS/ERS task force standardization of lung function testing. Patients were divided into 2 groups as follows: mild and moderate (level I) vs. moderate-severe, severe, very severe (level II). Level I severity was a FEV1 greater than or equal to 60% predicted and level II was less than or equal to 59% predicted. The hospitalized CF patients were screened for OSA with the Pediatric Sleep Questionnaire. ItaTMs a validated questionnaire with a sensitivity of 0.85 and a specificity of 0.87 when 8 or more answers of the 22 question-items are abnormal. The relationship between lung function and OSA was assessed using contingency table analysis (Fisher's exact test). RESULTS: 12 patients (48%) screened positive for OSA. 21 patients (84%) had bronchiectasis. 15 patients (60%) had level II lung function. No statistically significant association was found between lung function severity level and OSA. 40% of level I patients with OSA compared to 53.3% of level II patients (p=0.688). When stratified for bronchiectasis (Yes or No), among those with bronchiectasis, 0% of severity level I patients compared to 53.3% of level II patients had OSA (low-bias estimate of relative risk 3.733, 95% CI 0.164-0.902, p=0.046). CONCLUSIONS: This study indicates that the prevalence of OSA is higher in hospitalized pediatric CF patients (48%) compared to the general pediatric population (0.7-10.3%). The CF patients with bronchiectasis have a significant association between lung function severity level and OSA. There is a higher percentage of OSA in the severely obstructed group (level II).

Cite

CITATION STYLE

APA

Castro-Elias, W., Hopkins, B., & Smith, E. O. (2012). Lower Lung Function and Bronchiectasis in Cystic Fibrosis Increases the Risk of Obstructive Sleep Apne. Chest, 142(4), 766A. https://doi.org/10.1378/chest.1390356

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free