Journal of Cystic Fibrosis
Volume 9, Issue 2 , Pages 130-134, March 2010

Upper and lower airway cultures in children with cystic fibrosis: Do not neglect the upper airways

Department of Paediatric Respiratory Disease, Cystic Fibrosis Centre Utrecht, Wilhelmina Children's Hospital, KH 01.419.0, University Medical Centre Utrecht, P.O. Box 85090, 3508 AB Utrecht, The Netherlands

Received 5 October 2009; received in revised form 23 December 2009; accepted 4 January 2010.

Abstract 

Background

Airways of cystic fibrosis (CF) patients are colonised with bacteria early in life. We aimed to analyse differences between results of simultaneously taken upper airway (UAW) and lower airway (LAW) cultures, to describe clinical characteristics of patients with positive versus negative cultures and to follow up the patients with P. aeruginosa positive UAW cultures.

Methods

Bacteriological and clinical data from 157 children were collected during annual check up. The number of positive UAW and LAW cultures and correspondence between these results and clinical characteristics were analysed.

Results

Positive LAW and UAW cultures were found in 79.6% and 43.9% of patients respectively (p<0.001). Patients with positive LAW cultures were significantly older (11.9 vs. 9.8years, p<0.05) and had more LAW symptoms (73.6% vs. 46.7%, p<0.05), especially when P. aeruginosa was found. Patients with positive UAW cultures (especially S. aureus) had more nasal discharge (50.7% vs. 25.0%, p<0.001). In 65% of patients with positive UAW and negative LAW culture for P. aeruginosa the next LAW became P. aeruginosa positive.

Conclusion

UAW cultures and LAW cultures differ in children with CF and there are differences in clinical characteristics between patients with positive versus negative culture results. P. aeruginosa positive UAW cultures appeared to precede positive LAW cultures in a substantial part of patients, suggesting some kind of cross-infection between the UAW and LAW.

Keywords: Bacterial colonisation, Cystic fibrosis, Lower airways, Pseudomonas aeruginosa, Upper airways

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PII: S1569-1993(10)00005-6

doi:10.1016/j.jcf.2010.01.001

Journal of Cystic Fibrosis
Volume 9, Issue 2 , Pages 130-134, March 2010