Subject characteristics (n=62)
Cystic fibrosis (CF) (n=46) | Controls (n=16) | p Value | |
Sex, F:M | 27:19 | 10:6 | 0.789 |
Age, years | 7.8 (0.2–16.8) | 6.3 (0.2–16.4) | 0.334 |
FEV1, % predicted* | 53 (29–84) | 98 (61–131) | 0.001 |
FVC, % predicted* | 74 (32–99) | 93 (85–137) | 0.006 |
CFTR genotype (n, %) | F508del/F508del (n=27, 59%); F508del/G542X (n=2, 4%); F508del/1717-1G>A (n=2, 4%); F508del/other (n=6, 13%); other or unknown (n=9, 20%). | ND | ND |
Indication for bronchoscopy (n) |
|
| ND |
Pathogens in BAL fluid | No virus detection, no bacterial growth | ND |
Values expressed as median (range) unless otherwise indicated.
↵* Data available for 29 children with CF and six control children.
↵† Chest exacerbation based on the decision to hospitalise and treat with intravenous antibiotics.26
↵‡ Staphylococcus aureus (n=2), Haemophilus influenzae (n=1), Mycobacterium chelonae (n=2), Stenotrophomonas maltophilia (n=1).
↵§ Aspergillus fumigatus (n=12), Aspergillus niger (n=1).
BAL, bronchoalveolar lavage; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; ND, not determined.