Study group characteristics
Bronchiectasis(n = 44) | Cystic fibrosis(n = 44) | |
---|---|---|
BMT, bone marrow transplant. | ||
*⩾1 occasion over study period. | ||
†Non-typeable, ⩾3 positive cultures in 1 year. | ||
‡25 (59%) of those with CF were prescribed inhaled corticosteroids. | ||
Spirometric studies (median per individual) | 931 (15) | 2066 (45) |
Mean calendar years of data | 4.7 years | 6.7 years |
Lung volume studies (median per individual) | 368 (7) | 621 (13) |
Mean (range) age at testing(all studies), years | 10.7 (5–15) | 10.1 (5–15) |
Sex: % female | 57% | 48% |
Ethnicity, n (%) | ||
Maori | 12 (27%) | 2 (5%) |
European | 7 (16%) | 40 (91%) |
Pacific | 25 (57%) | 0 (0%) |
Other | 0 (0%) | 2 (5%) |
BX aetiology | ||
Unknown | 22 (50%) | |
Post-infectious | 7 (16%): 6 due to adenovirus,1 to B pertussis | |
Primary immunodeficiency | 6 (14%): 5 humoral, 1 combined deficiencies | |
“Post-oncology disease/Rx” | 6 (14%): 4 leukaemia (2 BMT),2 lymphoma | |
Other | 3 (7%) | |
Asthma diagnosis | 17 (39%) | 5 (11%)‡ |
β2 agonist response >12%*19 | 21 (48%) | 31 (70%) |
Median (range) CT score | 24 (4–65) | |
Laterality of disease | 89% bilateral | |
Median diseased lobes | 4 (5% unilobular) | |
Chronic Haemophilus influenza infection†9 | 18 (41%) | |
Chronic Pseudomonas infection | 0 (0%) | 24 (55%) |
Median age at diagnosis (initiation of specific treatment) | 7.5 years | 1 month |