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. 1998 Jun 13;316(7147):1771–1775. doi: 10.1136/bmj.316.7147.1771

Table 1.

Characteristics of three groups of cystic fibrosis patients* (P value represents any difference between the three groups)

Variable Group A (n=50) Group B (n=47) Group C (n=36) P value
Mean and SD of age (years) 22.9 (4.49)   27.5 (7.50)   25.0 (6.42)   0.002
Median and interquartile range of age at time of diagnosis (months) 6.0 (22.0)  15.0 (81.0)   12.0 (34.5)   0.088
Sex (%):
 Male 28 (56.0) 23 (48.9) 26 (72.2) 0.097
 Female 22 (44.0) 24 (51.1) 10 (27.8)
Cystic fibrosis genotype (%)§:
 508/508 32 (63.3) 25 (55.5) 17 (56.7) 0.199
 508/Other 12 (26.5) 19 (42.2)  9 (30.0)
 Non-508/non-508  5 (10.2) 1 (2.2)  4 (13.3)
Liver disease (%):
 Not present 43 (86.0) 41 (87.2) 30 (83.3) 0.879
 Present  7 (14.0)  6 (12.8)  6 (16.7)
Pancreatic status (%):
 Insufficient 48 (96.0) 40 (85.1) 35 (97.2) 0.057
 Sufficient 2 (4.0)  7 (14.9) 1 (2.8)
Diabetes mellitus (%):
 Not present 39 (78.0) 38 (80.9) 27 (75.0) 0.814
 Present 11 (22.0)  9 (19.1)  9 (25.0)
Pseudomonas aeruginosa (%):
 Not colonised  5 (10.0)  5 (10.6) 10 (27.8) 0.043
 Colonised 45 (90.0) 42 (89.4) 26 (72.2)
Burkholderia cepacia (%):
 Not colonised 31 (62.0) 39 (83.0) 32 (88.9) 0.007
 Colonised 19 (38.0)  8 (17.0)  4 (11.1)
Smoking status (%):
 Non-smoker 43 (86.0) 45 (95.7) 33 (91.7) 0.243
 Current or ex-smoker  7 (14.0) 2 (4.3) 3 (8.3)
α1 Antitrypsin phenotype (%):
 Normal 42 (85.7) 39 (83.0) 29 (85.3) 0.926
 Deficient  7 (14.3)  8 (17.0) 5 (14.7)
*

Group A patients had had both paediatric and adult care in a cystic fibrosis centre; group B patients had not had paediatric but had had adult care in a cystic fibrosis centre; group C patients had had no care in a cystic fibrosis centre. One way analysis of variance. Kruskal-Wallis test. §Not available for one, two, and six patients in groups A, B, and C respectively. χ2 test.