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. 2019 Dec 9;39(6):740–756. doi: 10.1002/sim.8443

Table 1.

Clinical and demographic composition of the cystic fibrosis data

Characteristics Development cohort (n = 24 704) Validation cohort (n = 6175)
Birth cohort
<1981 5455 (22.1%) 1336 (21.6%)
1981 to 1988 4886 (19.8%) 1220 (19.8%)
1989 to 1994 4476 (18.1%) 1090 (17.7%)
1995 to 1998 2887 (11.7%) 727 (11.8%)
1999 to 2005 4642 (18.8%) 1170 (18.9%)
>2005 2358 (9.5%) 632 (10.2%)
Genotype (F508del mutation type)
Homozygous 11 150 (45.1%) 2851 (46.2%)
Heterozygous 9884 (40%) 2430 (39.4%)
Neither/unknown 3670 (14.9%) 894 (14.5%)
Male gender 12 744 (51.6%) 3211 (52%)
Age at baseline, mean; median (min‐max) 16.6; 12.5 (6.0‐81.8) 16.5; 12.4 (6.0‐79.0)
FEV1 at baseline mean; median (min‐max) 79.8; 83.8 (9.3‐149.3) 80.1; 82.9 (8.8‐143.4)
Medicaid insurance use
At baseline 11 069 (44.8%) 2759 (44.7%)
Ever during follow‐up 19 032 (77%) 4789 (77.6%)
Microbiology
Pseudomonas aeruginosa
At baseline 6509 (26.3%) 1646 (26.7%)
Ever during follow‐up 18 434 (74.6%) 4649 (75.3%)
Methicillin‐resistant Staphylococcus aureus
At baseline 1774 (7.2%) 472 (7.6%)
Ever during follow‐up 10 821 (43.8%) 2639 (42.7%)
CF‐related diabetes mellitus
At baseline 1961 (7.9%) 490 (7.9%)
Ever during follow‐up 7525 (30.5%) 1853 (30%)
Alive through follow‐up 23 692 (95.9%) 5927 (96%)

Abbreviations: CF, cystic fibrosis; FEV1, forced expiratory volume in 1 second of percentage of predicted.