TABLE 2 Cox proportional hazard models for death in the contemporary cystic fibrosis (CF) cohort: 2000–2012
UnivariateMultivariate
Sex
 MaleRef.Ref.
 Female1.35 (1.12–1.61)1.28 (1.00–1.63)
Genotype
 OtherRef.
 Homozygous ΔF5081.54 (1.08–2.21)
 Heterozygous ΔF5081.20 (0.84–1.73)
 Missing3.01 (1.89–4.81)
Pancreatic insufficiency
 SufficientRef.Ref.
 Insufficient3.18 (2.19–4.61)2.19 (1.15–4.17)
Age at diagnosis
<2 yearsRef.Ref.
 2–18 years0.62 (0.50–0.77)0.79 (0.59–1.06)
 >18 years0.30 (0.20–0.44)0.55 (0.28–1.11)
Longest time in a region
 QuebecRef.
 East1.53 (1.13–2.09)
 Ontario1.01 (0.81–1.28)
 West1.27 (1.00–1.61)
Exacerbations per year
 0Ref.Ref.
 1–26.17 (3.69–10.31)2.98 (2.14–4.15)
 ≥311.12 (5.58–21.78)4.53 (3.19–6.43)
CF-related diabetes2.26 (1.36–3.78)
Microbiology#
Burkholderia cepacia complex2.51 (1.40–4.50)1.89 (1.44–2.49)
Staphylococcus aureus0.32 (0.19–0.53)
Pseudomonas aeruginosa2.05 (0.98–4.27)
Stenotrophomonas maltophilia1.17 (0.73–1.86)0.75 (0.58–0.97)
 MRSA0.70 (0.25–1.94)
BMI categories
 Adequate weightRef.Ref.
 Overweight0.22 (0.06–0.80)0.80 (0.47–1.35)
 Underweight12.44 (6.26–24.75)2.12 (1.60–2.82)
FEV1% predicted0.91 (0.89–0.93)0.95 (0.94–0.96)
Birth year0.96 (0.93–0.99)
  • Data are presented as hazard ratio (95% CI). MRSA: methicillin-resistant S. aureus; BMI: body mass index; FEV1: forced expiratory volume in 1 s. #: reference group for each bacterium was individuals who were culture negative for that bacterium.