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. Author manuscript; available in PMC: 2017 Feb 21.
Published in final edited form as: Pediatr Pulmonol. 2016 Aug 24;51(11):1168–1176. doi: 10.1002/ppul.23536

TABLE 2.

Clinical Characteristics of CF Infants (N = 43)

Variable Mean (SD) or %
Genotype (F508del homozygous) 56%
CFTR function (mean sweat chloride, mmol/L) 98 (13.1)
iPFT
  FVC% 108 (17.2)
  FEV0.5% 102 (19.9)
  FEF25–75% 96 (28.5)
  RV/TLC% 144 (24.6)
Nutritional status (weight/length percentile
  at 12 months)
65% (24%)
Microbiology (history of PsA) 44%
Cough (occasional/daily) 42%
Pulmonary exacerbations (in first 12 months
  of life; range 1–5)
1.9 (1.5)
Hospitalizations (in first 12 months of life) 47%
Clinical score (range 0–10) 7.6 (2.1)
Prescribed chronic pulmonary therapies 67%
  Inhaled corticosteroid 42%
  Dornase alpha 40%
  Azithromycin 23%