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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: J Pediatr. 2016 Oct 25;180:206–211.e1. doi: 10.1016/j.jpeds.2016.09.069

Table 2.

Description of neonatal adverse outcomes for a cohort of children with cystic fibrosis (CF present) compared to birth-year matched children without CF (CF absent) in Washington State from 1996- 2013 and 2006-20131

1996-2013 2006-2013

CF Present (N=170) CF Absent (N=3400) CF Present (N=68) CF Absent (N=1360)

Low Birth Weight (<2500 grams), n (%) 32 (18.8) 201 (5.9) 17 (25.0) 92 (6.8)
Small for Gestational Age2 (<10th percentile), n (%) 23 (13.5) 286 (8.4) 5 (7.4) 109 (8.0)
Pre-term Birth (<37 weeks), n (%) 41 (24.1) 288 (8.5) 19 (27.9) 140 (10.3)
Infant Death3 (Death <1 year), n (%) 3 (1.8) 11 (0.3) 3 (4.4) 5 (0.4)
1

<1% missing data unless otherwise noted

2

SGA missing for 1.2% of children with CF present (1996-2013), and for 3.8% of children with CF absent (1996-2013); SGA missing for 2.9% of children with CF present (2006-2013), and for 2.9% of children with CF absent (2006-2013)

3

Infant death among infants with CF present occurred in 2 infants without meconium ileus and 1 infant with meconium ileus

CF=cystic fibrosis, SGA=small for gestational age