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. Author manuscript; available in PMC: 2016 Feb 2.
Published in final edited form as: Arch Dis Child Fetal Neonatal Ed. 2010 Aug 5;96(2):F114–F120. doi: 10.1136/adc.2010.182865

Table 3.

Univariate associations between late neonatal factors and the risk of chronic lung disease (CLD). The right-most column provides the maximum number of infants with the attribute listed in each row; any differences are due to missing data. All other data are the percentage of infants with CLD among those infants with the attribute listed on the two left columns and the respiratory patterns listed as column headings. For example, among infants who received hydrocortisone that had the Low FiO2 respiratory pattern, the prevalence of CLD was 40%.

Late neonatal factors Respiratory Pattern Row
N
Low FiO2 PD* EPPD*
Hydrocortisone Yes 40 76 69 142
No 17 40 69 1062
Dexamethasone Yes 50 74 86 78
No 17 51 67 1126
Analgesic Yes 27 66 75 578
No 14 39 60 626
Sedation Yes 32 63 74 264
No 16 49 67 940
Vitamin A Yes 21 50 65 354
No 16 52 72 850
Confirmed
bacteremia
Yes 16 63 73 298
No 17 48 68 905
Confirmed tracheal
infection
Yes 28 63 74 230
No 17 49 68 964
Mechanical
ventilation(day 14)**
Yes 31 72 77 717
No 14 26 36 486
Mechanical
ventilation(day 21)**
Yes 43 72 77 696
No 12 27 39 504
Patent ductus
arteriosus (PDA)
Yes 20 58 71 798
No 14 40 64 406
Pneumothorax
(PTX)
Yes 25 73 81 91
No 17 50 68 1113
Pulmonary interstitial
emphysema (PIE)
Yes 50 79 85 189
No 16 49 63 1015
Necrotizing
Enterocolitis***
No/Stage I, II 15 50 69 1009
Stage IIIa 100 67 50 13
Stage IIIb 38 92 68 48
Isolated perf 50 71 88 34
Percent CLD 17 52 69 52
Maximum Column N 240 456 508 1204
*

PD=pulmonary deterioration, EPPD=early and persistent pulmonary dysfunction

**

Includes conventional mechanical ventilation and high frequency ventilation

***

Bell's staging