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. 2019 Jan 3;35(2):197–204. doi: 10.1007/s12291-018-0807-1

Table 3.

Secondary outcomes (respiratory and non-respiratory)

Parameter Vitamin A group (n = 55) Placebo group (n = 59) p value
Duration of any ventilation (h) n = 20 n = 21 0.39
Median (1st–3rd quartile) 96 (72,120) 120 (72,168)
Duration of invasive ventilation (h) n = 14 n = 8 0.07
Median (1st–3rd quartile) 72 (66,102) 108 (96,138)
Duration of oxygen therapy (h) n = 35 n = 29 0.22
Median (1st–3rd quartile) 120 (72,216) 144 (96,282)
Infants requiring oxygen at end of the study n (%) 8 (13) 11 (19) 0.41
Infants requiring invasive ventilation at the end of the study n (%) 0 (0) 4 (7) 0.055a
BPD n (%) 5 (8) 7 (12) 0.55
Severity of BPD n (%) 0.23a
 Mild 4 (80) 3 (42)
 Moderate 1 (20) 2 (29)
 Severe 0 2 (29)
Duration of hospitalization (days) 31 (18, 43) 27 (20, 46) 0.71
Median (1st–3rd quartile)
Intraventricular hemorrhage n (%) 5 (8) 6 (10) 0.71
All-cause mortality n (%) 8 (13) 4 (7) 0.36
Periventricular leukomalacia n (%) 2 (3.3) 4 (6.8) 0.43a
Blood stream infection n (%) 22 (36) 18 (30) 0.52
Pneumonia n (%) 18 (30) 20 (34) 0.60

Analysis of all categorical variables was by Chi square and all numerical variables was by Mann–Whitney test unless specified

BPD, bronchopulmonary dysplasia

aFisher’s exact test