Case Control Study
Copyright ©The Author(s) 2019.
World J Gastroenterol. Jul 28, 2019; 25(28): 3787-3797
Published online Jul 28, 2019. doi: 10.3748/wjg.v25.i28.3787
Table 1 Demographic data for 50 patients with complete or incomplete congenital duodenal obstruction undergoing operative repair
CompleteIncompleteP value
n = 27n = 23
Gender (male:female), n (%)12 (44):15 (56)12 (52):11 (48)0.78
Gestational age at birth (wk)36.0 (31.3-42)38.7 (30.1-40.1)0.01a
No CHD + GA ≥ 37 wk (wk)38.6 (38.3-39.0), n = 439.3 (37.1-40.1), n = 150.34
GA < 37 wks (patients), n (%)14 (52)5 (22)< 0.05a
Age at operation, AO (d)1.0 (0-7)21.0 (3-2790)< 0.01a
No CHD + GA ≥ 37 wk (d)1.0 (0-7), n = 421.0 (3-2790), n = 15< 0.01a
Weight at operation (kg)2.54 (1.48-3.84)3.27 (2.20-13.80)< 0.01a
No CHD + GA ≥ 37 wk (kg)3.20 (2.98-3.45), n = 43.92 (2.48-12.80), n = 150.37
Associated congenital anomalies (patients), n (%)20 (74)7 (30)< 0.01a
Congenital heart disease (patients), n (%)18 (67)3 (13)< 0.01a
Trisomy 21 (patients), n (%)11 (41)4 (17)0.12
Other anomalies (patients), n (%)10 (37)6 (26)0.55
DetailsButterfly vertebrae (1), esophageal atresia (1), hemolytic disease of the newborn (1), hydronephrosis, unilateral (1), bilateral (1), hypothyreosis (5), funnel trachea (1), polydactyly, unilateral (1), Hirschsprung disease (1), atopic eczema (1)Pes calcaneus (1), biliary duct hypoplasia (1), celiac disease (1), Cornelia de Lange syndrom (1), sleep apnoea (1), ectrodactyly, bilateral (1), hypospadia (1), patent omphalomesenteric duct (1), glutaric aciduria type 1 (1)