scholarly journals Congenital duodenal obstruction: timing of diagnosis during the newborn period

2009 ◽  
Vol 30 (3) ◽  
pp. 197-200 ◽  
Author(s):  
H Kilbride ◽  
C Castor ◽  
W Andrews
Keyword(s):  
Duodenal Obstruction ◽  
Newborn Period ◽  
Congenital Duodenal Obstruction

CONGENITAL ATRESIA AND STENOSIS OF THE DUODENUM

PEDIATRICS ◽  
1969 ◽  
Vol 43 (1) ◽  
pp. 79-83
Author(s):  
Eric W. Fonkalsrud ◽  
Alfred A. deLorimier ◽  
Daniel M. Hays
Keyword(s):  
Congenital Malformations ◽  
Duodenal Obstruction ◽  
Duodenal Atresia ◽  
Operative Techniques ◽  
Congenital Atresia ◽  
Late Mortality ◽  
Congenital Duodenal Obstruction ◽  
American Academy Of Pediatrics ◽  
Associated Malformations ◽  
Major Congenital Malformations

A review is presented of 503 patients with congenital duodenal obstruction, compiled from 65 hospitals by the Surgical Section of the American Academy of Pediatrics. Four hundred eighty-seven patients underwent primary operative correction of the malformation with an overall early and late mortality rate of 36%. Complications from associated major congenital malformations were the leading cause of death. Many of these anomalies were potentially correctable had they been recognized and early treatment instituted. More than half of the infants with duodenal atresia had associated malformations. Thirty percent of the patients had Down's syndrome. End-to-side or side-to-side duodenoduodenostomy or jejunostomy are the most commonly used operative techniques for duodenal atresia. General anesthesia and tube gastrostomy are usually employed.

scholarly journals Clinical Study of Congenital Duodenal Obstruction

1998 ◽  
Vol 15 (1) ◽  
pp. 67
Author(s):  
Young Soo Huh ◽  
Myeung Kook Lim ◽  
Sung Kyu Park
Keyword(s):  
Clinical Study ◽  
Duodenal Obstruction ◽  
Congenital Duodenal Obstruction

Congenital Duodenal Obstruction and Mongolism

BMJ ◽  
1952 ◽  
Vol 1 (4754) ◽  
pp. 384-385
Author(s):  
V. Smallpeice ◽  
M. Coxon
Keyword(s):  
Duodenal Obstruction ◽  
Congenital Duodenal Obstruction

Congenital Duodenal Obstruction: An Approach to Diagnosis

1993 ◽  
Vol 3 (05) ◽  
pp. 267-270 ◽  
Author(s):  
S. Eustace ◽  
B. Connolly ◽  
N. Blake
Keyword(s):  
Duodenal Obstruction ◽  
Congenital Duodenal Obstruction

Congenital Duodenal Obstruction: Evaluation of 68 Cases

2021 ◽  
Author(s):  
Emel Çolak ◽  
Ayşenur Celayir
Keyword(s):  
Duodenal Obstruction ◽  
Associated Anomalies ◽  
Hospital Records ◽  
Cardiac Malformations ◽  
Congenital Duodenal Obstruction ◽  
Clinical Presentations ◽  
Hospitalization Period ◽  
Common Causes ◽  
The Mean ◽  
Associated Abnormalities

INTRODUCTION: Congenital duodenal obstruction, which is one of the most common causes of intestinal obstruction in neonates, gain importance in terms of associated anomalies. In this study, we aimed to review our experience with congenital duodenal obstruction cases operated in our clinic while evaluating the results of these patients. METHODS: All hospital records of neonates with congenital duodenal obstruction which had operated in our department between 2004 and 2017 were reviewed retrospectively. Patients were evaluated according to their demographic features, clinical presentations, associated anomalies, treatments and outcomes. RESULTS: During 13 years, 68 newborns (36 males, 32 females) with congenital duodenal obstruction were operated. The mean gestational age was 35.7±3.1weeks (28-44weeks), the mean birth weight was 2477±651.5 gram (1100–4100 gram) and 46 (67.7%) of them were premature. Associated abnormalities were detected in 37 neonates (54.4%); 16 of them (23.5%) had congenital cardiac malformations, and 13 of them (19.1%) had Down Syndrome. In neonates with associated abnormalities; the avarage period to start enteral feeding was 9.5±5.8 days (4-37days) and the mean hospitalization period was 25.6±26.2days (9-140days). These values were found 7.6±3.2 days (4-20days) and 17.5±13.7days (8-80days) respectively for the patients having no associated anomalies. Postoperative complications such as ileus, septicemia and nutritional intolerance were seen in 17 patients (25%); 3 of them (4.4%) need re-operation. While 63 patients (92.6%) were discharged on average 21.4±22 days (8-140 days); due to septicemia and severe congenital cardiac malformations 5 patients (7.4%) were died in 27.2±14.1 days (11-43days) postoperatively. The rate of septicemia was statistically significantly higher in patients with excitus than the ones who were discharged (p<0.001). DISCUSSION AND CONCLUSION: The presence of associated abnormalities in patients with congenital duodenal obstruction increases the risk of morbidity and mortality. Septicemia and severe congenital cardiac malformations adversely affect prognosis.

scholarly journals Concurrence of Hirschsprung Disease and congenital duodenal obstruction

2020 ◽  
Vol 61 ◽  
pp. 101585
Author(s):  
Fatima Bawany ◽  
Ankit Patel ◽  
Christopher Gitzelmann ◽  
Derek Wakeman
Keyword(s):  
Duodenal Obstruction ◽  
Hirschsprung Disease ◽  
Congenital Duodenal Obstruction
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