Congenital Duodenal Obstruction: Evaluation of 68 Cases

Q4 Medicine
Emel Colak, A. Celayir
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引用次数: 0

Abstract

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.
先天性十二指肠梗阻68例分析
简介:先天性十二指肠梗阻是新生儿肠梗阻最常见的原因之一,在相关异常方面受到重视。在这项研究中,我们的目的是回顾我们的经验,先天性十二指肠梗阻的情况下,在我们的诊所进行手术,并评估这些患者的结果。方法:回顾性分析2004 ~ 2017年在我科手术治疗的先天性十二指肠梗阻新生儿的住院记录。根据患者的人口学特征、临床表现、相关异常、治疗和结果对患者进行评估。结果:13年来共收治新生儿先天性十二指肠梗阻68例(男36例,女32例)。平均胎龄为35.7±3.1周(28 ~ 44周),平均出生体重为2477±651.5克(1100 ~ 4100克),早产46例(67.7%)。相关异常37例(54.4%);其中先天性心脏畸形16例(23.5%),唐氏综合征13例(19.1%)。伴有相关异常的新生儿;平均开始肠内喂养时间为9.5±5.8天(4 ~ 37天),平均住院时间为25.6±26.2天(9 ~ 140天)。无相关异常的患者分别为7.6±3.2天(4 ~ 20天)和17.5±13.7天(8 ~ 80天)。术后并发症如肠梗阻、败血症和营养不耐受17例(25%);其中3例(4.4%)需再次手术。63例(92.6%)平均出院21.4±22天(8 ~ 140天);因败血症及严重先天性心脏畸形死亡5例(7.4%),死亡时间为术后27.2±14.1天(11 ~ 43天)。兴奋期患者败血症发生率明显高于出院期患者(p<0.001)。讨论与结论:先天性十二指肠梗阻患者的相关异常增加了发病率和死亡率的风险。败血症和严重的先天性心脏畸形对预后有不利影响。
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来源期刊
Cocuk Cerrahisi Dergisi
Cocuk Cerrahisi Dergisi Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.10
自引率
0.00%
发文量
21
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