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首页> 外文期刊>Journal of pediatric gastroenterology and nutrition >Clinical and nutritional outcomes in children with idiopathic superior mesenteric artery syndrome.
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Clinical and nutritional outcomes in children with idiopathic superior mesenteric artery syndrome.

机译:儿童特发性肠系膜上动脉综合征的临床和营养结果。

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摘要

OBJECTIVE: There are no available data for outcomes in children's idiopathic superior mesenteric artery syndrome (SMAS) strictly treated conservatively. The aim of the study was to evaluate clinical and nutritional outcome in children with idiopathic SMAS. PATIENTS AND METHODS: A 1-year prospective observation study of effects of treatment and outcome was performed in 27 children (8 boys, 19 girls) with idiopathic SMAS who underwent an upper gastrointestinal (UGI) series, ultrasound measurement of the aortomesenteric angle, treatment, clinical assessment, growth evaluation, and regular clinical visits for more than 12 months. RESULTS: Mean age of the patients was 11.77 +/- 2.15 years. The major clinical complaints were postprandial pain or fullness (88.9%), vomiting (55.6%), and early satiety (51.9%). Eight patients (29.6%) had weight loss. The UGI series revealed typical features of SMAS. The aortomesenteric angle on ultrasound was 10 degrees to 19 degrees. The height of most patients (92.6%) was above the 10th percentile, whereas 15 (55.6%) patients weighed below the 10th percentile. Six patients underwent surgical intervention (3 for obstruction and 3 for persistent anorexia with weight loss), and their clinical symptoms and weight status improved steadily during the follow-up months. Among the 21 patients not subject to surgical intervention, 11 (52.4%) experienced a reduction of symptoms >50% after 3 months of treatment, and weight-for-age percentile increased significantly after 6 months of treatment. Overall, a significant increase in the weight-for-age status was seen in the patients with surgical treatment or with medication only after 6 and 12 months of treatment. CONCLUSIONS: An aortomesenteric angle <20 degrees is a constant phenomenon in children with idiopathic SMAS. A duodenojejunostomy can effectively relieve the obstructive symptoms, such as anorexia, and improve nutritional status, whereas long-term medical treatment may aid in relieving the clinical symptoms, promoting appetite, and improving nutritional status in pediatric patients with idiopathic SMAS.
机译:目的:目前尚无严格保守治疗儿童特发性肠系膜上动脉综合征(SMAS)结局的可用数据。这项研究的目的是评估特发性SMAS儿童的临床和营养结果。患者与方法:对27例特发性SMAS患儿(上消化道)进行了为期1年的前瞻性观察研究,研究对象是特发性SMAS的儿童,他们接受了上消化道(UGI)系列检查,超声测量了主动脉肠系膜角度,进行了治疗,临床评估,生长评估以及12个月以上的定期临床拜访。结果:患者的平均年龄为11.77 +/- 2.15岁。主要的临床主诉是餐后疼痛或饱胀(88.9%),呕吐(55.6%)和早饱(51.9%)。八名患者(29.6%)体重减轻。 UGI系列揭示了SMAS的典型功能。超声的主动脉肠系膜角为10度至19度。大多数患者的身高(92.6%)高于第十个百分点,而15位患者(55.6%)的身高低于第十个百分点。 6例患者接受了手术干预(3例因梗阻而3例因体重减轻而持续厌食),其临床症状和体重状况在随访期间稳步改善。在21例未接受手术干预的患者中,有11例(52.4%)在治疗3个月后症状减轻> 50%,并且在治疗6个月后年龄体重百分位数显着增加。总体而言,仅在治疗6个月和12个月后,接受手术治疗或接受药物治疗的患者的年龄体重状况显着增加。结论:特发性SMAS患儿的主动脉肠系膜夹角<20度是一种持续现象。十二指肠空肠吻合术可有效缓解诸如厌食症等阻塞性症状并改善营养状况,而长期药物治疗可能有助于缓解特发性SMAS患儿的临床症状,增进食欲并改善营养状况。

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