Division of Pediatric Gastroenterology, Department of Pediatrics, Chang Gung Children's Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
J Pediatr Gastroenterol Nutr. 2010 Aug;51(2):177-82. doi: 10.1097/MPG.0b013e3181c7bdda.
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.
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.
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.
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.
对于严格保守治疗的儿童特发性肠系膜上动脉综合征(SMAS),尚无相关结局数据。本研究旨在评估特发性 SMAS 患儿的临床和营养结局。
对 27 例特发性 SMAS 患儿进行了为期 1 年的前瞻性观察研究,评估治疗效果和结局。所有患儿均行上消化道(UGI)系列检查、腹主动脉肠系膜夹角超声测量、治疗、临床评估、生长评估,并定期随访超过 12 个月。
患儿平均年龄为 11.77±2.15 岁。主要临床症状为餐后疼痛或饱胀(88.9%)、呕吐(55.6%)和早饱(51.9%)。8 例(29.6%)患儿出现体重减轻。UGI 系列检查显示 SMAS 的典型特征。超声检查腹主动脉肠系膜夹角为 10°~19°。大多数患儿(92.6%)的身高均位于第 10 百分位以上,而 15 例(55.6%)患儿的体重低于第 10 百分位。6 例患儿接受了手术干预(3 例因梗阻,3 例因持续厌食伴体重减轻),其临床症状和体重状况在随访期间逐渐改善。21 例未接受手术干预的患儿中,有 11 例(52.4%)患儿在治疗 3 个月后症状缓解超过 50%,治疗 6 个月后体重/年龄百分位明显增加。总体而言,接受手术治疗或仅药物治疗的患儿在治疗 6 个月和 12 个月后体重/年龄百分位均显著增加。
儿童特发性 SMAS 存在恒定的腹主动脉肠系膜夹角<20°现象。空肠十二指肠吻合术可有效缓解厌食等梗阻症状,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,促进食欲,改善营养状况。