Wasa M, Takagi Y, Sando K, Harada T, Okada A
Department of Pediatric Surgery, Osaka University Medical School, Japan.
Eur J Pediatr Surg. 1999 Aug;9(4):207-9. doi: 10.1055/s-2008-1072245.
The purpose of this study is to evaluate 12 pediatric short-bowel syndrome (SBS) patients experienced at Osaka University Hospital and its affiliated hospitals and to study the intestinal length for achieving intestinal adaptation and the metabolic characteristics. The length of the residual small intestine ranged from 0 to 75 cm with an average of 47 cm and an ileocecal valve had been resected in five cases. Total parenteral nutrition (TPN) was started immediately after operation and was gradually substituted by enteral nutrition. No patient died during the follow-up period. Eight of 12 patients could be weaned from TPN with residual intestinal length of 27 to 75 cm (mean 57 cm). Four patients with the residual intestine of 0 to 45 cm (mean 22 cm) were unable to achieve intestinal adaptation. The rate of catheter-related sepsis per 1000 catheter days was 0.63. Fatty liver was detected in two cases, but no patient developed progressive liver failure. Plasma arginine and citrulline were decreased in patients who were unable to achieve intestinal adaptation. Our nutritional support program provided excellent survival for pediatric SBS patients primarily due to the low incidence of catheter-related sepsis and no episode of severe liver disease. Patients with more than 16 cm of residual intestinal length can be expected to be weaned from TPN.
本研究旨在评估大阪大学医院及其附属医院收治的12例小儿短肠综合征(SBS)患者,研究实现肠道适应所需的肠长度及代谢特征。残余小肠长度为0至75厘米,平均47厘米,5例患者的回盲瓣已被切除。术后立即开始全胃肠外营养(TPN),并逐渐被肠内营养替代。随访期间无患者死亡。12例患者中有8例在残余肠长度为27至75厘米(平均57厘米)时能够停用TPN。4例残余肠长度为0至45厘米(平均22厘米)的患者未能实现肠道适应。每1000导管日的导管相关败血症发生率为0.63。2例患者检测出脂肪肝,但无患者发生进行性肝衰竭。未能实现肠道适应的患者血浆精氨酸和瓜氨酸水平降低。我们的营养支持方案为小儿SBS患者提供了良好的生存率,主要是因为导管相关败血症的发生率低且无严重肝病发作。残余肠长度超过16厘米的患者有望停用TPN。