Wang Jinling, Yan Weihui, Lu Lina, Tao Yijing, Huang Liufang, Cai Wei, Wang Ying
Division of Pediatric Gastroenterology and Nutrition; Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai, China.
Front Surg. 2022 May 16;9:881782. doi: 10.3389/fsurg.2022.881782. eCollection 2022.
Type I short bowel syndrome (SBS) occurs after a critical reduction in the functional gut mass and resection of intestinal continuity after ileostomy or jejunostomy for necrotizing enterocolitis (NEC), intestinal atresia or other causes. SBS is often accompanied with intestinal failure-associated liver disease (IFALD) who requires long-term parenteral nutrition (PN). Our study aimed to observe the effect of intestinal continuity on the hepatic function of pediatric intestinal failure (IF) patients with type I SBS.
The pre-and post-anastomosis medical records of 35 pediatric patients with type I SBS from April 2013 to April 2019 were reviewed retrospectively. The average growth (cm/month) in the proximal and distal small bowel lengths was calculated as the growth in intestinal length (cm)/the duration (month) from enterostomy to anastomosis. The changes in hepatic function from enterostomy to anastomosis were evaluated by assessment of hepatic function before anastomosis for 6 weeks and after anastomosis for 4 weeks.
The average growth in proximal intestinal length was 9.3 cm/month (±7.2) in neonates and 2.8 cm/month (1.3, 11.9) in infants and children, and in distal intestinal length was 1.5 cm/month (0, 2.7) in neonates and 0.4 cm/month (0, 1.4) in infants and children. The incidence of IFALD was 28.6% 1 month before anastomosis and 20.0% 1 month after anastomosis ( < 0.05).
In pediatric type I SBS with IFALD, restoration of intestinal continuity may alleviate liver injury. There was an intestinal compensatory effect on the growth in the intestinal length after resection, and better results were seen in neonates in terms of intestinal length growth.
I型短肠综合征(SBS)发生于因坏死性小肠结肠炎(NEC)、肠闭锁或其他原因行回肠造口术或空肠造口术后功能性肠管质量严重减少及肠管连续性中断之后。SBS常伴有需要长期肠外营养(PN)的肠衰竭相关肝病(IFALD)。我们的研究旨在观察肠管连续性对I型SBS小儿肠衰竭(IF)患者肝功能的影响。
回顾性分析2013年4月至2019年4月35例I型SBS小儿患者吻合术前和术后的病历。近端和远端小肠长度的平均生长速度(cm/月)计算为肠管长度生长值(cm)/从肠造口术至吻合术的持续时间(月)。通过评估吻合术前6周和吻合术后4周的肝功能来评价从肠造口术至吻合术期间肝功能的变化。
新生儿近端肠管长度平均生长速度为9.3 cm/月(±7.2),婴幼儿为2.8 cm/月(1.3,11.9);新生儿远端肠管长度平均生长速度为1.5 cm/月(0,2.7),婴幼儿为0.4 cm/月(0,1.4)。吻合术前1个月IFALD的发生率为28.6%,吻合术后1个月为20.0%(P<0.05)。
在伴有IFALD的小儿I型SBS中,恢复肠管连续性可能减轻肝损伤。切除术后肠管长度生长存在肠代偿效应,且在肠管长度生长方面新生儿的效果更佳。