Hukkinen Maria, Merras-Salmio Laura, Sipponen Taina, Mutanen Annika, Rintala Risto J, Mäkisalo Heikki, Pakarinen Mikko P
Pediatric Liver and Gut Research Group, University of Helsinki , Helsinki , Finland.
Scand J Gastroenterol. 2015 Feb;50(2):153-61. doi: 10.3109/00365521.2014.962607. Epub 2014 Nov 25.
This is a descriptive study aiming to compare outcomes of intestinal rehabilitation surgery among pediatric and adult intestinal failure (IF) patients with either primary intestinal motility disorders or short bowel syndrome (SBS) treated by our nationwide program.
Medical records of IF patients (n = 31, 71% children) having undergone autologous intestinal reconstructions (AIR) (n = 25), intestinal transplantation (ITx) (n = 5), or being listed for ITx (n = 2) between 1994 and 2014 were reviewed.
At surgery, median age was 3.4 (interquartile range, 1.0-22.1) in SBS (n = 22) and 16.5 (3.2-26.7) years in dysmotility patients (n = 9) who received median 60% and 83% of energy requirement parenterally, respectively. Median small bowel length was shorter in SBS than dysmotility patients (34 versus 157 cm, p < 0.001). Following AIR, none of the dysmotility patients achieved permanent intestinal autonomy, whereas 68% of SBS patients weaned off parenteral nutrition (PN) (p = 0.022) and none required listing for ITx. Five dysmotility patients who underwent ITx achieved intestinal autonomy. Regarding both AIR and ITx procedures, no significant difference in PN weaning was observed between the two subgroups. At last follow-up, 3.3 (0.6-8.0) years postoperatively, median plasma bilirubin was 6 (4-16) µmol/l, while liver biopsy showed fibrosis (Metavir stage 1-2) in 50% and cholestasis in 8%. Proportion of PN energy requirement had reduced significantly (p = 0.043) among PN-dependent SBS (n = 7) but not among dysmotility patients (n = 5). Overall survival was 90%.
AIR surgery was beneficial among selected SBS patients, whereas in intestinal dysmotility disorders, permanent PN weaning was only achieved by ITx.
本研究为描述性研究,旨在比较在我们的全国性项目中接受治疗的患有原发性肠道动力障碍或短肠综合征(SBS)的儿科和成人肠衰竭(IF)患者肠道康复手术的结果。
回顾了1994年至2014年间接受自体肠道重建(AIR)(n = 25)、肠道移植(ITx)(n = 5)或列入ITx名单(n = 2)的IF患者(n = 31,71%为儿童)的医疗记录。
手术时,SBS患者(n = 22)的中位年龄为3.4岁(四分位间距,1.0 - 22.1),动力障碍患者(n = 9)的中位年龄为16.5岁(3.2 - 26.7),他们分别通过肠外途径获得了60%和83%的能量需求。SBS患者的中位小肠长度短于动力障碍患者(34 cm对157 cm,p < 0.001)。AIR术后,动力障碍患者均未实现永久性肠道自主,而68%的SBS患者停用了肠外营养(PN)(p = 0.022),且无人需要列入ITx名单。5例接受ITx的动力障碍患者实现了肠道自主。关于AIR和ITx手术,两个亚组之间在PN撤减方面未观察到显著差异。在术后3.3(0.6 - 8.0)年的最后随访中,中位血浆胆红素为6(4 - 16)µmol/l,而肝活检显示50%的患者有纤维化(梅塔维分级1 - 2级),8%的患者有胆汁淤积。在依赖PN的SBS患者(n = 7)中,PN能量需求比例显著降低(p = 0.043),但在动力障碍患者(n = 5)中未降低。总体生存率为90%。
AIR手术对部分选定的SBS患者有益,而在肠道动力障碍疾病中,仅通过ITx实现了永久性PN撤减。