Derikx Joep P M, van Waardenburg Dick A, Thuijls Geertje, Willigers Henriëtte M, Koenraads Marianne, van Bijnen Annemarie A, Heineman Erik, Poeze Martijn, Ambergen Ton, van Ooij André, van Rhijn Lodewijk W, Buurman Wim A
Department of Surgery, University Hospital Maastricht & Nutrition and Toxicology Research Institute (NUTRIM), Maastricht University, Maastricht, the Netherlands.
PLoS One. 2008;3(12):e3954. doi: 10.1371/journal.pone.0003954. Epub 2008 Dec 17.
Gut barrier loss has been implicated as a critical event in the occurrence of postoperative complications. We aimed to study the development of gut barrier loss in patients undergoing major non-abdominal surgery.
METHODOLOGY/PRINCIPAL FINDINGS: Twenty consecutive children undergoing spinal fusion surgery were included. This kind of surgery is characterized by long operation time, significant blood loss, prolonged systemic hypotension, without directly leading to compromise of the intestines by intestinal manipulation or use of extracorporeal circulation. Blood was collected preoperatively, every two hours during surgery and 2, 4, 15 and 24 hours postoperatively. Gut mucosal barrier was assessed by plasma markers for enterocyte damage (I-FABP, I-BABP) and urinary presence of tight junction protein claudin-3. Intestinal mucosal perfusion was measured by gastric tonometry (P(r)CO2, P(r-a)CO2-gap). Plasma concentration of I-FABP, I-BABP and urinary expression of claudin-3 increased rapidly and significantly after the onset of surgery in most children. Postoperatively, all markers decreased promptly towards baseline values together with normalisation of MAP. Plasma levels of I-FABP, I-BABP were significantly negatively correlated with MAP at (1/2) hour before blood sampling (-0.726 (p<0.001), -0.483 (P<0.001), respectively). Furthermore, circulating I-FABP correlated with gastric mucosal P(r)CO2, P(r-a)CO2-gap measured at the same time points (0.553 (p = 0.040), 0.585 (p = 0.028), respectively).
CONCLUSIONS/SIGNIFICANCE: This study shows the development of gut barrier loss in children undergoing major non-abdominal surgery, which is related to preceding hypotension and mesenterial hypoperfusion. These data shed new light on the potential role of peroperative circulatory perturbation and intestinal barrier loss.
肠道屏障功能丧失被认为是术后并发症发生的关键事件。我们旨在研究接受大型非腹部手术患者肠道屏障功能丧失的发展情况。
方法/主要发现:纳入连续20例接受脊柱融合手术的儿童。这类手术的特点是手术时间长、失血量大、全身性低血压持续时间长,且不会因肠道操作或使用体外循环直接导致肠道受损。术前、术中每两小时以及术后2、4、15和24小时采集血液。通过血浆中肠上皮细胞损伤标志物(I-FABP、I-BABP)以及尿中紧密连接蛋白claudin-3的存在情况评估肠道黏膜屏障。通过胃张力测定法(P(r)CO2、P(r-a)CO2差值)测量肠道黏膜灌注。大多数儿童在手术开始后,血浆中I-FABP、I-BABP浓度以及尿中claudin-3表达迅速且显著增加。术后,所有标志物迅速降至基线值,同时平均动脉压恢复正常。在采血前半小时,血浆I-FABP、I-BABP水平与平均动脉压显著负相关(分别为-0.726(p<0.001)、-0.483(P<0.001))。此外,循环中的I-FABP与同一时间点测量的胃黏膜P(r)CO2、P(r-a)CO2差值相关(分别为0.553(p = 0.040)、0.585(p = 0.028))。
结论/意义:本研究显示接受大型非腹部手术的儿童存在肠道屏障功能丧失,这与术前低血压和肠系膜灌注不足有关。这些数据为围手术期循环紊乱和肠道屏障功能丧失的潜在作用提供了新的线索。