de Witte Piet, de Witt Christien A, van de Minkelis Johan L, Boerma Djamila, Solinger H Frank, Hack C Erik, Bruins Peter
Department of Anesthesiology, Intensive Care & Pain Management, St Antonius Ziekenhuis, Nieuwegein, The Netherlands.
Department of Anesthesiology & Pain Management, Medisch Centrum, Alkmaar, The Netherlands.
J Gastrointest Oncol. 2019 Apr;10(2):244-253. doi: 10.21037/jgo.2018.12.09.
Surgical cytoreduction and simultaneous hyperthermic intraoperative intraperitoneal chemotherapy (HIPEC) for peritoneal carcinomatosis has a high incidence of postoperative complications. Inadequate intraoperative volume therapy is a known risk factor for the development of postoperative complications. Another possible risk factor is the inflammatory response due to surgery and HIPEC. The aim of this observational pilot study was to monitor fluid intake in the first 24 hours peri- and postoperative by using a non-invasive cardiac output indicator. Furthermore, we measured circulating cytokines and evaluated the possible relation of these changes of inflammatory response with the non-invasive monitored fluid management.
Twenty-four patients undergoing cytoreductive surgery and HIPEC for peritoneal carcinomatosis were included. Patients were randomised into either a liberal fluid management group using intra-arterial blood pressure and central venous pressure measurement or a restrictive group by using intra-arterial blood pressure and central venous pressure measurement with FloTrac/Vigileo monitoring. Cytokines were measured with multiplex immunoassays.
We found no difference in the amount of fluid administration in patients undergoing HIPEC surgery with FloTrac/Vigileo monitoring compared to standard care. Furthermore, there was no difference in mortality, ICU and hospital length of stay between both groups. A severe inflammatory response was seen in all patients after the HIPEC procedure with a rapid increase of interleukins and C-reactive protein (CRP). There was however no difference between our intervention and control group in the severity of this reaction. Finally, we found no relation between the severity of the inflammatory response and mortality, or a composite end-point of mortality and severe complications within 30 days postoperative.
FloTrac/Vigileo monitoring does not lead to a more restrictive fluid administration and does not influence short-term clinical course in patients undergoing HIPEC surgery. The procedure itself leads to a severe inflammatory response, which is not affected by the use of FloTrac/Vigileo. Our data do not support the use of FloTrac/Vigileo monitoring in patients undergoing HIPEC surgery concerning fluid restrictive management.
手术细胞减灭术联合术中同步热灌注腹腔化疗(HIPEC)治疗腹膜癌病术后并发症发生率较高。术中液体治疗不足是术后并发症发生的已知危险因素。另一个可能的危险因素是手术和HIPEC引起的炎症反应。本观察性试点研究的目的是通过使用无创心输出量指标监测围手术期及术后24小时内的液体摄入量。此外,我们测量了循环细胞因子,并评估了这些炎症反应变化与无创监测液体管理之间的可能关系。
纳入24例行腹膜癌病细胞减灭术和HIPEC的患者。患者被随机分为自由液体管理组(使用动脉血压和中心静脉压测量)或限制性组(使用动脉血压和中心静脉压测量并结合FloTrac/Vigileo监测)。采用多重免疫分析法测量细胞因子。
我们发现,与标准护理相比,使用FloTrac/Vigileo监测的HIPEC手术患者的液体输注量没有差异。此外,两组之间的死亡率、重症监护病房(ICU)住院时间和住院时间均无差异。所有患者在HIPEC手术后均出现严重炎症反应,白细胞介素和C反应蛋白(CRP)迅速升高。然而,我们的干预组和对照组在这种反应的严重程度上没有差异。最后,我们发现炎症反应的严重程度与死亡率或术后30天内死亡率和严重并发症的复合终点之间没有关系。
FloTrac/Vigileo监测不会导致更严格的液体输注,也不会影响接受HIPEC手术患者的短期临床病程。手术本身会导致严重的炎症反应,不受FloTrac/Vigileo使用的影响。我们的数据不支持在接受HIPEC手术的患者中使用FloTrac/Vigileo监测进行液体限制管理。