Froghi Farid, Gopalan Vignesh, Anastasiou Zachos, Koti Rahul, Gurusamy Kurinchi, Eastgate Christine, McNeil Margaret, Filipe Helder, Pinto Manuel, Singh Jeshika, Longworth Louise, Mallett Susan, Schofield Nick, Thorburn Douglas, Martin Daniel, Davidson Brian R
UCL Division of Surgery & Interventional Sciences, HPB and Liver Transplantation, London, United Kingdom UCL Joint Research Office, Biostatistics Group, London, United Kingdom Royal Free Hospital, Critical Care Unit, London, United Kingdom PHMR Limited, London, United Kingdom UCL Institute for Liver and Digestive Health, London, United Kingdom UCL Division of Surgery & Interventional Sciences, London, United Kingdom Peninsula Medical School, University of Plymouth, Plymouth, United Kingdom.
Int J Surg. 2022 Mar;99:106265. doi: 10.1016/j.ijsu.2022.106265. Epub 2022 Feb 15.
Goal-directed fluid therapy (GDFT) has been shown to reduce the complications following a variety of major surgical procedures, possibly mediated by improved organ perfusion and function. We have shown that it is feasible to randomise patients to GDFT or standard fluid management following liver transplant in the cardiac-output optimisation following liver transplantation (COLT) trial. The current study compares end organ function in patients from the COLT trial who received GDFT in comparison to those receiving standard care (SC) following liver transplant.
Adult patients with liver cirrhosis undergoing liver transplantation were randomised to GDFT or SC for the first 12 h following surgery as detailed in a published trial protocol. GDFT protocol was based on stroke volume (SV) optimisation using 250 ml crystalloid boluses. Total fluid administration and time to extubation were recorded. Hourly SV and cardiac output (CO) readings were recorded from the non-invasive cardiac output monitoring (NICOM) device in both groups. Pulmonary function was assessed by arterial blood gas (ABG) and ventilatory parameters. Lung injury was assessed using PaO:FiO ratios and calculated pulmonary compliance. The KDIGO score was used for determining acute kidney injury. Renal and liver graft function were assessed during the post-operative period and at 3 months and 1-year.
60 patients were randomised to GDFT (n = 30) or SC (n = 30). All patients completed the 12 h intervention period. GDFT group received a significantly higher total volume of fluid during the 12 h trial intervention period (GDFT 5317 (2335) vs. SC 3807 (1345) ml, p = 0.003); in particular crystalloids (GDFT 3968 (2073) vs. SC 2510 (1027) ml, p = 0.002). There was no evidence of significant difference between the groups in SV or CO during the assessment periods. Time to extubation, PaO2: FIO ratios, pulmonary compliance, ventilatory or blood gas measurements were similar in both groups. There was a significant rise in serum creatinine from baseline (77 μmol/L) compared to first (87 μmol/L, p = 0.039) and second (107 μmol/L, p = 0.001) post-operative days. There was no difference between GDFT and SC in the highest KDIGO scores for the first 7 days post-LT. At 1-year follow-up, there was no difference in need for renal replacement therapy or graft function.
In this randomised trial of fluid therapy post liver transplant, GDFT was associated with an increased volume of crystalloids administered but did not alter early post-operative pulmonary or renal function when compared with standard care.
目标导向液体治疗(GDFT)已被证明可减少各种大型外科手术后的并发症,这可能是通过改善器官灌注和功能来介导的。我们已经表明,在肝移植心脏输出优化(COLT)试验中,将患者随机分为接受GDFT或标准液体管理是可行的。本研究比较了COLT试验中接受GDFT的患者与接受肝移植后标准护理(SC)的患者的终末器官功能。
肝硬化成年患者在肝移植手术后的前12小时被随机分为GDFT组或SC组,具体分组如已发表的试验方案所述。GDFT方案基于使用250ml晶体液推注优化每搏输出量(SV)。记录总液体输入量和拔管时间。两组均通过无创心输出量监测(NICOM)设备记录每小时的SV和心输出量(CO)读数。通过动脉血气(ABG)和通气参数评估肺功能。使用PaO₂:FiO₂比值和计算的肺顺应性评估肺损伤。KDIGO评分用于确定急性肾损伤。在术后期间、3个月和1年时评估肾脏和肝脏移植功能。
60例患者被随机分为GDFT组(n = 30)或SC组(n = 30)。所有患者均完成了12小时的干预期。在12小时的试验干预期内,GDFT组接受的总液体量显著更高(GDFT组为5317(2335)ml,SC组为3807(1345)ml,p = 0.003);尤其是晶体液(GDFT组为3968(2073)ml,SC组为2510(1027)ml,p = 0.002)。在评估期间,两组之间的SV或CO没有显著差异的证据。两组的拔管时间、PaO₂:FiO₂比值、肺顺应性、通气或血气测量结果相似。与术后第一天(87μmol/L,p = 0.039)和第二天(107μmol/L,p = 0.001)相比,血清肌酐从基线(77μmol/L)有显著升高。肝移植后前7天,GDFT组和SC组的最高KDIGO评分没有差异。在1年随访时,肾脏替代治疗需求或移植功能没有差异。
在这项肝移植后液体治疗的随机试验中,与标准护理相比,GDFT与晶体液输入量增加有关,但并未改变术后早期的肺或肾功能。