Joosten Alexandre, Hafiane Reda, Pustetto Marco, Van Obbergh Luc, Quackels Thierry, Buggenhout Alexis, Vincent Jean-Louis, Ickx Brigitte, Rinehart Joseph
Department of Anesthesiology, CUB Erasme, Hopital ERASME, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.
Department of Urology, CUB Erasme, Université Libre de Bruxelles, 808, route de Lennik, 1070, Brussels, Belgium.
J Clin Monit Comput. 2019 Feb;33(1):15-24. doi: 10.1007/s10877-018-0156-x. Epub 2018 May 19.
The purpose of this study was to assess the effects of using a real time clinical decision-support system, "Assisted Fluid Management" (AFM), to guide goal-directed fluid therapy (GDFT) during major abdominal surgery. We compared a group of patients managed using the AFM system with a historical cohort of patients (control group) who had been managed using a manual GDFT strategy. Adherence to the protocol was defined as the relative intraoperative time spent with a stroke volume variation (SVV) < 13%. We hypothesised that patients in the AFM group would have more time during surgery with a SVV < 13% compared to the control group. All patients had a radial arterial line connected to a pulse contour analysis monitor and received a 2 ml/kg/h maintenance crystalloid infusion. Additional 250 ml crystalloid boluses were administered whenever measured SVV ≥ 13% in the control group, and when the software suggested a fluid bolus in the AFM group. We compared 46 AFM-guided patients to 38 controls. Patients in the AFM group spent significantly more time during surgery with a SVV < 13% compared to the control group (median 92% [82, 96] vs. 76% [54, 86]; P < 0.0005), and received less fluid overall (1775 ml [1225, 2425] vs. 2350 ml [1825, 3250]; P = 0.010). The incidence of postoperative complications was comparable in the two groups. Implementation of a decision support system for GDFT guidance resulted in a significantly longer period during surgery with a SVV < 13% with a reduced total amount of fluid administered. Trial registration: Clinical Trials.gov (NCT03141411).
本研究的目的是评估使用实时临床决策支持系统“辅助液体管理”(AFM)在腹部大手术期间指导目标导向液体治疗(GDFT)的效果。我们将一组使用AFM系统管理的患者与一组采用手动GDFT策略管理的历史队列患者(对照组)进行了比较。对方案的依从性定义为术中每搏量变异(SVV)<13%的相对时间。我们假设与对照组相比,AFM组患者在手术期间SVV<13%的时间更多。所有患者均连接桡动脉导管至脉搏轮廓分析监测仪,并接受2ml/kg/h的维持性晶体液输注。在对照组中,每当测量的SVV≥13%时给予额外250ml晶体液推注,在AFM组中则在软件提示时给予液体推注。我们将46例AFM指导下的患者与38例对照组患者进行了比较。与对照组相比,AFM组患者在手术期间SVV<13%的时间显著更长(中位数92%[82,96]对76%[54,86];P<0.0005),且总体液体摄入量更少(1775ml[1225,2425]对2350ml[1825,3250];P=0.010)。两组术后并发症的发生率相当。实施用于GDFT指导的决策支持系统导致手术期间SVV<13%的时间显著延长,同时液体总摄入量减少。试验注册:ClinicalTrials.gov(NCT03141411)。