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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Cardiac output-based fluid optimization for kidney transplant recipients: a proof-of-concept trial
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Cardiac output-based fluid optimization for kidney transplant recipients: a proof-of-concept trial

机译:基于心脏输出的肾移植受者的流体优化:概念验证试验

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摘要

Purpose Intravenous fluid management for deceased donor kidney transplantation is an important, modifiable risk factor for delayed graft function (DGF). The primary objective of this study was to determine if goal-directed fluid therapy using esophageal Doppler monitoring (EDM) to optimize stroke volume (SV) would alter the amount of fluid given. Methods This randomized, proof-of-concept trial enrolled 50 deceased donor renal transplant recipients. Data collected included patient characteristics, fluid administration, hemodynamics, and complications. The EDM was used to optimize SV in the EDM group. In the control group, fluid management followed the current standard of practice. The groups were compared for the primary outcome of total intraoperative fluid administered. Results There was no difference in the mean (standard deviation) volume of intraoperative fluid administered to the 24 control and 26 EDM patients [2,307 (750) mL vs 2,675 (842) mL, respectively; mean difference, 368 mL; 95% confidence interval (CI), ??87 to +?823; P ?=?0.11]. The incidence of complications in the control and EDM groups was similar (15/24 vs 17/26, respectively; P ?=?0.99), as was the incidence of delayed graft failure (8/24 vs 11/26, respectively; P ?=?0.36). Conclusions Goal-directed fluid therapy did not alter the volume of fluid administered or the incidence of complications. This proof-of-concept trial provides needed data for conducting a larger trial to determine the influence of fluid therapy on the incidence in DGF in deceased donor kidney transplantation. Trial registration www.clinicaltrials.gov (NCT02512731). Registered 31 July 2015.
机译:目的静脉内流体管理用于死亡的供体肾移植是延迟移植功能(DGF)的重要危险因素。本研究的主要目的是确定使用食道多普勒监测(EDM)进行优化中风体积(SV)的目标定向的流体治疗将改变给定的流体量。方法采用随机,概念验证试验,已注册50名已故的供体肾移植受体。收集的数据包括患者特征,流体给药,血液动力学和并发症。 EDM用于优化EDM组中的SV。在对照组中,流体管理遵循当前的实践标准。比较群体,以施用总术中流体的主要结果。结果施用于24对照的术中流体的平均值(标准偏差)体积没有差异,26例EDM患者分别[2,307(750)mL与2,675(842)mL。平均差异,368毫升; 95%置信区间(CI),?? 87至+?823; p?=?0.11]。对照和EDM组并发症的发病率为类似(分别为15/24 Vs 17/26; p?= 0.99),延迟移植衰竭的发生率(分别为8/24 vs 11/26; p ?=?0.36)。结论目标导向的液体疗法没有改变施用的流体体积或并发症的发生率。该概念证据证明提供了需要进行更大的试验的所需数据,以确定流体治疗对死者肾移植中DGF发病率的影响。试用注册www.clinicaltrials.gov(nct02512731)。注册2015年7月31日。

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