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Enhancement of solute clearance using pulsatile push-pull dialysate flow for the Quanta SC+: A novel clinic-to-home haemodialysis system

机译:使用脉动推拉透析液对Quanta Sc +的溶质清除的提高+:一种新型临床 - 家庭血液透析系统

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摘要

BACKGROUND AND OBJECTIVE:The SC+ haemodialysis system developed by Quanta Dialysis Technologies is a small, easy-to-use dialysis system designed to improve patient access to self-care and home haemodialysis. A prototype variant of the standard SC+ device with a modified fluidic management system generating a pulsatile push-pull dialysate flow through the dialyser during use has been developed for evaluation. It was hypothesized that, as a consequence of the pulsatile push-pull flow through the dialyser, the boundary layers at the membrane surface would be disrupted, thereby enhancing solute transport across the membrane, modifying protein fouling and maintaining the surface area available for mass and fluid transport throughout the whole treatment, leading to solute transport (clearance) enhancement compared to normal haemodialysis (HD) operation. METHODS:The pumping action of the SC+ system was modified by altering the sequence and timings of the valves and pumps associated with the flow balancing chambers that push and pull dialysis fluid to and from the dialyser. Using this unique prototype device, solute clearance performance was assessed across a range of molecular weights in two related series of laboratory bench studies. The first measured dialysis fluid moving across the dialyser membrane using ultrasonic flowmeters to establish the validity of the approach; solute clearance was subsequently measured using fluorescently tagged dextran molecules as surrogates for uraemic toxins. The second study used human blood doped with uraemic toxins collected from the spent dialysate of dialysis patients to quantify solute transport. In both, the performance of the SC+ prototype was assessed alongside reference devices operating in HD and pre-dilution haemodiafiltration (HDF) modes. RESULTS:Initial testing with fluorescein-tagged dextran molecules (0.3 kDa, 4 kDa, 10 kDa and 20 kDa) established the validity of the experimental pulsatile push-pull operation in the SC+ system to enhance clearance and demonstrated a 10 to 15% improvement above the current HD mode used in clinic today. The magnitude of the observed enhancement compared favourably with that achieved using pre-dilution HDF with a substitution fluid flow rate of 60 mL/min (equivalent to a substitution volume of 14.4 L in a 4-hour session) with the same dialyser and marker molecules. Additional testing using human blood indicated a comparable performance to pre-dilution HDF; however, in contrast with HDF, which demonstrated a gradual decrease in solute removal, the clearance values using the pulsatile push-pull method on the SC+ system were maintained over the entire duration of treatment. Overall albumin losses were not different. CONCLUSIONS:Results obtained using an experimental pulsatile push-pull dialysis flow configuration with an aqueous blood analogue and human blood ex vivo demonstrate an enhancement of solute transport across the dialyser membrane. The level of enhancement makes this approach comparable with that achieved using pre-dilution HDF with a substitution fluid flow rate of 60 mL/min (equivalent to a substitution volume of 14.4 L in a 4-hour session). The observed enhancement of solute transport is attributed to the disruption of the boundary layers at the fluid-membrane interface which, when used with blood, minimizes protein fouling and maintains the surface area.
机译:背景与目的:通过广达透析技术开发的SC +血液透析系统是一个小的,易于使用的透析系统,旨在提高自我保健和家庭血液透析病人的访问。具有修饰的流体管理系统中生成通过在使用过程中透析脉动推挽透析液流量的标准SC +器件的原型的变体已被开发用于评估。有人推测,如通过透析搏动推挽流的结果,在膜表面上的边界层会被破坏,从而提高穿过膜溶质运输,修饰蛋白结垢和维护的表面面积可用于大规模和在整个治疗流体输送,导致溶质运移(间隙)增强比较正常的血液透析(HD)操作。方法:将SC +系统的泵送作用是通过改变序列和阀的定时修改和泵与所述流动平衡该推室和拉透析液和从透析器相关联。使用这种独特的原型设备,溶质清除性能跨分子量范围的两个相关系列实验台的研究评估。横跨使用超声波流量计来建立方法的有效性的透析膜的第一测量透析流体移动;使用荧光标记的葡聚糖分子作为替代物尿毒症毒素溶质清除随后测量。第二项研究中使用的人血掺杂与透析患者的废透析液收集尿毒症毒素量化溶质运移。在这两个中,SC +原型的性能进行了评估一起参考设备在HD操作和预稀释血液透析滤过(HDF)模式。结果:与建立的SC +系统,以提高清除实验脉动推拉操作的有效性和证明高于10至15%的改进的荧光素标记的葡聚糖分子(0.3千道尔顿,4千道尔顿,10千道尔顿和20千道尔顿)初始试验目前HD模式目前在临床上使用。所观察到的增强的幅度相比,毫不逊色,使用预稀释HDF以60毫升/分钟(相当于14.4 L的一个4小时的会议的取代量)的取代流体流速用相同透析和标记分子来实现。使用人血液额外的测试指示的相当的性能预先稀释HDF;然而,在具有HDF,这表明在溶质除去逐渐减少相反,使用SC +系统上的脉动推挽法的清除率值维持在治疗的整个持续时间。总体白蛋白损失差异不显着。结论:使用与水性血类似物和人血体外实验脉动推挽透析流配置获得的结果表明在整个透析膜溶质运输的增强。增强的级别使得使用预稀释HDF以60毫升/分钟(相当于14.4 L的4小时会话的取代量)的取代流体流速来实现这种方法与相媲美。溶质运输的所观察到的增强的流体膜界面,其与血液,最小化蛋白质结垢使用和维护时的表面积归因于边界层的破坏。

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