便携式或可穿戴腹膜装置——腹膜透析的下一步发展方向?

Andrew Davenport
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引用次数: 0

摘要

腹膜透析可以被认为是一种“可穿戴”的透析疗法。然而,患者通常每天需要3或4次交换,每次需要20-40分钟,并且反复断开和重新连接可能增加感染的风险。尽管腹膜透析循环器允许患者从机器中“自由”13-15小时,但他们同样需要新鲜透析液的供应。因此,有几个小组探索了通过回收透析液来尽量减少透析液交换的可能性。然而,这种方法不仅带来了一系列挑战,包括废透析液的再生、酸碱和电解质平衡的维持以及足够的超滤,而且还需要克服新的障碍,包括监测吸附剂以确定何时超过容量。提出的维琴扎可穿戴人工肾脏系统由连续流动的腹膜透析系统组成,该系统结合了系列吸附剂和尿素酶,以在白天再生透析液,并在夜间进行7.5%的碘糊精交换。
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Portable or wearable peritoneal devices--the next step forward for peritoneal dialysis?

Peritoneal dialysis can be considered a "wearable" dialysis therapy. However, patients typically require 3 or 4 daily exchanges, each taking 20-40 minutes and potentially increasing the risk of infection by repeated disconnection and reconnection. Although peritoneal dialysis cyclers allow patients to be "free" from their machine for 13-15 hours, they similarly need a supply of fresh dialysate. Several groups have therefore explored the possibility of trying to minimize dialysate exchanges by recycling dialysate. However, that approach introduces not only a series of challenges, including regeneration of the spent dialysate, maintenance of acid-base and electrolyte balance and adequate ultrafiltration, but also new hurdles to be overcome, including monitoring the sorbents to determine when capacity is exceeded. The proposed Vicenza Wearable Artificial Kidney system consists of a continuous-flow peritoneal dialysis system that combines sorbents in series and urease to regenerate dialysate during the day, and a 7.5% icodextrin exchange overnight.

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Changes in Peritoneal Transport and Peritoneal Damage in Japanese Patients Undergoing Peritoneal Dialysis Using Neutral-pH Dialysate: A Retrospective Cohort Study at Two Centers. Maintaining Peritoneal Dialysis Adequacy: The Process of Incremental Prescription. Comparison of Various Scaling Parameters and Energy Expenditure in Peritoneal Dialysis Patients. Prevention of Peritoneal Dialysis Drop-Out. Accuracy of a Newly-Introduced Oscillometric Device for the Estimation of Arterial Stiffness Indices in Patients on Peritoneal Dialysis: A Preliminary Validation Study.
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