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一种含左旋肉碱和木糖醇的新型腹膜透析液用于持续性非卧床腹膜透析患者:首次临床经验

A New Peritoneal Dialysis Solution Containing L-Carnitine and Xylitol for Patients on Continuous Ambulatory Peritoneal Dialysis: First Clinical Experience.

作者信息

Rago Carmela, Lombardi Teresa, Di Fulvio Giorgia, Di Liberato Lorenzo, Arduini Arduino, Divino-Filho José C, Bonomini Mario

机构信息

Nephrology and Dialysis Unit, Department of Medicine, G. D'Annunzio University of Chieti-Pescara, SS. Annunziata Hospital, Via dei Vestini, 66013 Chieti, Italy.

Department of Research and Development, Iperboreal Pharma, 65100 Pescara, Italy.

出版信息

Toxins (Basel). 2021 Feb 24;13(3):174. doi: 10.3390/toxins13030174.

Abstract

Peritoneal dialysis (PD) is a feasible and effective renal replacement therapy (RRT) thanks to the dialytic properties of the peritoneal membrane (PM). Preservation of PM integrity and transport function is the key to the success of PD therapy, particularly in the long term, since the prolonged exposure to unphysiological hypertonic glucose-based PD solutions in current use is detrimental to the PM, with progressive loss of peritoneal ultrafiltration capacity causing technique failure. Moreover, absorbing too much glucose intraperitoneally from the dialysate may give rise to a number of systemic metabolic effects. Here we report the preliminary results of the first clinical experience based on the use in continuous ambulatory PD (CAPD) patients of novel PD solutions obtained through partly replacing the glucose load with other osmotically active metabolites, such as L-carnitine and xylitol. Ten CAPD patients were treated for four weeks with the new solutions. There was good tolerance to the experimental PD solutions, and no adverse safety signals were observed. Parameters of dialysis efficiency including creatinine clearance and urea Kt/V proved to be stable as well as fluid status, diuresis, and total peritoneal ultrafiltration. The promising tolerance and local/systemic advantages of using L-carnitine and xylitol in the PD solution merit further research.

摘要

由于腹膜(PM)的透析特性,腹膜透析(PD)是一种可行且有效的肾脏替代疗法(RRT)。保持PM的完整性和转运功能是PD治疗成功的关键,特别是从长期来看,因为目前使用的基于非生理性高渗葡萄糖的PD溶液长时间接触对PM有害,会导致腹膜超滤能力逐渐丧失,从而引起技术失败。此外,从透析液中腹膜内吸收过多葡萄糖可能会产生许多全身代谢影响。在此,我们报告了首例临床经验的初步结果,该经验基于在持续非卧床腹膜透析(CAPD)患者中使用通过用其他具有渗透活性的代谢物(如L-肉碱和木糖醇)部分替代葡萄糖负荷而获得的新型PD溶液。10名CAPD患者使用新溶液治疗了四周。对实验性PD溶液耐受性良好,未观察到不良安全信号。包括肌酐清除率和尿素Kt/V在内的透析效率参数以及液体状态、尿量和总腹膜超滤均保持稳定。在PD溶液中使用L-肉碱和木糖醇所具有的良好耐受性以及局部/全身优势值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f74/7996173/504b2283451f/toxins-13-00174-g001.jpg

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