Literature DB >> 11229612

Biocompatibility of new peritoneal dialysis solutions: clinical experience.

E Garcia-Lopez1, B Lindholm, A Tranaeus.   

Abstract

The successful development of peritoneal dialysis (PD) during the last two decades has been made possible by using well-established glucose-based solutions with lactate as buffer. On the other hand, awareness has been increasing about the potentially negative effects of the high concentrations of glucose and lactate, and the low pH of conventional PD solutions. This awareness has prompted an intensive effort to search for and test alternative solutions. As a result, three new, more biocompatible solutions-containing either less glucose or less lactate--are available. Amino acid-based solution uses amino acids instead of glucose as the osmotic agent; it is indicated for treatment of malnutrition. The higher pH and absence of glucose in this solution may prevent alterations of the peritoneal membrane caused by acidity and high glucose concentrations. Bicarbonate/lactate-buffered solution contains a physiologic concentration of bicarbonate and a reduced concentration of lactate; it also has a physiologic pH and markedly reduced levels of glucose degradation products (GDPs). Icodextrin-based solution contains icodextrin as the osmotic agent; it is indicated for long dwells, delivering sustained ultrafiltration for more than 16 hours. This iso-osmolar glucose-free solution may reduce peritoneal membrane alterations caused by glucose or the hyperosmolality (or both) of conventional solutions. Clinical experience of the new solutions is now extensive, and their efficacy and safety are well documented. It therefore seems appropriate to state that we have entered a new era of PD therapy. Each of the new solutions may be less damaging to the peritoneal membrane than conventional solution. In addition, they permit better management of malnutrition and fluid status, and may thus help to improve PD patient survival. Although the effects of each of these new solutions have been well described, clinical documentation of the combined use of these new biocompatible PD solutions is still insufficient. However, the results of studies are expected, during the coming years, to support the combined use of the new solutions as the preferred standard practice for PD.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11229612

Source DB:  PubMed          Journal:  Perit Dial Int        ISSN: 0896-8608            Impact factor:   1.756


  7 in total

Review 1.  A peritoneal-based automated wearable artificial kidney.

Authors:  David B N Lee; Martin Roberts
Journal:  Clin Exp Nephrol       Date:  2008-04-03       Impact factor: 2.801

Review 2.  Icodextrin: a review of its use in peritoneal dialysis.

Authors:  James E Frampton; Greg L Plosker
Journal:  Drugs       Date:  2003       Impact factor: 9.546

3.  Neutral solution low in glucose degradation products is associated with less peritoneal fibrosis and vascular sclerosis in patients receiving peritoneal dialysis.

Authors:  Kunio Kawanishi; Kazuho Honda; Misao Tsukada; Hideaki Oda; Kosaku Nitta
Journal:  Perit Dial Int       Date:  2012-11-01       Impact factor: 1.756

Review 4.  Icodextrin and peritoneal dialysis: advantages and new applications.

Authors:  Periklis Dousdampanis; Carlos Guido Musso; Konstantina Trigka
Journal:  Int Urol Nephrol       Date:  2017-07-03       Impact factor: 2.370

5.  Regulation of complement C3 and C4 synthesis in human peritoneal mesothelial cells by peritoneal dialysis fluid.

Authors:  S Tang; J C K Leung; L Y Y Chan; A W L Tsang; C X R Chen; W Zhou; K N Lai; S H Sacks
Journal:  Clin Exp Immunol       Date:  2004-04       Impact factor: 4.330

Review 6.  Pathophysiology of the peritoneal membrane during peritoneal dialysis: the role of hyaluronan.

Authors:  Susan Yung; Tak Mao Chan
Journal:  J Biomed Biotechnol       Date:  2011-12-12

7.  Bimodal solutions or twice-daily icodextrin to enhance ultrafiltration in peritoneal dialysis patients.

Authors:  Periklis Dousdampanis; Konstantina Trigka; Joanne M Bargman
Journal:  Int J Nephrol       Date:  2013-01-08
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.