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Comparison of icodextrin and 2.5% glucose in potassium metabolism by acute K+ load via dialysate in continuous ambulatory peritoneal dialysis patients

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dc.contributor.authorYi, Joo-Hark-
dc.contributor.authorYun, Yeo-Wook-
dc.contributor.authorHan, Sang Woong-
dc.contributor.authorKim, Ho-Jung-
dc.date.accessioned2022-12-20T21:51:17Z-
dc.date.available2022-12-20T21:51:17Z-
dc.date.created2022-09-16-
dc.date.issued2009-06-
dc.identifier.issn1738-5997-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/176645-
dc.description.abstractThis study aimed to compare the increment in plasma potassium concentration ([K+]) as well as the role of internal K+ balance for its changes following acute K+ supplementation between conventional 2.5% glucose (GD) and non-glucose containing dialysate (icodextrin, ID) in continuous ambulatory peritoneal dialysis (CAPD) patients. A total of 9 stable CAPD patients (5 men and 4 women; age, 56±13 years; 7 type-2 diabetics and 2 non-diabetics) on daily 4 exchanges of 2 L of glucose dialysate underwent the 6-hr dwell on fasting in the morning with 2 L of 2.5% glucose mixed with 20 mEq/L of KCl, and then the same regimen was repeated with icodextrin after 1-wk interval. The degree of intraperitoneal absorption was comparable, 65±2% in GD and 68+2% in ID, respectively (p=NS). However, despite the similar plasma K+ levels at the baseline of both regimens, its increment was significantly less in GD than ID, which was accompanied by more marked increase in the calculated intracellular K+ redistribution (68±3% vs. 52±3%, p<0.05). The basal levels of insulin were similar between the GD and ID groups. However, the change, checked up after 2 hours' dwell, from the basal insulin levels was much lower on ID. ID with a lesser degree of transcelluar K+ shift by the decreased secretion of insulin is more effective than the conventional glucose solution for acute K+ repletion via dialysate during CAPD. Furthermore, these results suggested that the role of insulin for the internal K+ balance was intact even in type-2 diabetic patients on CAPD.-
dc.language영어-
dc.language.isoen-
dc.publisherKorean Society of Electrolyte and Blood Pressure Research-
dc.titleComparison of icodextrin and 2.5% glucose in potassium metabolism by acute K+ load via dialysate in continuous ambulatory peritoneal dialysis patients-
dc.typeArticle-
dc.contributor.affiliatedAuthorHan, Sang Woong-
dc.identifier.doi10.5049/EBP.2009.7.1.25-
dc.identifier.scopusid2-s2.0-76549113314-
dc.identifier.bibliographicCitationElectrolyte and Blood Pressure, v.7, no.1, pp.25 - 30-
dc.relation.isPartOfElectrolyte and Blood Pressure-
dc.citation.titleElectrolyte and Blood Pressure-
dc.citation.volume7-
dc.citation.number1-
dc.citation.startPage25-
dc.citation.endPage30-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001347797-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.description.journalRegisteredClassother-
dc.subject.keywordPlusglucose-
dc.subject.keywordPlusicodextrin-
dc.subject.keywordPlusinsulin-
dc.subject.keywordPluspotassium-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusarticle-
dc.subject.keywordPluschronic glomerulonephritis-
dc.subject.keywordPlusclinical article-
dc.subject.keywordPluscontinuous ambulatory peritoneal dialysis-
dc.subject.keywordPlusdialysate-
dc.subject.keywordPlusdiet restriction-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlushuman-
dc.subject.keywordPlushypokalemia-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusnon insulin dependent diabetes mellitus-
dc.subject.keywordPluspotassium balance-
dc.subject.keywordPluspotassium blood level-
dc.subject.keywordPluspotassium cell level-
dc.subject.keywordPluspotassium metabolism-
dc.subject.keywordPlussupplementation-
dc.subject.keywordAuthorContinuous ambulatory-
dc.subject.keywordAuthorHypokalemia-
dc.subject.keywordAuthorIcodextrin-
dc.subject.keywordAuthorPeritoneal dialysis-
dc.subject.keywordAuthorPotassium supplementation-
dc.identifier.urlhttps://enbpr.org/DOIx.php?id=10.5049/EBP.2009.7.1.25-
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