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The clinical usefulness of peritoneal dialysis fluids with neutral pH and low glucose degradation product concentration: an open randomized prospective trial

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dc.contributor.author한승혁-
dc.contributor.author김동기-
dc.contributor.author김범석-
dc.contributor.author문성진-
dc.contributor.author박형천-
dc.contributor.author이정은-
dc.contributor.author이태희-
dc.contributor.author이호영-
dc.contributor.author최규헌-
dc.contributor.author최훈영-
dc.contributor.author하성규-
dc.contributor.author한대석-
dc.date.accessioned2015-05-19T16:27:52Z-
dc.date.available2015-05-19T16:27:52Z-
dc.date.issued2008-
dc.identifier.issn0896-8608-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/106354-
dc.description.abstractBACKGROUND: Long-term peritoneal dialysis (PD) is associated with the development of various structural and functional changes to the peritoneal membrane when bioincompatible conventional peritoneal dialysis fluids (PDFs) are used. In this study, we looked at patients that were treated with conventional PDFs and then changed to novel biocompatible PDFs with a neutral pH and a low concentration of glucose degradation products (GDPs) to investigate whether this change could result in the arrest or reversal of peritoneal membrane deterioration. METHODS: In an open label, randomized prospective trial, the clinical effects of conventional PDFs and biocompatible PDFs with neutral pH and very low concentration of GDPs were compared in 104 patients equally divided between both study PDFs. Blood and effluent dialysate samples, peritoneal equilibration tests, and adequacy evaluation were undertaken at baseline, 4, 8, and 12 months. The target variables were the ratio of dialysate-to-plasma (D/P) creatinine, peritoneal ultrafiltration, residual renal function, dialysis adequacy indices, and effluent cancer antigen 125 (CA125). RESULTS: D/P creatinine values were not different in the two groups. Peritoneal ultrafiltration was significantly higher in the low-GDP PDF group than in the conventional PDF group at all follow-up times (4 months: 9.1 +/- 4.3 vs 6.0 +/- 3.0; 8 months: 8.3 +/- 3.4 vs 6.0 +/- 3.0; 12 months: 8.9 +/- 3.3 vs 6.1 +/- 3.3 mL/g dextrose/day; p < 0.05). Peritoneal Kt/V urea values and total weekly Kt/V urea values at 4 months were significantly higher in the low-GDP PDF group than in the conventional PDF group. Residual renal function was not statistically significant. Effluent CA125 levels were significantly higher in the low-GDP PDF group at all follow-up visits (4 months: 37.8 +/- 20.8 vs 22.0 +/- 9.5; 8 months: 41.2 +/- 20.3 vs 25.9 +/- 11.3; 12 months: 40.4 +/- 21.4 vs 28.6 +/- 13.0 U/mL; p < 0.05). Among anuric patients, peritoneal ultrafiltration at 4, 8, and 12 months, total weekly Kt/V at 4 and 8 months, and CA125 levels at all follow-up visits were significantly higher in patients treated with low-GDP PDF than those treated with conventional PDF. However, among anuric patients, D/P creatinine showed no significant differences between the low-GDP PDF group and the conventional PDF group. CONCLUSION: The use of biocompatible PDFs with neutral pH and low GDP concentration can contribute to improvement of peritoneal ultrafiltration and peritoneal effluent CA125 level, an indicator of peritoneal membrane integrity in PD patients-
dc.description.statementOfResponsibilityopen-
dc.format.extent174~182-
dc.relation.isPartOfPERITONEAL DIALYSIS INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnuria/physiopathology-
dc.subject.MESHBiocompatible Materials-
dc.subject.MESHCA-125 Antigen/analysis-
dc.subject.MESHCreatinine/analysis-
dc.subject.MESHFemale-
dc.subject.MESHGlucose/analysis*-
dc.subject.MESHHemodialysis Solutions/chemistry*-
dc.subject.MESHHumans-
dc.subject.MESHHydrogen-Ion Concentration-
dc.subject.MESHKidney/physiopathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPeritoneal Dialysis*-
dc.subject.MESHPeritoneum/metabolism-
dc.subject.MESHUrea/analysis-
dc.titleThe clinical usefulness of peritoneal dialysis fluids with neutral pH and low glucose degradation product concentration: an open randomized prospective trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorHoon Young Choi-
dc.contributor.googleauthorDong Ki Kim-
dc.contributor.googleauthorTae Hee Lee-
dc.contributor.googleauthorSung Jin Moon-
dc.contributor.googleauthorSeung Hyeok Han-
dc.contributor.googleauthorJung Eun Lee-
dc.contributor.googleauthorBeom Seok Kim-
dc.contributor.googleauthorHyeong Cheon Park-
dc.contributor.googleauthorKyu Hun Choi-
dc.contributor.googleauthorSung Kyu Ha-
dc.contributor.googleauthorDae-Suk Han-
dc.contributor.googleauthorHo Yung Lee-
dc.identifier.doi18332454-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA04304-
dc.contributor.localIdA00488-
dc.contributor.localIdA01364-
dc.contributor.localIdA01759-
dc.contributor.localIdA03266-
dc.contributor.localIdA03326-
dc.contributor.localIdA04043-
dc.contributor.localIdA04226-
dc.contributor.localIdA04252-
dc.contributor.localIdA04272-
dc.contributor.localIdA03119-
dc.contributor.localIdA00400-
dc.relation.journalcodeJ02500-
dc.identifier.eissn1718-4304-
dc.identifier.pmid18332454-
dc.subject.keywordGlucose degradation products-
dc.subject.keywordneutral pH-
dc.subject.keywordbiocompatibility-
dc.subject.keywordperitoneal function-
dc.subject.keywordCA125-
dc.contributor.alternativeNameHan, Seung Hyeok-
dc.contributor.alternativeNameKim, Dong Ki-
dc.contributor.alternativeNameKim, Beom Seok-
dc.contributor.alternativeNameMoon, Sung Jin-
dc.contributor.alternativeNamePark, Hyeong Cheon-
dc.contributor.alternativeNameLee, Jung Eun-
dc.contributor.alternativeNameLee, Tae Hee-
dc.contributor.alternativeNameLee, Ho Yung-
dc.contributor.alternativeNameChoi, Kyu Hun-
dc.contributor.alternativeNameChoi, Hoon Young-
dc.contributor.alternativeNameHa, Sung Kyu-
dc.contributor.alternativeNameHan, Dae Suk-
dc.contributor.affiliatedAuthorHan, Seung Hyeok-
dc.contributor.affiliatedAuthorKim, Beom Seok-
dc.contributor.affiliatedAuthorMoon, Sung Jin-
dc.contributor.affiliatedAuthorPark, Hyeong Cheon-
dc.contributor.affiliatedAuthorLee, Tae Hee-
dc.contributor.affiliatedAuthorLee, Ho Yung-
dc.contributor.affiliatedAuthorChoi, Kyu Hun-
dc.contributor.affiliatedAuthorChoi, Hoon Young-
dc.contributor.affiliatedAuthorHa, Sung Kyu-
dc.contributor.affiliatedAuthorHan, Dae Suk-
dc.contributor.affiliatedAuthorLee, Jung Eun-
dc.contributor.affiliatedAuthorKim, Dong Ki-
dc.rights.accessRightsfree-
dc.citation.volume28-
dc.citation.number2-
dc.citation.startPage174-
dc.citation.endPage182-
dc.identifier.bibliographicCitationPERITONEAL DIALYSIS INTERNATIONAL, Vol.28(2) : 174-182, 2008-
dc.identifier.rimsid44371-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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