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Prognostic Value of Residual Urine Volume, GFR by 24-hour Urine Collection, and eGFR in Patients Receiving Dialysis

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dc.contributor.author강신욱-
dc.contributor.author권영은-
dc.contributor.author박정탁-
dc.contributor.author유태현-
dc.contributor.author한승혁-
dc.date.accessioned2017-11-02T08:28:44Z-
dc.date.available2017-11-02T08:28:44Z-
dc.date.issued2017-
dc.identifier.issn1555-9041-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/154512-
dc.description.abstractBACKGROUND AND OBJECTIVES: Residual kidney function can be assessed by simply measuring urine volume, calculating GFR using 24-hour urine collection, or estimating GFR using the proposed equation (eGFR). We aimed to investigate the relative prognostic value of these residual kidney function parameters in patients on dialysis. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Using the database from a nationwide prospective cohort study, we compared differential implications of the residual kidney function indices in 1946 patients on dialysis at 36 dialysis centers in Korea between August 1, 2008 and December 31, 2014. Residual GFR calculated using 24-hour urine collection was determined by an average of renal urea and creatinine clearance on the basis of 24-hour urine collection. eGFR-urea, creatinine and eGFR β2-microglobulin were calculated from the equations using serum urea and creatinine and β2-microglobulin, respectively. The primary outcome was all-cause death. RESULTS: During a mean follow-up of 42 months, 385 (19.8%) patients died. In multivariable Cox analyses, residual urine volume (hazard ratio, 0.96 per 0.1-L/d higher volume; 95% confidence interval, 0.94 to 0.98) and GFR calculated using 24-hour urine collection (hazard ratio, 0.98; 95% confidence interval, 0.95 to 0.99) were independently associated with all-cause mortality. In 1640 patients who had eGFR β2-microglobulin data, eGFR β2-microglobulin (hazard ratio, 0.98; 95% confidence interval, 0.96 to 0.99) was also significantly associated with all-cause mortality as well as residual urine volume (hazard ratio, 0.96 per 0.1-L/d higher volume; 95% confidence interval, 0.94 to 0.98) and GFR calculated using 24-hour urine collection (hazard ratio, 0.97; 95% confidence interval, 0.95 to 0.99). When each residual kidney function index was added to the base model, only urine volume improved the predictability for all-cause mortality (net reclassification index =0.11, P=0.01; integrated discrimination improvement =0.01, P=0.01). CONCLUSIONS: Higher residual urine volume was significantly associated with a lower risk of death and exhibited a stronger association with mortality than GFR calculated using 24-hour urine collection and eGFR-urea, creatinine. These results suggest that determining residual urine volume may be beneficial to predict patient survival in patients on dialysis.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherAmerican Society of Nephrology-
dc.relation.isPartOfCLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHCreatinine/blood-
dc.subject.MESHFemale-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHGlomerular Filtration Rate*-
dc.subject.MESHHumans-
dc.subject.MESHKidney Failure, Chronic/physiopathology*-
dc.subject.MESHKidney Failure, Chronic/therapy*-
dc.subject.MESHKidney Failure, Chronic/urine-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHPrognosis-
dc.subject.MESHProspective Studies-
dc.subject.MESHRenal Dialysis-
dc.subject.MESHSurvival Rate-
dc.subject.MESHUrea/blood-
dc.subject.MESHUrine-
dc.subject.MESHbeta 2-Microglobulin/blood-
dc.titlePrognostic Value of Residual Urine Volume, GFR by 24-hour Urine Collection, and eGFR in Patients Receiving Dialysis-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorMi Jung Lee-
dc.contributor.googleauthorJung Tak Park-
dc.contributor.googleauthorKyoung Sook Park-
dc.contributor.googleauthorYoung Eun Kwon-
dc.contributor.googleauthorHyung Jung Oh-
dc.contributor.googleauthorTae-Hyun Yoo-
dc.contributor.googleauthorYong-Lim Kim-
dc.contributor.googleauthorYon Su Kim-
dc.contributor.googleauthorChul Woo Yang-
dc.contributor.googleauthorNam-Ho Kim-
dc.contributor.googleauthorShin-Wook Kang-
dc.contributor.googleauthorSeung Hyeok Han-
dc.identifier.doi10.2215/CJN.05520516-
dc.contributor.localIdA00232-
dc.contributor.localIdA01654-
dc.contributor.localIdA02526-
dc.contributor.localIdA04304-
dc.contributor.localIdA00053-
dc.relation.journalcodeJ00584-
dc.identifier.eissn1555-905X-
dc.identifier.pmid28228465-
dc.identifier.urlhttp://cjasn.asnjournals.org/content/12/3/426.long-
dc.subject.keyworddialysis-
dc.subject.keywordend-stage renal disease-
dc.subject.keywordglomerular filtration rate-
dc.subject.keywordmortality-
dc.subject.keywordresidual kidney function-
dc.subject.keywordurine volume-
dc.contributor.alternativeNameKang, Shin Wook-
dc.contributor.alternativeNameKwon, Young Eun-
dc.contributor.alternativeNamePark, Jung Tak-
dc.contributor.alternativeNameYoo, Tae Hyun-
dc.contributor.alternativeNameHan, Seung Hyeok-
dc.contributor.affiliatedAuthorKwon, Young Eun-
dc.contributor.affiliatedAuthorPark, Jung Tak-
dc.contributor.affiliatedAuthorYoo, Tae Hyun-
dc.contributor.affiliatedAuthorHan, Seung Hyeok-
dc.contributor.affiliatedAuthorKang, Shin Wook-
dc.citation.titleClinical Journal of the American Society of Nephrology-
dc.citation.volume12-
dc.citation.number3-
dc.citation.startPage426-
dc.citation.endPage434-
dc.identifier.bibliographicCitationCLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, Vol.12(3) : 426-434, 2017-
dc.date.modified2017-11-01-
dc.identifier.rimsid43560-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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