1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Measured GFR in Routine Clinical Practice – The Promise of Dried Blood Spots

      research-article
      , M.D. 1 , 2 , , M.D., Ph.D. 3 , , M.D., Ph.D. 4
      Advances in chronic kidney disease

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Accurate determination of GFR is crucial for the diagnosis of kidney disease. Estimated GFR (eGFR) calculated by serum creatinine and/or cystatin C is a mainstay in clinical practice and epidemiologic research, but lacks precision and accuracy until GFR <60ml/min/1.73m 2. Furthermore, eGFR may not precisely and accurately represent changes in GFR longitudinally. The lack of precision and accuracy is of concern in populations at high risk for kidney disease, as the dissociation between changes in eGFR and GFR may lead to missed diagnoses of early kidney disease. Therefore, improved methods to quantify GFR are needed. Whereas direct measures of GFR have been too cumbersome for screening and ambulatory care, a practical method of measuring GFR by iohexol clearance using dried capillary blood spots (DBS) exists. In this review, we examine the current literature and data addressing GFR measurements by DBS, and its potential application in high-risk groups.

          Related collections

          Author and article information

          Journal
          101209214
          31964
          Adv Chronic Kidney Dis
          Adv Chronic Kidney Dis
          Advances in chronic kidney disease
          1548-5595
          1548-5609
          28 September 2017
          January 2018
          01 January 2019
          : 25
          : 1
          : 76-83
          Affiliations
          [1 ]Department of Pediatric Endocrinology, University of Colorado School of Medicine, Aurora, CO
          [2 ]Barbara Davis Center for Diabetes, University of Colorado Denver, Aurora, CO
          [3 ]Department of Laboratory Medicine and Pathology, University of Minnesota School of Medicine, Minneapolis, MN
          [4 ]Department of Pediatric Endocrinology, Stanford University School of Medicine, Palo Alto, CA
          Author notes
          Address all correspondence to: Petter Bjornstad, M.D., Barbara Davis Center for Childhood Diabetes, University of Colorado, Denver, 1775 Aurora Court, Aurora, CO 80045, Phone: 720.579.1048, Fax: 303.724.6779, Petter.Bjornstad@ 123456childrenscolorado.org
          Article
          PMC5836491 PMC5836491 5836491 nihpa908848
          10.1053/j.ackd.2017.09.003
          5836491
          29499891
          4df3c629-ff8b-4f8a-b007-91d959f1e3a8
          History
          Categories
          Article

          Comments

          Comment on this article