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      Fractional Solute Removal and KT/V in Different Modalities of Renal Replacement Therapy

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          Abstract

          The efficacy of solute removal by renal replacement therapy can be assessed by the commonly used index of KT/V (the fraction of the volume cleared from a solute). Fractional solute removal (FSR, the fraction of the total amount of the solute that was removed) is an alternative index that may be more appropriate than KT/V for comparison of the efficacy of different treatment modalities. To elucidate the relationship between these two indexes, we propose to discriminate between two notions of clearance: (1) instantaneous clearance K = (solute removal rate)/C<sub>B</sub>, where C<sub>B</sub> is solute concentration in blood, and (2) treatment clearance K<sub>T</sub> = (average rate of solute removal per treatment)/C<sub>B0</sub>, where C<sub>B0</sub> is C<sub>B</sub> at the beginning of the treatment. K is the clearance of the purification device (glomeruli, hemodialyzer or hemofilter) and the diffusive mass transport parameter (K<sub>BD</sub>, MTAC) for continuous ambulatory peritoneal dialysis (CAPD). For all modalities of renal replacement therapy: FSR = K<sub>T</sub>T/V, and K<sub>T</sub> generally decreases with the treatment time. For purification of a single compartment with a constant volume, V, using an open loop system (i.e. with no recirculation or dwelling of dialysis fluid, as in hemodialysis (HD), hemofiltration (HF) or in the native kidney), FSR is a function of only one lumped, nondimensional parameter, KT/V<sub>B</sub>, where V<sub>B</sub> is the distribution volume of the solute within the body. In contrast, if closed loop systems are applied, as for example in HD with recirculation of dialysis fluid (RD) or in peritoneal dialysis, FSR depends on two lumped, nondimensional parameters: KT/V<sub>B</sub> and KT/V<sub>D</sub>, where V<sub>D</sub> is the volume of dialysis fluid. It is necessary to discriminate between K and K<sub>T</sub> for analysis of dialysis dose. For HD and HF, FSR is a function of KT/V, whereas KT/V alone does not allow calculation of FSR for CAPD and RD. The current practice of using K<sub>T</sub>T/V for CAPD but KT/V for HD and HF leads to confusion because of the inconsistency in the interpretation of the quantitative prescription of dialysis dose. The application of FSR, instead of KT/V, for all treatment modalities may solve this dilemma. Furthermore, K<sub>T</sub>T/V (currently used only for CAPD) is equal to FSR for all treatment modalities. Both FSR and K<sub>T</sub> may be generalized to describe the total solute removal per treatment cycle composed from a few treatment sessions. A few different definitions of the adequacy parameters for the treatment cycle are formulated and discussed.

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          Most cited references14

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          Kt/V Is the Best Dialysis Dose Parameter

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            Quantification of middle molecular weight solute removal in dialysis.

            The pioneering work of Gotch emphasized the critical need to be quantitative with respect to treatment prescription. Through his meticulous derivations and analyses regarding Kt/V(urea), he has provided powerful insight into the standard therapy prescriptions that we now employ clinically. However, time has seen the proliferation of treatment techniques, most of which are too "young" to have been characterized with respect to clinical outcomes. Further, the relationship between removal of urea and removal of middle molecular size solutes associated with these newer techniques deviates from that associated with conventional, clinically qualified techniques. In this article we examine the solute clearance profile of some of these new methodologies and their relationship to current criteria for treatment adequacy. Our approach is to discuss components of the overall transport process and then utilize modeling of surrogate molecules over the size range of interest whose transport characteristics are known. Alteration in the solute clearance profile of these surrogate markers in response to changes in prescription variables will thus offer insight into the spectrum of toxic middle molecules that are removed when size, space of distribution, and generation rate are known.
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              Whither goest Kt/V?

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                Author and article information

                Journal
                BPU
                Blood Purif
                10.1159/issn.0253-5068
                Blood Purification
                S. Karger AG
                0253-5068
                1421-9735
                2004
                June 2004
                02 September 2004
                : 22
                : 4
                : 367-376
                Affiliations
                aDivisions of Baxter Novum and Renal Medicine, Karolinska Institute, Stockholm, Sweden, and bInstitute of Biocybernetics and Biomedical Engineering, Warsaw, Poland
                Article
                80033 Blood Purif 2004;22:367–376
                10.1159/000080033
                15297787
                fcebaf74-9e53-477b-84a4-3d2d0480a31e
                © 2004 S. Karger AG, Basel

                Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

                History
                : 09 July 2003
                : 30 April 2004
                Page count
                Figures: 2, Tables: 4, References: 22, Pages: 10
                Categories
                Review Article

                Cardiovascular Medicine,Nephrology
                Adequacy,Mathematical model,Hemodialysis,Peritoneal dialysis,Urea removal,Renal replacement therapy

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