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      Bioimpedance Analysis in Dialysis: State of the Art and What We Can Expect

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          Abstract

          Dialysis must control the body’s fluid content accurately in order to maintain optimal health. The only commonly used, practical and objective measurements we have to guide fluid removal are very inaccurate. Recent study has validated bioimpedance (BIA) as an objective measure of fluid and nutritional status in dialysis patients. There are a number of different methods suitable for routine use available to the clinician. Single-frequency whole-body BIA uses inexpensive equipment capable of almost instantaneous or continuous measurement. The results can be used to give an indication of a patient’s fluid content, nutrition and body composition when compared to appropriate reference values. Multiple-frequency whole-body BIA can be used to calculate excess fluid volume to within 1–2 liters. The equipment is more expensive than for single-frequency BIA, but the output is much easier to interpret. Multiple-frequency segmental BIA is more complicated to perform, but subject to less interference from changes in fluid distribution (e.g. resulting from hemodialysis or changes in posture). It is not suitable for routine use but could be considered as a gold standard for occasional clinical BIA.

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          Theory of the dielectric dispersion due to the interfacial polarization and its application to emulsions

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            Bioelectric impedance vector distribution in peritoneal dialysis patients with different hydration status.

            In continuous ambulatory peritoneal dialysis (CAPD), total body water (TBW) is estimated by functions of body weight, and by equations of bioelectric impedance analysis (BIA). These procedures may be biased with abnormal tissue hydration. We validated vector BIA (BIVA) patterns of hydration in CAPD patients, based on direct measurements of resistance (R) and reactance (Xc) (RXc graph) without knowledge of the body weight. Cross-sectional study in 200 adult CAPD patients from two groups: 149 patients (77 males and 72 females) without edema (BMI 24.3 kg/m2), and 51 (29 males and 22 females) with pitting edema (BMI 24.6 kg/m2). Single frequency (50 kHz), whole-body impedance vector was measured with both empty and filled peritoneal cavity. Vector distribution was compared with that from 726 healthy subjects, 1116 hemodialysis patients, and 50 nephrotic patients, all with a same BMI. The performance of BIVA was compared with indications of four anthropometry and four conventional BIA equations for TBW. TBW estimates from anthropometry (Watson, Hume and Weyers, Chertow, and Johansson formulas) were misleading, indicating the same hydration in edema. TBW estimates from BIA equations indicated a 10% excess TBW in edema. BIVA were very sensitive to fluid overload, as both R (by 10%) and Xc (by 40%) were reduced in patients with edema (regardless of peritoneal filling). The vector distribution of individual CAPD patients without edema was superposable to that of the healthy, gender-specific, reference population (50%, 75%, and 95% tolerance ellipses, RXc graph) and close to the hemodialysis, presession distribution. Vectors from patients with edema were displaced downward on the RXc graph, out of the 75% ellipse (88% sensitivity and 87% specificity), and close to vectors from nephrotic patients. CAPD prescription would keep or bring vectors of patients back into the 75% reference ellipse (border for progression from latent to apparent overhydration across the lower pole) regardless of body weight. Whether CAPD patients with vector within the target ellipse have better outcome needs longitudinal evaluation.
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              Vector length as a proxy for the adequacy of ultrafiltration in hemodialysis.

              Evaluation of dialysis adequacy has focused on parameters of solute (principally urea) clearance. Relatively little attention has been paid to the adequacy of ultrafiltration. At a given phase angle, the bioimpedance vector length reflects the degree of tissue hydration, as the vector lengthens with ultrafiltration. We determined the relative risk of death associated with different bioimpedance vector lengths in a 3009 patient hemodialysis cohort using proportional hazards regression. The mean phase angle was 4.8 degrees, and the mean vector length 300 +/- 70 ohm/m (range 140 to 630 ohm/m). Vector length was much longer in women than men (mean 340 vs. 270 ohm/m) and significantly longer in African Americans and patients without diabetes. Adjusted for the effects of age, gender, race, diabetes, vintage, weight, albumin, prealbumin, creatinine, hemoglobin, ferritin, and dialysis dose, the relative risk (RR) of death was 0.75 (95% CI 0.57 to 0.88) per 100 ohm/m decrease in vector length. The effect of vector length on RR was somewhat more pronounced among men (vector length x gender interaction, P= 0.07). Considering vector length of 300 to 350 ohm/m as the referent category, the RRs of death were 1.54 (95% CI 1.08 to 2.21) and 2.83 (95% CI 1.55 to 5.14) for patients with vector length 200 to 250 and <200 ohm/m, respectively. Shorter predialysis bioimpedance vectors, indicating greater soft tissue hydration, were associated with diminished survival in hemodialysis patients. These findings validate clinical observations linking longevity to maintenance of dry body weight.
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                Author and article information

                Journal
                BPU
                Blood Purif
                10.1159/issn.0253-5068
                Blood Purification
                S. Karger AG
                978-3-8055-9031-0
                978-3-8055-9032-7
                0253-5068
                1421-9735
                2009
                January 2009
                23 January 2009
                : 27
                : 1
                : 70-74
                Affiliations
                Leeds Teaching Hospitals, Leeds, UK
                Article
                167012 Blood Purif 2009;27:70–74
                10.1159/000167012
                19169021
                adc2f719-3cff-4b0c-a995-cded5b128fd9
                © 2009 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
                Page count
                Tables: 1, References: 17, Pages: 5
                Categories
                Paper

                Cardiovascular Medicine,Nephrology
                Single-frequency whole-body bioimpedance,Multiple-frequency whole-body bioimpedance,Multiple-frequency segmental bioimpedance,Dialysis

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