Literature DB >> 15947984

Zero balance ultrafiltration (Z-BUF) in blood-primed CRRT circuits achieves electrolyte and acid-base homeostasis prior to patient connection.

Richard M Hackbarth1, Dawn Eding, Carla Gianoli Smith, Ada Koch, Dominic J Sanfilippo, Timothy E Bunchman.   

Abstract

Infants requiring CRRT present a unique challenge due to the large circuit volume to blood volume ratio. Blood priming is often used, but some patients can become unstable during the initiation of CRRT due to electrolyte and acid-base imbalance. We postulated that using Z-BUF we could normalize electrolytes and improve the acid base status of the prime prior to patient connection. To test this we set up a circuit using the Baxter BM-25 CRRT pump, a polysulfone or AN-69 membrane, and a three-way stopcock. The circuit was primed with a 60/40 mix of expired autologous donor pRBCs and 5% albumin. The modalities of CVVH, CVVHD, and CVVHDF were compared for relative efficacy. Electrolytes, lactate, pH, cytokines (TNF-alpha, IL-1beta, bradykinin, and IL-6) were measured. Plasma hemoglobin levels were also measured before and after the Z-BUF procedure. Bradykinin production and elimination in AN-69 membrane circuits were assessed. All lab values equilibrated by 35 minutes. All CRRT modalities were equally efficacious for Z-BUF. Cytokine production or significant hemolysis was not found. In addition, no bradykinin accumulation occurred in AN-69 membrane-containing circuits. We conclude that Z-BUF is a simple and effective way to normalize electrolyte and acid-base status in the CRRT circuit when blood priming is required.

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Year:  2005        PMID: 15947984     DOI: 10.1007/s00467-005-1970-1

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  11 in total

1.  AN-69 membrane reactions are pH-dependent and preventable.

Authors:  P D Brophy; T A Mottes; T L Kudelka; K D McBryde; J J Gardner; N J Maxvold; T E Bunchman
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2.  Generation of cytokines in red cell concentrates during storage is prevented by prestorage white cell reduction.

Authors:  A Shanwell; M Kristiansson; M Remberger; O Ringdén
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Review 4.  Mediator removal with CRRT: complement and cytokines.

Authors:  W Silvester
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5.  Cytokine kinetics (TNF-alpha, IL-1 beta, IL-6) during continuous hemofiltration: a laboratory and clinical study.

Authors:  E F van Bommel; C J Hesse; N H Jutte; R Zietse; H A Bruining; W Weimar
Journal:  Contrib Nephrol       Date:  1995       Impact factor: 1.580

6.  Cytokine generation in whole blood, leukocyte-depleted and temporarily warmed red blood cell concentrates.

Authors:  V Weisbach; C Wanke; J Zingsem; R Zimmermann; R Eckstein
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7.  Neonatal hyperkalemic-hypocalcemic cardiac arrest associated with initiation of blood-primed continuous venovenous hemofiltration.

Authors:  Christopher S Parshuram; Peter N Cox
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8.  High-volume, zero-balanced hemofiltration to reduce delayed inflammatory response to cardiopulmonary bypass in children.

Authors:  D Journois; D Israel-Biet; P Pouard; B Rolland; W Silvester; P Vouhé; D Safran
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9.  Cytokine filtration and adsorption during pre- and postdilution hemofiltration in four different membranes.

Authors:  C S Bouman; R W van Olden; C P Stoutenbeek
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Authors:  Deborah A Pasko; Theresa A Mottes; Bruce A Mueller
Journal:  Pediatr Nephrol       Date:  2003-10-02       Impact factor: 3.714

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Review 5.  Pediatric renal replacement therapy in the intensive care unit.

Authors:  Brian C Bridges; David J Askenazi; Jessimene Smith; Stuart L Goldstein
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6.  Serial measurement of electrolyte and citrate concentrations in blood-primed continuous hemodialysis circuits during closed-circuit dialysis.

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8.  Use of HF20 membrane in critically ill unstable low-body-weight infants on inotropic support.

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9.  Ability of a novel system for neonatal extracorporeal renal replacement therapy with an ultra-small volume circuit to remove solutes in vitro.

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10.  Section 5: Dialysis Interventions for Treatment of AKI.

Authors: 
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