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      An isolated elevation in blood urea level is not ‘uraemia’ and not an indication for renal replacement therapy in the ICU

      editorial
      1 , 1 , 2 ,
      Critical Care
      BioMed Central
      Uraemia, RRT, ICU

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          Abstract

          The decision to initiate renal replacement therapy (RRT) and the optimal timing for commencement is a difficult decision faced by clinicians when treating acute kidney injury (AKI) in the intensive care setting. Without clinically significant ureamic symptoms or emergent indications (electrolyte abnormalities, volume overload) the timing of RRT initiation remains contentious and inconsistent across health providers. Current trends of initiating RRT in the ICU are often based on isolated blood urea levels without clear guidelines demonstrating an upper limit for treatment. Although the appropriate upper limit remains unclear, it is reasonable to conclude that a blood urea level less than 40 mmol/L is not in itself an indication for RRT, especially in the absence of supporting evidence of kidney impairment (anuria, elevated serum creatinine), presenting a welcome reminder to treat the patient and not a number.

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          Most cited references11

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          Effects of early high-volume continuous venovenous hemofiltration on survival and recovery of renal function in intensive care patients with acute renal failure: A prospective, randomized trial

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            Timing of renal replacement therapy and clinical outcomes in critically ill patients with severe acute kidney injury.

            The aim of this study is to evaluate the relationship between timing of renal replacement therapy (RRT) in severe acute kidney injury and clinical outcomes. This was a prospective multicenter observational study conducted at 54 intensive care units (ICUs) in 23 countries enrolling 1238 patients. Timing of RRT was stratified into "early" and "late" by median urea and creatinine at the time RRT was started. Timing was also categorized temporally from ICU admission into early ( 5 days). Renal replacement therapy timing by serum urea showed no significant difference in crude (63.4% for urea 24.2 mmol/L; odds ratio [OR], 0.92; 95% confidence interval [CI], 0.73-1.15; P = .48) or covariate-adjusted mortality (OR, 1.25; 95% CI, 0.91-1.70; P = .16). When stratified by creatinine, late RRT was associated with lower crude (53.4% for creatinine >309 micromol/L vs 71.4% for creatinine
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              Timing of initiation and discontinuation of renal replacement therapy in AKI: unanswered key questions.

              Patients with acute kidney injury (AKI) often require initiation of renal replacement therapy (RRT). Currently, there is wide variation worldwide on the indications for and timing of initiation and discontinuation of RRT for AKI. Various parameters for metabolic, solute, and fluid control are generally used to guide the initiation and discontinuation of therapy; however, there are currently no standards in this field. Members of the recently established Acute Kidney Injury Network, representing key societies in critical care and nephrology along with additional experts in adult and pediatric AKI, participated in a 3-d conference in Vancouver in September 2006 to evaluate the available literature on this topic and draft consensus recommendations for research studies in this area. Key questions included the following: what are the indications for RRT, when should acute RRT support be initiated, and when should RRT be stopped? This report summarizes the available evidence and describes in detail the key questions, and some of the methods of answering them that will need to be addressed with the goal of standardizing the care of patients with AKI and improving outcomes.
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                Author and article information

                Contributors
                Jack.Mackenzie@uon.edu.au
                Bobby.Chacko@hnehealth.nsw.gov.au
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                13 November 2017
                13 November 2017
                2017
                : 21
                : 275
                Affiliations
                [1 ]ISNI 0000 0000 8831 109X, GRID grid.266842.c, School of Medicine and Public Health, , University of Newcastle, ; Newcastle, NSW Australia
                [2 ]ISNI 0000 0004 0577 6676, GRID grid.414724.0, Nephrology and Transplantation Unit, John Hunter Hospital, ; Newcastle, NSW 2310 Australia
                Author information
                http://orcid.org/0000-0002-0292-5512
                Article
                1868
                10.1186/s13054-017-1868-x
                5683443
                29132411
                e3761a76-c5fc-4bc2-b8d9-7735d403e953
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 6 October 2017
                : 23 October 2017
                Categories
                Editorial
                Custom metadata
                © The Author(s) 2017

                Emergency medicine & Trauma
                uraemia,rrt,icu
                Emergency medicine & Trauma
                uraemia, rrt, icu

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