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      Accelerated versus standard initiation of renal replacement therapy for critically ill patients with acute kidney injury: a systematic review and meta-analysis of RCT studies

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          Abstract

          Background

          Acute kidney injury (AKI) is a common yet possibly fatal complication among critically ill patients in intensive care units (ICU). Although renal replacement therapy (RRT) is an important supportive management for severe AKI patients, the optimal timing of RRT initiation for these patients is still unclear.

          Methods

          In this systematic review, we searched all relevant randomized controlled trials (RCTs) that directly compared accelerated with standard initiation of RRT from PUBMED, MEDLINE, EMBASE, and Cnki.net published prior to July, 20, 2020. We extracted study characteristics and outcomes of being free of dialysis, dialysis dependence and mortality. We rated the certainty of evidence according to Cochrane methods and the GRADE approach.

          Results

          We identified 56 published relevant studies from 1071 screened abstracts. Ten RCTs with 4753 critically ill AKI patients in intensive care unit (ICU) were included in this meta-analysis. In our study, accelerated and standard RRT group were not associated with all-cause mortality (log odds-ratio [OR]: − 0.04, 95% confidence intervals [CI] − 0.16 to 0.07, p = 0.46) and free of dialysis (log OR: − 0.03, 95% CI − 0.14 to 0.09, p = 0.65). In the subgroup analyses, accelerated RRT group was significantly associated with lower risk of all-cause mortality in the surgical ICU and for those who received continuous renal replacement therapy (CRRT). In addition, patients in these two subgroups had higher chances of being eventually dialysis-free. However, accelerated initiation of RRT augmented the risk of dialysis dependence in the subgroups of patients treated with non-CRRT modality and whose Sequential Organ Failure Assessment (SOFA) score were more than 11.

          Conclusions

          In this meta-analysis, critically ill patients with severe AKI would benefit from accelerated RRT initiation regarding all-cause mortality and being eventually free of dialysis only if they were surgical ICU patients or if they underwent CRRT treatment. However, the risk of dialysis dependence was increased in the accelerated RRT group when those patients used non-CRRT modality or had high SOFA scores. All the literatures reviewed in this study were highly heterogeneous and potentially subject to biases.

          Trial registration CRD42020201466, Sep 07, 2020. https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=201466.

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          Most cited references32

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          Measuring inconsistency in meta-analyses.

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            The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials

            Flaws in the design, conduct, analysis, and reporting of randomised trials can cause the effect of an intervention to be underestimated or overestimated. The Cochrane Collaboration’s tool for assessing risk of bias aims to make the process clearer and more accurate
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              Updated guidance for trusted systematic reviews: a new edition of the Cochrane Handbook for Systematic Reviews of Interventions

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                Author and article information

                Contributors
                q91421028@ntu.edu.tw
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                5 January 2021
                5 January 2021
                2021
                : 25
                : 5
                Affiliations
                [1 ]GRID grid.454209.e, ISNI 0000 0004 0639 2551, Division of Nephrology, Department of Internal Medicine, , Keelung Chang Gung Memorial Hospital, ; Keelung, Taiwan
                [2 ]GRID grid.19188.39, ISNI 0000 0004 0546 0241, Graduate Institute of Clinical Medicine, College of Medicine, , National Taiwan University, ; Taipei, Taiwan
                [3 ]GRID grid.145695.a, Chang Gung University College of Medicine, ; Taoyuan, Taiwan
                [4 ]GRID grid.454209.e, ISNI 0000 0004 0639 2551, Community Medicine Research Center, , Keelung Chang Gung Memorial Hospital, ; Keelung, Taiwan
                [5 ]GRID grid.413593.9, ISNI 0000 0004 0573 007X, Division of Nephrology, Department of Internal Medicine, , MacKay Memorial Hospital, ; Taipei, Taiwan
                [6 ]GRID grid.19188.39, ISNI 0000 0004 0546 0241, Division of Nephrology, Department of Pediatrics, , National Taiwan University Children’s Hospital, ; Taipei, Taiwan
                [7 ]GRID grid.459908.9, Division of Nephrology, Department of Internal Medicine, , Saint Mary’s Hospital Luodong, ; Yilan, Taiwan
                [8 ]GRID grid.19188.39, ISNI 0000 0004 0546 0241, Department of Internal Medicine, National Taiwan University Hospital, College of Medicine, , National Taiwan University, ; 7 Chung-Shan South Road, Taipei, Taiwan
                [9 ]GRID grid.412094.a, ISNI 0000 0004 0572 7815, Department of Internal Medicine, , National Taiwan University Hospital, Hsin-Chu Branch, ; Hsin Chu County, Taiwan
                [10 ]Chinru Clinic, Taipei, Taiwan
                [11 ]GRID grid.239578.2, ISNI 0000 0001 0675 4725, Department of Family Medicine, , Cleveland Clinic Akron General Hospital, ; Akron, OH USA
                [12 ]GRID grid.412094.a, ISNI 0000 0004 0572 7815, National Taiwan University Hospital Study Group of ARF (NSARF), , Taiwan Consortium for Acute Kidney Injury and Renal Diseases (CAKS, TCTC), ; Taipei, Taiwan
                Author information
                http://orcid.org/0000-0001-7935-0991
                Article
                3434
                10.1186/s13054-020-03434-z
                7784335
                33402204
                13fe9281-c9fc-44e8-b42e-88424ab499e5
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

                History
                : 1 October 2020
                : 11 December 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001868, National Science Council;
                Award ID: NSC 101-2314-B-002-132-MY3
                Award ID: NSC 101-2314-B-002-085-MY3
                Award ID: MOST 104-2314-B-002 -125 -MY3
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100005762, National Taiwan University Hospital;
                Award ID: 100-N1776
                Award ID: 101-M1953
                Award ID: 102-S2097
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Emergency medicine & Trauma
                accelerated dialysis,dialysis dependence,free of dialysis,mortality,renal replacement therapy,standard dialysis

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