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      Regional Practice Variation and Outcomes in the Standard Versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Trial: A Post Hoc Secondary Analysis

      research-article
      , MD, PhD 1 , , , MD, PhD 2 , 3 , 4 , 5 , , MD, PhD 2 , 3 , 4 , 6 , 7 , , MDCM, MSc 8 , 9 , 10 , , MD, PhD 11 , 12 , , MD, PhD 13 , 14 , , MD, PhD 11 , 15 , , MD, PhD 16 , , MD 17 , , MD, PhD 1 , , MD, PhD 13 , 14 , 18 , , MD, PhD 19 , , MDCM, MPH 20 , 21 , , MD, MSc 22 , , MD, PhD 23 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
      Critical Care Explorations
      Lippincott Williams & Wilkins
      acute kidney injury, continuous renal replacement therapy, fluid balance, intermittent hemodialysis, outcomes, randomized controlled trial

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          Abstract

          OBJECTIVES:

          Among patients with severe acute kidney injury (AKI) admitted to the ICU in high-income countries, regional practice variations for fluid balance (FB) management, timing, and choice of renal replacement therapy (RRT) modality may be significant.

          DESIGN:

          Secondary post hoc analysis of the STandard vs. Accelerated initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial (ClinicalTrials.gov number NCT02568722).

          SETTING:

          One hundred-fifty-three ICUs in 13 countries.

          PATIENTS:

          Altogether 2693 critically ill patients with AKI, of whom 994 were North American, 1143 European, and 556 from Australia and New Zealand (ANZ).

          INTERVENTIONS:

          None.

          MEASUREMENTS AND MAIN RESULTS:

          Total mean FB to a maximum of 14 days was +7199 mL in North America, +5641 mL in Europe, and +2211 mL in ANZ ( p < 0.001). The median time to RRT initiation among patients allocated to the standard strategy was longest in Europe compared with North America and ANZ ( p < 0.001; p < 0.001). Continuous RRT was the initial RRT modality in 60.8% of patients in North America and 56.8% of patients in Europe, compared with 96.4% of patients in ANZ ( p < 0.001). After adjustment for predefined baseline characteristics, compared with North American and European patients, those in ANZ were more likely to survive to ICU ( p < 0.001) and hospital discharge ( p < 0.001) and to 90 days (for ANZ vs. Europe: risk difference [RD], –11.3%; 95% CI, –17.7% to –4.8%; p < 0.001 and for ANZ vs. North America: RD, –10.3%; 95% CI, –17.5% to –3.1%; p = 0.007).

          CONCLUSIONS:

          Among STARRT-AKI trial centers, significant regional practice variation exists regarding FB, timing of initiation of RRT, and initial use of continuous RRT. After adjustment, such practice variation was associated with lower ICU and hospital stay and 90-day mortality among ANZ patients compared with other regions.

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          Most cited references39

          • Record: found
          • Abstract: found
          • Article: not found

          Epidemiology of acute kidney injury in critically ill patients: the multinational AKI-EPI study.

          Current reports on acute kidney injury (AKI) in the intensive care unit (ICU) show wide variation in occurrence rate and are limited by study biases such as use of incomplete AKI definition, selected cohorts, or retrospective design. Our aim was to prospectively investigate the occurrence and outcomes of AKI in ICU patients.
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            Acute renal failure in critically ill patients: a multinational, multicenter study.

            Although acute renal failure (ARF) is believed to be common in the setting of critical illness and is associated with a high risk of death, little is known about its epidemiology and outcome or how these vary in different regions of the world. To determine the period prevalence of ARF in intensive care unit (ICU) patients in multiple countries; to characterize differences in etiology, illness severity, and clinical practice; and to determine the impact of these differences on patient outcomes. Prospective observational study of ICU patients who either were treated with renal replacement therapy (RRT) or fulfilled at least 1 of the predefined criteria for ARF from September 2000 to December 2001 at 54 hospitals in 23 countries. Occurrence of ARF, factors contributing to etiology, illness severity, treatment, need for renal support after hospital discharge, and hospital mortality. Of 29 269 critically ill patients admitted during the study period, 1738 (5.7%; 95% confidence interval [CI], 5.5%-6.0%) had ARF during their ICU stay, including 1260 who were treated with RRT. The most common contributing factor to ARF was septic shock (47.5%; 95% CI, 45.2%-49.5%). Approximately 30% of patients had preadmission renal dysfunction. Overall hospital mortality was 60.3% (95% CI, 58.0%-62.6%). Dialysis dependence at hospital discharge was 13.8% (95% CI, 11.2%-16.3%) for survivors. Independent risk factors for hospital mortality included use of vasopressors (odds ratio [OR], 1.95; 95% CI, 1.50-2.55; P<.001), mechanical ventilation (OR, 2.11; 95% CI, 1.58-2.82; P<.001), septic shock (OR, 1.36; 95% CI, 1.03-1.79; P = .03), cardiogenic shock (OR, 1.41; 95% CI, 1.05-1.90; P = .02), and hepatorenal syndrome (OR, 1.87; 95% CI, 1.07-3.28; P = .03). In this multinational study, the period prevalence of ARF requiring RRT in the ICU was between 5% and 6% and was associated with a high hospital mortality rate.
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              Global epidemiology and outcomes of acute kidney injury

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                Author and article information

                Journal
                Crit Care Explor
                Crit Care Explor
                CC9
                Critical Care Explorations
                Lippincott Williams & Wilkins (Hagerstown, MD )
                2639-8028
                19 February 2024
                February 2024
                : 6
                : 2
                : e1053
                Affiliations
                [1 ] Department of Perioperative and Intensive Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
                [2 ] Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
                [3 ] Department of Critical Care, Melbourne Medical School, University of Melbourne, Austin Hospital, Melbourne, VIC, Australia.
                [4 ] Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia.
                [5 ] Department of Critical Care Medicine, Hospital Israelita Albert Einstein, Sao Paulo, Brazil.
                [6 ] Data Analytics Research & Evaluation, Austin Hospital, Melbourne, VIC, Australia.
                [7 ] Department of Intensive Care, Royal Melbourne Hospital, Melbourne, VIC, Australia.
                [8 ] Department of Critical Care Medicine, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
                [9 ] Institute of Health Policy, Management and Evaluation, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
                [10 ] Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, ON, Canada.
                [11 ] French National Institute of Health and Medical Research (INSERM), UMR_S1155, CORAKID, Hôpital Tenon, Sorbonne Université, Paris, France.
                [12 ] Service de Médecine Intensive Réanimation, Hôpital Louis Mourier, Assistance Publique, Université de Paris-Cité, Paris, France.
                [13 ] South Western Sydney Clinical Campus, Faculty of Medicine & Health, University of New South Wales, New South Wales, NSW, Australia.
                [14 ] The George Institute for Global Health, University of New South Wales, New South Wales, Australia.
                [15 ] AP-HP, Hôpital Avicenne, Service de Réanimation Médico-Chirurgicale, UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France.
                [16 ] Intensive Care Unit, Department of Internal Medicine and Pediatrics, Ghent University Hospital, Ghent University, Ghent, Belgium.
                [17 ] Division of Intensive Care and Emergency Medicine, Department of Internal Medicine, Medical University Innsbruck, Innsbruck, Austria.
                [18 ] The Faculty of Medicine and Medical Sciences, Macquarie University, Sydney, NSW, Australia.
                [19 ] Division of Nephrology and Hypertension, Division of Pulmonary and Critical Care Medicine, Department of Medicine, Mayo Clinic College of Medicine, Rochester, MN.
                [20 ] Medicine Program and Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Unity Health Toronto, Toronto, ON, Canada.
                [21 ] Division of Nephrology, St. Michael’s Hospital and the University of Toronto and the Li Ka Shing Knowledge Institute of St. Michael’s Hospital, Toronto, ON, Canada.
                [22 ] Department of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta and Alberta Health Services, Edmonton, AB, Canada.
                [23 ] Department of Critical Care Medicine, King’s College London, Guy’s & St Thomas’ Hospital, London, United Kingdom.
                Author notes
                For information regarding this article, E-mail: suvi.vaara@ 123456helsinki.fi
                Article
                00016
                10.1097/CCE.0000000000001053
                10878545
                38380940
                12807cae-7b00-448a-b769-3d4f3f7c3cdf
                Copyright © 2024 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine.

                This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Funding
                Funded by: Canadian Institutes of Health Research, doi 10.13039/501100000024;
                Award ID: MOP142296 and Project Grant 389635
                Award Recipient : Sean Bagshaw
                Funded by: National Health Medical Research Council of Australia
                Award ID: Project Grant 1127121)
                Award Recipient : Martin Gallgher
                Funded by: National Institutes of Health Research Health Technology Assessment Program (United Kingdom
                Award ID: Reference Number: 17/42/74)
                Award Recipient : Marlies Ostermann
                Categories
                Original Clinical Report
                Custom metadata
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                T

                acute kidney injury,continuous renal replacement therapy,fluid balance,intermittent hemodialysis,outcomes,randomized controlled trial

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