Evidence map›Paper›PMID 27209269›Full record

Trial reportJAMA

Effect of Early vs Delayed Initiation of Renal Replacement Therapy on Mortality in Critically Ill Patients With Acute Kidney Injury: The ELAIN Randomized Clinical Trial.

Alexander Zarbock, John A Kellum, Christoph Schmidt, Hugo Van Aken, Carola Wempe, Hermann Pavenstädt, Andreea Boanta, Joachim Gerß, Melanie Meersch

2 registry-linked trialsAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in JAMA. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 505 papers, 12 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
505citing papers in PubMed, 12 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03549923 phase4completednot on this map

Impact of Early CRRT Intervention in Patients Receiving VA-ECMO Support on 30-day Mortality: A Randomized Controlled Trial

TypeinterventionalSponsorBeijing Anzhen HospitalRan2018 to 2023Enrolled131ConditionsCardiogenic ShockArmsSimultaneous CRRT, Conventional-indication CRRT, Esmolol, Standard care
NCT06229990 phase4recruitingnot on this map

Effect of a Furosemide Stress Test-Guided Strategy on Liberation From Continuous Renal Replacement Therapy in Critically Ill Patients With Acute Kidney Injury (FST-LIBERATE)

TypeinterventionalSponsorChiang Mai UniversityRan2024 to 2028Enrolled80ConditionsAcute Kidney InjuryArmsFurosemide Injection
3 · Its place in the literature

Who cites it

505 citing papers in PubMed, 12 syntheses or guidelines pooled it.

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  4. [S3 guideline on sepsis-prevention, diagnosis, therapy, and follow-up care-update 2025].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2025
    Guideline
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  12. Timing of kidney replacement therapy initiation for acute kidney injury.The Cochrane database of systematic reviews · 2022
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445 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Alexander ZarbockDepartment of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Germany.
John A KellumCenter for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pennsylvania.
Christoph SchmidtDepartment of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Germany.
Hugo Van AkenDepartment of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Germany.
Carola WempeDepartment of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Germany.
Hermann PavenstädtDepartment of Internal Medicine D, University Hospital Münster, Germany.
Andreea BoantaDepartment of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Germany.
Joachim GerßInstitute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
Melanie MeerschDepartment of Anaesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceOptimal timing of initiation of renal replacement therapy (RRT) for severe acute kidney injury (AKI) but without life-threatening indications is still unknown.

objectiveTo determine whether early initiation of RRT in patients who are critically ill with AKI reduces 90-day all-cause mortality. DESIGN, SETTING, AND

participantsSingle-center randomized clinical trial of 231 critically ill patients with AKI Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 (≥2 times baseline or urinary output <0.5 mL/kg/h for ≥12 hours) and plasma neutrophil gelatinase-associated lipocalin level higher than 150 ng/mL enrolled between August 2013 and June 2015 from a university hospital in Germany.

interventionsEarly (within 8 hours of diagnosis of KDIGO stage 2; n = 112) or delayed (within 12 hours of stage 3 AKI or no initiation; n = 119) initiation of RRT. MAIN OUTCOMES AND MEASURES: The primary end point was mortality at 90 days after randomization. Secondary end points included 28- and 60-day mortality, clinical evidence of organ dysfunction, recovery of renal function, requirement of RRT after day 90, duration of renal support, and intensive care unit (ICU) and hospital length of stay.

resultsAmong 231 patients (mean age, 67 years; men, 146 [63.2%]), all patients in the early group (n = 112) and 108 of 119 patients (90.8%) in the delayed group received RRT. All patients completed follow-up at 90 days. Median time (Q1, Q3) from meeting full eligibility criteria to RRT initiation was significantly shorter in the early group (6.0 hours [Q1, Q3: 4.0, 7.0]) than in the delayed group (25.5 h [Q1, Q3: 18.8, 40.3]; difference, -21.0 [95% CI, -24.0 to -18.0]; P < .001). Early initiation of RRT significantly reduced 90-day mortality (44 of 112 patients [39.3%]) compared with delayed initiation of RRT (65 of 119 patients [54.7%]; hazard ratio [HR], 0.66 [95% CI, 0.45 to 0.97]; difference, -15.4% [95% CI, -28.1% to -2.6%]; P = .03). More patients in the early group recovered renal function by day 90 (60 of 112 patients [53.6%] in the early group vs 46 of 119 patients [38.7%] in the delayed group; odds ratio [OR], 0.55 [95% CI, 0.32 to 0. 93]; difference, 14.9% [95% CI, 2.2% to 27.6%]; P = .02). Duration of RRT and length of hospital stay were significantly shorter in the early group than in the delayed group (RRT: 9 days [Q1, Q3: 4, 44] in the early group vs 25 days [Q1, Q3: 7, >90] in the delayed group; P = .04; HR, 0.69 [95% CI, 0.48 to 1.00]; difference, -18 days [95% CI, -41 to 4]; hospital stay: 51 days [Q1, Q3: 31, 74] in the early group vs 82 days [Q1, Q3: 67, >90] in the delayed group; P < .001; HR, 0.34 [95% CI, 0.22 to 0.52]; difference, -37 days [95% CI, -∞ to -19.5]), but there was no significant effect on requirement of RRT after day 90, organ dysfunction, and length of ICU stay. CONCLUSIONS AND RELEVANCE: Among critically ill patients with AKI, early RRT compared with delayed initiation of RRT reduced mortality over the first 90 days. Further multicenter trials of this intervention are warranted.

trial registrationGerman Clinical Trial Registry Identifier: DRKS00004367.

Indexed as

Critical IllnessRenal Replacement TherapyAcute Kidney InjuryAcute-Phase ProteinsAgedAged, 80 and overFemaleHumansIntensive Care UnitsLength of StayLipocalin-2LipocalinsMaleMiddle AgedProto-Oncogene ProteinsSurvival AnalysisAcute-Phase ProteinsLCN2 protein, humanLipocalin-2LipocalinsProto-Oncogene Proteins

Identifiers

PMID27209269

What OpenQuestion holds

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Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.