Evidence map›Paper›PMID 25272316›Full record

Trial reportThe New England journal of medicine2014

Goal-directed resuscitation for patients with early septic shock.

ARISE Investigators, ANZICS Clinical Trials Group, Sandra L Peake, Anthony Delaney, Michael Bailey, Rinaldo Bellomo, Peter A Cameron, D James Cooper, Alisa M Higgins, Anna Holdgate and 3 more

12 registry-linked trialsAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in The New England journal of medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 12 registered trials, which are not on this map. Cited by 768 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
768citing papers in PubMed, 7 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.

NCT00975793 phase3unknown statusnot on this map

A Multi-centre, Randomised Controlled Trial of Early Goal-directed Therapy in Patients Presenting to the Emergency Department With Severe Sepsis in Australasia

TypeinterventionalSponsorBelinda HoweRan2008 to 2015Enrolled1,600ConditionsSevere SepsisArmsEarly Goal Directed Therapy (EGDT)
NCT02565251 naunknown statusnot on this mapstarted 2015, after this paper: background citation

Volemic Resuscitation in Sepsis and Septic Shock

TypeinterventionalSponsorIuliu Hatieganu University of Medicine and PharmacyRan2015 to 2017Enrolled100ConditionsHemodynamic Instability, Sepsis, Septic ShockArmsFlotrac/Ev1000, Standard ICU monitorisation, VolumeView/Ev1000
NCT02950753 early_phase1completednot on this mapstarted 2017, after this paper: background citation

Does Intravenous Lactated Ringer Solution Raise Measured Serum Lactate?

TypeinterventionalSponsorUniversity Medical Center of Southern NevadaRan2017 to 2017Enrolled30ConditionsHyperlactatemiaArmsLactated Ringer Solution, Normal Saline
NCT03137446 nacompletednot on this mapstarted 2017, after this paper: background citation

Assessing Targeted Fluid Resuscitation Strategies Among Patients With Severe Sepsis and Septic Shock

TypeinterventionalSponsorRhode Island HospitalRan2017 to 2018Enrolled113ConditionsSeptic Shock, Severe SepsisArmsIntravenous Fluid Cap
NCT03214913 naunknown statusnot on this mapstarted 2018, after this paper: background citation

Controlled Fluid Resuscitation Strategy in Sepsis Patient

TypeinterventionalSponsorRuijin HospitalRan2018 to 2021Enrolled550ConditionsSepsisArmsEarly Goal Directed Therapy, Ruijin Strategy
NCT03422159 phase2completednot on this mapstarted 2018, after this paper: background citation

Outcomes of Metabolic Resuscitation Using Ascorbic Acid, Thiamine, and Glucocorticoids in the Early Treatment of Sepsis.

TypeinterventionalSponsorCommunity Medical Center, Toms River, NJRan2018 to 2019Enrolled140ConditionsSepsis, Severe, Septic ShockArmsAscorbic Acid, Thiamine, Hydrocortisone, Sodium Chloride 0.9%
NCT04567433 completednot on this mapstarted 2020, after this paper: background citation

Days Alive and Out of Hospital for Patients With Sepsis

TypeobservationalSponsorThe George Institute for Global Health, AustraliaRan2020 to 2024Enrolled6,213ConditionsSepsis, Septic ShockArmsHydroxyethyl starch, Hydrocortisone, Early Goal Directed Therapy
NCT04742764 phase3suspendednot on this mapstarted 2024, after this paper: background citation

Dosing of Extracorporeal Cytokine Removal In Septic Shock (DECRISS): a Prospective, Randomized, Multicenter Clinical Trial

TypeinterventionalSponsorUniversity of PecsRan2024 to 2027Enrolled135ConditionsSeptic ShockArmsStandard medical therapy, Standard medical therapy plus cytokine removal treatment using Cytosorb, with the adsorber changed in every 12 hours, Standard medical therapy plus cytokine removal treatment using Cytosorb, with the adsorber changed in every 24 hours
NCT05059795 completednot on this mapstarted 2020, after this paper: background citation

To Compare the Effectiveness of Various Methods of Estimating Volume Resuscitation in Patients With Cirrhosis With Sepsis Induced Hypotension

TypeobservationalSponsorPost Graduate Institute of Medical Education and Research, ChandigarhRan2020 to 2025Enrolled350ConditionsCirrhosis, Liver, Sepsis, Acute on Chronic Liver FailureArmsAlbumin + electrolyte solution, POCUS guided fluid resuscitation
NCT05441878 phase4unknown statusnot on this mapstarted 2020, after this paper: background citation

To Compare 20% Albumin vs. Balanced Salt Solution as Resuscitation Fluid and Identify Fluid Responsiveness Criteria in Critically Ill Patients With Cirrhosis With Sepsis Induced Hypotension; a Prospective Randomized Controlled Trial.

TypeinterventionalSponsorPost Graduate Institute of Medical Education and Research, ChandigarhRan2020 to 2023Enrolled150ConditionsCirrhosis, Liver, Acute-On-Chronic Liver Failure, Shock, Septic, Shock HypovolemicArms20% albumin, Balanced salt solution
NCT07172451 phase4recruitingnot on this mapstarted 2026, after this paper: background citation

Efficacy and Safety of Balanced Gelatin Solution for Fluid Infusion in Sepsis Patients Undergoing Emergency Abdominal Surgery: A Multicenter, Adaptive Designed, Randomized Controlled Trial

TypeinterventionalSponsorShanghai Zhongshan HospitalRan2026 to 2028Enrolled318ConditionsSepsis, Intra-Abdominal InfectionsArmsBalanced Gelatin Solution, Acetate Ringer's Solution
NCT07179276 narecruitingnot on this mapstarted 2026, after this paper: background citation

Veno-arterial Carbon Dioxide Partial Pressure Difference (CO2gap) for Early Resuscitation of Septic Shock: A Multicenter Prospective Randomized Trial (CARBON)

TypeinterventionalSponsorUniversity Hospital, Clermont-FerrandRan2026 to 2027Enrolled750ConditionsSepsis - to Reduce Mortality in the Intensive Care Unit, Septic ShockArmsCO2gap-guided resuscitation strategy
3 · Its place in the literature

Who cites it

768 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Pooled it
  2. [S3 guideline on sepsis-prevention, diagnosis, therapy, and follow-up care-update 2025].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2025
    Guideline
  3. Pooled it
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708 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

ARISE Investigators
ANZICS Clinical Trials Group
Sandra L Peake
Anthony Delaney
Michael Bailey
Rinaldo Bellomo
Peter A Cameron
D James Cooper
Alisa M Higgins
Anna Holdgate
Belinda D Howe
Steven A R Webb
Patricia Williams

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly goal-directed therapy (EGDT) has been endorsed in the guidelines of the Surviving Sepsis Campaign as a key strategy to decrease mortality among patients presenting to the emergency department with septic shock. However, its effectiveness is uncertain.

methodsIn this trial conducted at 51 centers (mostly in Australia or New Zealand), we randomly assigned patients presenting to the emergency department with early septic shock to receive either EGDT or usual care. The primary outcome was all-cause mortality within 90 days after randomization.

resultsOf the 1600 enrolled patients, 796 were assigned to the EGDT group and 804 to the usual-care group. Primary outcome data were available for more than 99% of the patients. Patients in the EGDT group received a larger mean (±SD) volume of intravenous fluids in the first 6 hours after randomization than did those in the usual-care group (1964±1415 ml vs. 1713±1401 ml) and were more likely to receive vasopressor infusions (66.6% vs. 57.8%), red-cell transfusions (13.6% vs. 7.0%), and dobutamine (15.4% vs. 2.6%) (P<0.001 for all comparisons). At 90 days after randomization, 147 deaths had occurred in the EGDT group and 150 had occurred in the usual-care group, for rates of death of 18.6% and 18.8%, respectively (absolute risk difference with EGDT vs. usual care, -0.3 percentage points; 95% confidence interval, -4.1 to 3.6; P=0.90). There was no significant difference in survival time, in-hospital mortality, duration of organ support, or length of hospital stay.

conclusionsIn critically ill patients presenting to the emergency department with early septic shock, EGDT did not reduce all-cause mortality at 90 days. (Funded by the National Health and Medical Research Council of Australia and the Alfred Foundation; ARISE ClinicalTrials.gov number, NCT00975793.).

Indexed as

Fluid TherapyAdultAgedCombined Modality TherapyCritical IllnessDobutamineEmergency Service, HospitalErythrocyte TransfusionFemaleHumansLength of StayMaleMiddle AgedRenal Replacement TherapyRespiration, ArtificialShock, SepticDobutamineVasoconstrictor Agents

Identifiers

PMID25272316

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 6 more above

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.