Evidence map›Paper›PMID 22307571›Full record

Trial reportJAMA2012

Initial trophic vs full enteral feeding in patients with acute lung injury: the EDEN randomized trial.

National Heart, Lung, and Blood Institute Acute Respiratory Distress Syndrome (ARDS) Clinical Trials Network, Todd W Rice, Arthur P Wheeler, B Taylor Thompson, Jay Steingrub, R Duncan Hite, Marc Moss, Alan Morris, Ning Dong, Peter Rock

11 registry-linked trialsOpen access · greenAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 11 registered trials, which are not on this map. Cited by 356 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
356citing papers in PubMed, 13 pooled it
55.7field-weighted citation impact, top 1% of its field
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.

NCT00609180 phase3terminatednot on this map

Prospective, Randomized, Multi-Center Trial of Initial Trophic Enteral Feeding Followed by Advancement to Full-Calorie Enteral Feeding vs. Early Advancement to Full-Calorie Enteral Feeding in Patients With Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS) and Prospective, Randomized, Blinded, Placebo-Controlled, Multi-Center Trial of Omega-3 Fatty Acid, Gamma-Linolenic Acid, and Anti-Oxidant Supplementation in the Management of Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS)

TypeinterventionalSponsorNational Heart, Lung, and Blood Institute (NHLBI)Ran2007 to 2009Enrolled272ConditionsRespiratory Distress Syndrome, AdultArmsMinimal (Trophic) Feeding, Full Feeding, Omega-3 Fatty Acids and Antioxidant Supplements, Placebo
NCT00883948 phase3completednot on this map

Prospective, Randomized, Multi-Center Trial of Initial Trophic Enteral Feeding Followed by Advancement to Full-Calorie Enteral Feeding vs. Early Advancement to Full-Calorie Enteral Feeding in Patients With Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS)

TypeinterventionalSponsorNational Heart, Lung, and Blood Institute (NHLBI)Ran2007 to 2011Enrolled1,000ConditionsRespiratory Distress Syndrome, AdultArmsMinimal (Trophic) Feeding, Full Feeding
NCT02773771 phase2 / phase3withdrawnnot on this mapstarted 2017, after this paper: background citation

Strategies to Reduce Organic Muscle Atrophy in the Intensive Care Unit (STROMA-ICU)

TypeinterventionalSponsorMassachusetts General HospitalRan2017 to 2019Enrolled0ConditionsMuscle AtrophyArmsbeta-hydroxy-beta-methylbutyrate, Placebo, Vital HP®
NCT02982668 naterminatednot on this mapstarted 2017, after this paper: background citation

A Multi-center Randomised Controlled Trial to Explore the Ideal Initial Enteral Feeding Strategies in Patients With Severe Stroke at Acute Stage

TypeinterventionalSponsorXijing HospitalRan2017 to 2020Enrolled306ConditionsSevere Stroke, Acute Stroke, DysphagiaArmsInitial enteral feeding, metoclopramide or mosapride
NCT03021902 phase2completednot on this mapstarted 2017, after this paper: background citation

Nutrition and Exercise in Critical Illness (The NEXIS Trial): A Randomized Trial of Combined Cycle Ergometry and Amino Acids in the ICU

TypeinterventionalSponsorClinical Evaluation Research Unit at Kingston General HospitalRan2017 to 2025Enrolled115ConditionsAcute Respiratory FailureArmsIV amino acids, In-bed cycle ergometry exercise
NCT03115957 nacompletednot on this mapstarted 2017, after this paper: background citation

Early Versus Delayed Parenteral Nutrition in Abdominal Surgical Patients With Nutritional Risk and Initial Enteral Nutrition Intolerance: A Clinical Randomized Trial

TypeinterventionalSponsorJinling Hospital, ChinaRan2017 to 2019Enrolled230ConditionsDigestive System NeoplasmsArmsParenteral Nutrition
NCT03117348 nacompletednot on this mapstarted 2017, after this paper: background citation

Gradual Versus Immediate Goal-dose Enteral Nutrition in Abdominal Surgery Patients: A Clinical Randomized Controlled Trial

TypeinterventionalSponsorJinling Hospital, ChinaRan2017 to 2019Enrolled411ConditionsEnteral Nutrition, Postoperative Period, Digestive System NeoplasmsArmsEnteral nutrition
NCT03469882 nacompletednot on this mapstarted 2018, after this paper: background citation

High Protein Intake and Early Exercise in Adult Intensive Care Patients: Impact on Functional Outcomes. A Randomized Controlled Phase II Trial.

TypeinterventionalSponsorHospital Sao DomingosRan2018 to 2020Enrolled180ConditionsCritically Ill PatientsArmsHigh protein nutrition, Cycle ergometry exercise, Usual care group
NCT03634943 completednot on this mapstarted 2018, after this paper: background citation

Evaluation of Nutritional Practices in the Critical Care Patient at the Intensive Care Unit

TypeobservationalSponsorHospital Universitari de BellvitgeRan2018 to 2022Enrolled642ConditionsNutritional Support, Intensive Care Unit, Critical IllnessArmsPatients with Nutritional Support
NCT04242966 phase3withdrawnnot on this mapstarted 2020, after this paper: background citation

The Effect of Higher Protein Dosing in Critically Ill Patients: A Multicenter Registry-based Randomized Trial: The EFFORT Ultrasound a Sub-study

TypeinterventionalSponsorClinical Evaluation Research Unit at Kingston General HospitalRan2020 to 2022Enrolled0ConditionsCritical Illness, MalnutritionArmsUsual Care, Higher Protein/Amino Acid Group, Ultrasound measure
NCT05998902 phase3completednot on this mapstarted 2023, after this paper: background citation

Trophic Enteral Feeding Combined With Supplemental Parenteral Nutrition Treatment in Patients With Severe Stroke (OPENS-2): a Multicentre, Prospective, Randomised, Open-label, Blinded-endpoint Trial

TypeinterventionalSponsorWen Jiang-3Ran2023 to 2026Enrolled546ConditionsSevere Stroke, Acute Stroke, DysphagiaArmsTrophic enteral feeding combined with supplemental parenteral nutrition, Full enteral feeding
3 · Its place in the literature

Who cites it

356 citing papers in PubMed, 13 syntheses or guidelines pooled it, 920 citations in OpenAlex.

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  11. Between-trial heterogeneity in ARDS research.Intensive care medicine · 2021
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  12. [S3 Guideline Sepsis-prevention, diagnosis, therapy, and aftercare : Long version].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2020
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296 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

National Heart, Lung, and Blood Institute Acute Respiratory Distress Syndrome (ARDS) Clinical Trials Network
Todd W Rice
Arthur P Wheeler
B Taylor Thompson
Jay Steingrub
R Duncan Hite
Marc Moss
Alan Morris
Ning Dong
Peter Rock

Funding

Lung Surfactant Activity, Inhibition and ReplacementR01HL056176 · NHLBI · UNIVERSITY OF ROCHESTER · PI NOTTER, ROBERT H · 1997 to 2006
$1.8M
Ferritin and Iron Nutrition in Health and DiseaseR01HL056169 · NHLBI · CHILDREN'S HOSPITAL &RES CTR AT OAKLAND · PI THEIL, ELIZABETH C · 1998 to 2005
$1.6M
Clin Coord Ctr for Clin Ntwrk Treatment of ARDS-268056179-268056179N01HR056179 · HR · MASSACHUSETTS GENERAL HOSPITAL · PI SCHOENFELD, DAVID · 2005 to 2006
–
NHLBI NIH HHS N01 HR056165NHLBI NIH HHS N01 HR056166NHLBI NIH HHS N01 HR056167NHLBI NIH HHS N01 HR056168NHLBI NIH HHS N01 HR056169NHLBI NIH HHS N01 HR056170NHLBI NIH HHS N01 HR056171NHLBI NIH HHS N01 HR056172NHLBI NIH HHS N01 HR056173NHLBI NIH HHS N01 HR056174NHLBI NIH HHS N01 HR056175NHLBI NIH HHS N01 HR056176NHLBI NIH HHS N01 HR056179PHS HHS HHSN268200536165CPHS HHS HHSN268200536179C
6 · The paper itself

Abstract

contextThe amount of enteral nutrition patients with acute lung injury need is unknown.

objectiveTo determine if initial lower-volume trophic enteral feeding would increase ventilator-free days and decrease gastrointestinal intolerances compared with initial full enteral feeding. DESIGN, SETTING, AND

participantsThe EDEN study, a randomized, open-label, multicenter trial conducted from January 2, 2008, through April 12, 2011. Participants were 1000 adults within 48 hours of developing acute lung injury requiring mechanical ventilation whose physicians intended to start enteral nutrition at 44 hospitals in the National Heart, Lung, and Blood Institute ARDS Clinical Trials Network.

interventionsParticipants were randomized to receive either trophic or full enteral feeding for the first 6 days. After day 6, the care of all patients who were still receiving mechanical ventilation was managed according to the full feeding protocol.

main outcome measuresVentilator-free days to study day 28.

resultsBaseline characteristics were similar between the trophic-feeding (n = 508) and full-feeding (n = 492) groups. The full-feeding group received more enteral calories for the first 6 days, about 1300 kcal/d compared with 400 kcal/d (P < .001). Initial trophic feeding did not increase the number of ventilator-free days (14.9 [95% CI, 13.9 to 15.8] vs 15.0 [95% CI, 14.1 to 15.9]; difference, -0.1 [95% CI, -1.4 to 1.2]; P = .89) or reduce 60-day mortality (23.2% [95% CI, 19.6% to 26.9%] vs 22.2% [95% CI, 18.5% to 25.8%]; difference, 1.0% [95% CI, -4.1% to 6.3%]; P = .77) compared with full feeding. There were no differences in infectious complications between the groups. Despite receiving more prokinetic agents, the full-feeding group experienced more vomiting (2.2% vs 1.7% of patient feeding days; P = .05), elevated gastric residual volumes (4.9% vs 2.2% of feeding days; P < .001), and constipation (3.1% vs 2.1% of feeding days; P = .003). Mean plasma glucose values and average hourly insulin administration were both higher in the full-feeding group over the first 6 days.

conclusionIn patients with acute lung injury, compared with full enteral feeding, a strategy of initial trophic enteral feeding for up to 6 days did not improve ventilator-free days, 60-day mortality, or infectious complications but was associated with less gastrointestinal intolerance.

trial registrationclinicaltrials.gov Identifiers: NCT00609180 and NCT00883948.

Indexed as

Acute Lung InjuryEnergy IntakeRespiration, ArtificialAdultAgedEnteral NutritionFemaleGastrointestinal TractHumansInfectionsMaleMiddle AgedProspective StudiesTime FactorsTreatment Outcome

Identifiers

PMID22307571
PMCPMC3743415
OpenAlexW2160722967

What OpenQuestion holds

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Registered trials

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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.