Evidence map›Paper›PMID 21789167›Full record

Trial reportPloS one2011

Long-term persistance of the pathophysiologic response to severe burn injury.

Marc G Jeschke, Gerd G Gauglitz, Gabriela A Kulp, Celeste C Finnerty, Felicia N Williams, Robert Kraft, Oscar E Suman, Ronald P Mlcak, David N Herndon

2 registry-linked trialsOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2011. 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 334 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
334citing papers in PubMed, 8 pooled it
16.8field-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.

NCT03024931 unknown statusnot on this mapstarted 2017, after this paper: background citation

In Vivo Cellular and Physiological Response to Severe Burns Injuries

TypeobservationalSponsorChelsea and Westminster NHS Foundation TrustRan2017 to 2019Enrolled10ConditionsBurnsArmsobservational study
NCT07329595 recruitingnot on this mapstarted 2023, after this paper: background citation

Monitoring the Clinical and Immunological Effects of Microbiome Changes Following Severe Burn Injury

TypeobservationalSponsorTamas Vegh, MDRan2023 to 2026Enrolled30ConditionsSeverely Burned Patients, Gut Microbiota Diversity and Composition, Inflammatory Responses
3 · Its place in the literature

Who cites it

334 citing papers in PubMed, 8 syntheses or guidelines pooled it, 604 citations in OpenAlex.

  1. Pooled it
  2. Determination of Burn Size in Mouse Models of Burn Injury: A Scoping Review of Studies Leveraging Scald and Contact Burns.Journal of burn care & research : official publication of the American Burn Association · 2025
    Pooled it
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  8. Guideline
  9. Trial
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  13. Gastric emptying after athletic carbohydrate supplementation: implications for orthopaedic trauma patients.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2026
    Article
  14. Review
  15. Pharmaceuticals (Basel, Switzerland) · 2026
    Article
  16. Review
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274 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 3 countries.

Marc G JeschkeShriners Hospitals for Children, University of Texas Medical Branch, Galveston, Texas, United States of America. marc.jeschke@sunnybrook.ca
Gerd G Gauglitz
Gabriela A Kulp
Celeste C Finnerty
Felicia N Williams
Robert Kraft
Oscar E Suman
Ronald P Mlcak
David N Herndon
Shriners Hospitals for Children - Galveston · USSunnybrook Health Science Centre · CA

Funding

MODULATION OF THE POSTBURN HYPERMETABOLIC RESPONSER01GM056687 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HERNDON, DAVID N. · 1998 to 2017
$9.0M
Oxandrolone and Exercise: A potent therapy in the rehabilitation from burnsR01HD049471 · NICHD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SUMAN-VEJAS, OSCAR E. · 2006 to 2019
$5.8M
POSTDOCTORAL TRAINING IN TRAUMA &BURNST32GM008256 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI Celeste Campbell Finnerty, Oscar E. Suman-Vejas · 1990 to 2026
$4.0M
NICHD NIH HHS R01 HD049471NIGMS NIH HHS P50 GM603380NIGMS NIH HHS R01 GM056687NIGMS NIH HHS R01-GM56687NIGMS NIH HHS T32 GM008256
6 · The paper itself

Abstract

backgroundMain contributors to adverse outcomes in severely burned pediatric patients are profound and complex metabolic changes in response to the initial injury. It is currently unknown how long these conditions persist beyond the acute phase post-injury. The aim of the present study was to examine the persistence of abnormalities of various clinical parameters commonly utilized to assess the degree hypermetabolic and inflammatory alterations in severely burned children for up to three years post-burn to identify patient specific therapeutic needs and interventions. METHODOLOGY/PRINCIPAL

findingsPATIENTS: Nine-hundred seventy-seven severely burned pediatric patients with burns over 30% of the total body surface admitted to our institution between 1998 and 2008 were enrolled in this study and compared to a cohort non-burned, non-injured children. Demographics and clinical outcomes, hypermetabolism, body composition, organ function, inflammatory and acute phase responses were determined at admission and subsequent regular intervals for up to 36 months post-burn. Statistical analysis was performed using One-way ANOVA, Student's t-test with Bonferroni correction where appropriate with significance accepted at p<0.05. Resting energy expenditure, body composition, metabolic markers, cardiac and organ function clearly demonstrated that burn caused profound alterations for up to three years post-burn demonstrating marked and prolonged hypermetabolism, p<0.05. Along with increased hypermetabolism, significant elevation of cortisol, catecholamines, cytokines, and acute phase proteins indicate that burn patients are in a hyperinflammatory state for up to three years post-burn p<0.05.

conclusionsSevere burn injury leads to a much more profound and prolonged hypermetabolic and hyperinflammatory response than previously shown. Given the tremendous adverse events associated with the hypermetabolic and hyperinflamamtory responses, we now identified treatment needs for severely burned patients for a much more prolonged time.

Indexed as

Acute-Phase ReactionBlood ProteinsBurnsChildDemographyEpinephrineFemaleHumansInflammationLiverMaleNorepinephrineTime FactorsBlood ProteinsEpinephrineNorepinephrine

Identifiers

PMID21789167
PMCPMC3138751
OpenAlexW1983984331

What OpenQuestion holds

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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.