Evidence map›Paper›PMID 19359917›Full record

ArticleThe Journal of trauma2009

Characterization of persistent hyperglycemia: what does it mean postinjury?

Jason L Sperry, Heidi L Frankel, Avery B Nathens, Grant E O'keefe, Joseph Cuschieri, Ernest E Moore, Ronald V Maier, Joseph P Minei, Inflammation and the Host Response to Injury Investigators

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of trauma, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00257231 (Inflammation and the Host Response to Injury), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 16% 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.

NCT00257231 completednot on this map

Inflammation and the Host Response to Injury

TypeobservationalSponsorMassachusetts General HospitalRan2003 to 2018Enrolled610ConditionsTrauma, Burns, Multiple Organ Failure
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Relationship of hyperglycemia and surgical-site infection in orthopaedic surgery.The Journal of bone and joint surgery. American volume · 2012
    Article
  6. Article
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  8. Review
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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 5 institutions in 2 countries.

Jason L SperryDivision of Trauma and General Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, USA. sperryjl@upmc.edu
Heidi L Frankel
Avery B Nathens
Grant E O'keefe
Joseph Cuschieri
Ernest E Moore
Ronald V Maier
Joseph P Minei
Inflammation and the Host Response to Injury Investigators
University of Washington · USThe University of Texas Southwestern Medical Center · USUniversity of Colorado Denver · USUniversity of Pittsburgh · USUniversity of Toronto · CA

Funding

Inflammation and the Response to InjuryU54GM062119 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI TOMPKINS, RONALD GARY · 2001 to 2010
$78.6M
NIGMS NIH HHS U54 GM062119NIGMS NIH HHS U54 GM062119-1
6 · The paper itself

Abstract

backgroundStrict glycemic control has been shown to reduce both morbidity and mortality in critically ill surgical patients; however, overly aggressive management of hyperglycemia may also be associated with deleterious effects. We sought to characterize clinical outcomes associated with different levels of persistent hyperglycemia (PH) in a cohort of severely injured patients with trauma, when a strict glycemic control protocol (target glucose 80-110 mg/dL) was implemented.

methodsData were obtained from a multicenter prospective cohort study evaluating clinical outcomes in blunt injured adults with hemorrhagic shock. Glycemic control was analyzed using the average maximum daily glucose values from postinjury day 2 (>48 hours after injury) to postinjury day 5. PH was defined as a mean glucose value >130 mg/dL, and was categorized into three different severity levels (I-III) based on the distribution of mean 4-day glucose values for the cohort. Separate Cox proportional hazard regression models were then used to determine whether PH was independently associated with mortality and nosocomial infection (NI), and the level of glycemic control that was associated with these poor outcomes.

resultsOverall mortality and NI rates for the study population (n = 862) were 10.8% and 49.6%, respectively. Cox proportional hazard regression revealed that PH was independently associated with almost an 80% higher mortality in patients with mean 4-day glucose values >145 mg/dL (group II) and almost a twofold higher mortality in patients with >165 mg/dL (group III). However, PH was not independently associated with a higher risk of NI at any level. Patients with PH did have a higher incidence of early multiple organ failure (within first 48 hours: 30.2% vs. 41.6% p = 0.001), which preceded the documentation of PH in the majority of patients.

conclusionMaintenance of daily maximum glucose values <145 mg/dL was independently associated with a survival benefit after injury. Patients with PH, despite aggressive insulin therapy, had a higher incidence of multiple organ failure and an associated higher risk of mortality. However, the strict glycemic control protocol in the current trauma cohort seems to have prevented the association of PH and infectious complications, which has been documented in prior studies. This analysis further validates the importance of strict glycemic control after injury, and highlights the need for further studies on the mechanism responsible for these findings.

Indexed as

AdultBlood GlucoseComorbidityCritical IllnessCross InfectionFemaleHumansHyperglycemiaMaleMiddle AgedMultiple Organ FailureProportional Hazards ModelsShock, HemorrhagicWounds, NonpenetratingBlood Glucose

Identifiers

PMID19359917
PMCPMC4004069
OpenAlexW2053890147

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.