Evidence map›Paper›PMID 34078114›Full record

ArticleJournal of diabetes science and technology2022

Estimating Enhanced Endogenous Glucose Production in Intensive Care Unit Patients with Severe Insulin Resistance.

Anane Yahia, Ákos Szlávecz, Jennifer L Knopp, Normy Norfiza Abdul Razak, Asma Abu Samah, Geoff Shaw, J Geoffrey Chase, Balazs Benyo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of diabetes science and technology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 23% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
  4. Observational
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

8 authors at 3 institutions in 3 countries.

Anane YahiaDepartment of Control Engineering and Information Technology, Budapest University of Technology and Economics, Budapest, Hungary.ORCID 0000-0001-6751-5226
Ákos SzláveczDepartment of Control Engineering and Information Technology, Budapest University of Technology and Economics, Budapest, Hungary.
Jennifer L KnoppMechanical Engineering, Centre of Bio-Engineering, University of Canterbury, Christchurch, NZ.ORCID 0000-0001-9343-3961
Normy Norfiza Abdul RazakDepartment of Electronics and Communication Engineering, UNITEN, Malaysia.
Asma Abu SamahInstitute of Energy Infrastructure, Universiti Tenaga Nasional, Jalan Ikram-UNITEN, Kajang, Selangor, Malaysia.
Geoff ShawMechanical Engineering, Centre of Bio-Engineering, University of Canterbury, Christchurch, NZ.
J Geoffrey ChaseMechanical Engineering, Centre of Bio-Engineering, University of Canterbury, Christchurch, NZ.
Balazs BenyoDepartment of Control Engineering and Information Technology, Budapest University of Technology and Economics, Budapest, Hungary.
Budapest University of Technology and Economics · HUUniversity of Canterbury · NZUniversiti Tenaga Nasional · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCritically ill ICU patients frequently experience acute insulin resistance and increased endogenous glucose production, manifesting as stress-induced hyperglycemia and hyperinsulinemia. STAR (Stochastic TARgeted) is a glycemic control protocol, which directly manages inter- and intra- patient variability using model-based insulin sensitivity (SI). The model behind STAR assumes a population constant for endogenous glucose production (EGP), which is not otherwise identifiable.

objectiveThis study analyses the effect of estimating EGP for ICU patients with very low SI (severe insulin resistance) and its impact on identified, model-based insulin sensitivity identification, modeling accuracy, and model-based glycemic clinical control.

methodsUsing clinical data from 717 STAR patients in 3 independent cohorts (Hungary, New Zealand, and Malaysia), insulin sensitivity, time of insulin resistance, and EGP values are analyzed. A method is presented to estimate EGP in the presence of non-physiologically low SI. Performance is assessed via model accuracy.

resultsResults show 22%-62% of patients experience 1+ episodes of severe insulin resistance, representing 0.87%-9.00% of hours. Episodes primarily occur in the first 24 h, matching clinical expectations. The Malaysian cohort is most affected. In this subset of hours, constant model-based EGP values can bias identified SI and increase blood glucose (BG) fitting error. Using the EGP estimation method presented in these constrained hours significantly reduced BG fitting errors.

conclusionsPatients early in ICU stay may have significantly increased EGP. Increasing modeled EGP in model-based glycemic control can improve control accuracy in these hours. The results provide new insight into the frequency and level of significantly increased EGP in critical illness.

Indexed as

HyperglycemiaInsulin ResistanceBlood GlucoseCritical CareCritical IllnessGlucoseHumansInsulinIntensive Care UnitsBlood GlucoseGlucoseInsulinblood glucoseEGPendogenous glucose productionglycemic controlinsulin sensitivitymodel-basedSTAR

Identifiers

PMID34078114
PMCPMC9445352
OpenAlexW3164939609

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.