Evidence map›Paper›PMID 41789037›Full record

ArticleJournal of the West African College of Surgeons

Glycaemic Variability and Its Outcome in Intensive Care Unit Patients with Sepsis.

Spoorthi P Yadagudde, Jayannan Jayasenan, Krishnaswamy Srinivasagalu

Abstract read
In one paragraph

Article in Journal of the West African College of Surgeons. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

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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

3 citing papers in PubMed.

  1. Article
  2. Observational
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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

3 authors.

Spoorthi P YadaguddeDepartment of General Medicine, Meenakshi Medical College Hospital and Research Institute, Meenakshi Academy of Higher Education and Research (Deemed to be University), Kanchipuram, Tamil Nadu, India.
Jayannan JayasenanDepartment of General Medicine, Meenakshi Medical College Hospital and Research Institute, Meenakshi Academy of Higher Education and Research (Deemed to be University), Kanchipuram, Tamil Nadu, India.
Krishnaswamy SrinivasagaluDepartment of General Medicine, Meenakshi Medical College Hospital and Research Institute, Meenakshi Academy of Higher Education and Research (Deemed to be University), Kanchipuram, Tamil Nadu, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sepsis causes an uncontrollable activation of pro- and anti-inflammatory responses, leading to metabolic derangements, notably glucose variability (GV). Both hyperglycaemia and hypoglycaemia can occur in septic patients, regardless of the diabetes status. Hyperglycaemia control using insulin has been shown to reduce morbidity and mortality. Current guidelines suggest maintaining glucose levels between 140 and 180 mg/dL for better clinical outcomes. Managing glycaemic variability is crucial in reducing mortality in intensive care unit (ICU) patients with sepsis. Materials and Methods: The study included patients aged ≥ 18 years, admitted for ≥ 24 h, focussing on the first 5 days of ICU stay. Data on patient characteristics, glucose values, comorbidities, organ failures, and outcomes were collected. GV was assessed, and comorbidities were determined using diagnostic codes. Results: Among a group of 100 patients (mean age 54.16 ± 18.5 years; 66% male), diabetes mellitus (84%) and hypertension (57%) were the most common comorbidities. Pneumonia (25%) and urosepsis (22%) were the primary sources of sepsis. Patients with multiple organ dysfunction syndrome (MODS) had significantly higher mean glucose levels (MGLs) than those without ( Conclusion: Higher glycaemic variability and MGLs were associated with increased mortality and MODS in ICU patients with sepsis. Improved outcomes were observed in patients with lower glycaemic variability, highlighting the need for insulin protocols to maintain optimal glucose control and reduce variability in critical care settings.

Indexed as

Coefficient of variationglycaemic variabilitymean blood glucoseMODSmortality

Identifiers

PMID41789037
PMCPMC12959862

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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.