Evidence map›Paper›PMID 41998704›Full record

Observational studyCritical care (London, England)2026

Early detection of glycocalyx and microvascular damage in suspected sepsis in the emergency department: the EDGE study.

Melina Mascha Scarbeck, Marc-David Künnemann, Anna M Hunkemöller, Carolin Christina Drost, Alexander Lukasz, Marcel Birkner, Manfred Fobker, Jerzy-Roch Nofer, Hans Vink, Hermann Pavenstädt and 2 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Critical care (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03126032 (Early Detection of Glycocalyx Damage in Emergency Room Patients), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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.

NCT03126032 completednot on this map

Early Detection of Glycocalyx Damage in Emergency Room Patients

TypeobservationalSponsorUniversity Hospital MuensterRan2017 to 2019Enrolled260ConditionsSepsis, SIRSArmsGlycoCheck™-System
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

12 authors.

Melina Mascha Scarbeck *Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Marc-David Künnemann *Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Anna M HunkemöllerDepartment of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Carolin Christina DrostDepartment of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Alexander LukaszDepartment of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Marcel BirknerDepartment of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Manfred FobkerCentral Laboratory Facility, University Hospital Münster, Albert-Schweitzer- Campus 1, 48149, Münster, Germany.
Jerzy-Roch NoferCentral Laboratory Facility, University Hospital Münster, Albert-Schweitzer- Campus 1, 48149, Münster, Germany.
Hans VinkGlycocalyx Research Institute, Alpine, USA.
Hermann PavenstädtDepartment of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Philipp Kümpers *Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Alexandros Rovas *Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany. Alexandros.rovas@ukmuenster.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prompt identification of clinical deterioration in emergency department (ED) patients presenting with infection is crucial yet challenging. Microvascular dysfunction has been linked to poor clinical outcome in critically ill patients, but it remains unclear whether its detection can predict clinical deterioration in early sepsis. This study aims to evaluate the utility of quantitative microvascular videomicroscopy for predicting clinical deterioration in patients with suspected sepsis.

methodsIn this prospective observational study, 299 ED patients with suspected infection or sepsis were enrolled, with the addition of 50 healthy volunteers, 14 non-infected ED patients and 34 intensive care unit (ICU) patients with sepsis as controls. All participants underwent sublingual sidestream darkfield videomicroscopy. The GlycoCheck™ software quantified vascular density, perfused boundary region (PBR; inverse marker of endothelial glycocalyx (eGC) thickness), and the Microvascular Health Score (MVHS™), which integrated capillary density and eGC dimensions. The primary outcome was disease progression within the first week, defined as progression from infection to sepsis or increase in SOFA score in septic patients. Secondary outcomes included in-hospital and 90-day mortality, ICU admission, or a composite outcome of progression or in-hospital death.

resultsSublingual videomicroscopy revealed significant differences in all microvascular variables between ED patients, healthy volunteers and control groups, correlating with disease severity. ED patients with disease progression showed lower capillary density, higher PBR, and lower MVHS at baseline than non-progressors. In patients presenting with infection without sepsis, MVHS demonstrated strong predictive discrimination for progression (AUC 0.79, p < 0.0001), outperforming procalcitonin and interleukin-6. An intact microvascular phenotype (high capillary density and low PBR) markedly reduced the risk of disease progression or in-hospital mortality (OR 0.17, p < 0.001), whereas combined glycocalyx damage and reduced capillary density significantly increased risk (OR 2.39, p = 0.01).

conclusionQuantitative sublingual videomicroscopy predicts early disease progression within the first week and stratifies patients with suspected sepsis into high and low-risk groups at ED presentation.

trial registrationClinicaltrials.gov Identifier NCT03126032, Registration Date 20.02.2017.

Indexed as

GlycocalyxMicrovesselsSepsisAdultAgedDisease ProgressionEarly DiagnosisEmergency Service, HospitalFemaleHumansIntensive Care UnitsMaleMicrocirculationMicroscopy, VideoMiddle AgedProspective StudiesCapillary recruitmentEndothelial glycocalyxMicrovascular health scorePerfused boundary regionSepsis

Identifiers

PMID41998704
PMCPMC13154576

What Socratic holds

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LicenceCC BY
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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 Socratic graph.