Evidence map›Paper›PMID 33861804›Full record

Observational studyPloS one2021

CT-based determination of excessive visceral adipose tissue is associated with an impaired survival in critically ill patients.

Theresa H Wirtz, Sven H Loosen, Maximilian Schulze-Hagen, Ralf Weiskirchen, Lukas Buendgens, Samira Abu Jhaisha, Jonathan F Brozat, Tobias Puengel, Mihael Vucur, Pia Paffenholz and 6 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-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.

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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

16 authors at 4 institutions in 1 country.

Theresa H WirtzDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0003-2778-2447
Sven H LoosenClinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Maximilian Schulze-HagenDepartment of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Aachen, Germany.
Ralf WeiskirchenInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0003-3888-0931
Lukas BuendgensDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Samira Abu JhaishaDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Jonathan F BrozatDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Tobias PuengelDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Mihael VucurClinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Pia PaffenholzDepartment of Urology, University Hospital Cologne, Cologne, Germany.
Christiane KuhlDepartment of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Aachen, Germany.
Frank TackeDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Berlin, Germany.
Christian TrautweinDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Tom LueddeClinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Christoph RoderburgDepartment of Hepatology and Gastroenterology, Charité University Medicine Berlin, Berlin, Germany.
Alexander KochDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
RWTH Aachen University · DECharité - Universitätsmedizin Berlin · DEDüsseldorf University Hospital · DEUniversity Hospital Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveObesity is a negative prognostic factor for various clinical conditions. In this observational cohort study, we evaluated a CT-based assessment of the adipose tissue distribution as a potential non-invasive prognostic parameter in critical illness.

methodsRoutine CT-scans upon admission to the intensive care unit (ICU) were used to analyze the visceral and subcutaneous adipose tissue areas at the 3rd lumbar vertebra in 155 patients. Results were correlated with various prognostic markers and both short-term- and overall survival. Multiple statistical tools were used for data analysis.

resultsWe observed a significantly larger visceral adipose tissue area in septic patients compared to non-sepsis patients. Interestingly, patients requiring mechanical ventilation had a significantly higher amount of visceral adipose tissue correlating with the duration of mechanical ventilation. Moreover, both visceral and subcutaneous adipose tissue area significantly correlated with several laboratory markers. While neither the visceral nor the subcutaneous adipose tissue area was predictive for short-term ICU survival, patients with a visceral adipose tissue area above the optimal cut-off (241.4 cm2) had a significantly impaired overall survival compared to patients with a lower visceral adipose tissue area.

conclusionsOur study supports a prognostic role of the individual adipose tissue distribution in critically ill patients. However, additional investigations need to confirm our suggestion that routine CT-based assessment of adipose tissue distribution can be used to yield further information on the patients' clinical course. Moreover, future studies should address functional and metabolic analysis of different adipose tissue compartments in critical illness.

Indexed as

Abdominal FatAdultAgedAged, 80 and overCohort StudiesCritical IllnessHumansIntensive Care UnitsMaleMiddle AgedObesitySubcutaneous FatTomography, X-Ray ComputedYoung Adult

Identifiers

PMID33861804
PMCPMC8051769
OpenAlexW3156028417

What OpenQuestion holds

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Registered trials

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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.