Evidence map›Paper›PMID 40038820›Full record

Trial reportCritical care (London, England)2025

Alterations in the lipid profile of critically ill children in relation to outcome.

Lauren De Bruyn, Sarah Vander Perre, Sascha Verbruggen, Koen Joosten, Greet Van den Berghe, Lies Langouche

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Critical care (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Lauren De BruynClinical Division and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1 Box 503, 3000, Leuven, Belgium.ORCID http://orcid.org/0000-0002-5036-3403
Sarah Vander PerreClinical Division and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1 Box 503, 3000, Leuven, Belgium.
Sascha VerbruggenIntensive Care Unit, Department of Neonatal and Paediatric Intensive Care, Division of Pediatric Intensive Care, Erasmus Medical Centre-Sophia Children's Hospital, Rotterdam, Netherlands.ORCID http://orcid.org/0000-0003-4866-9865
Koen JoostenIntensive Care Unit, Department of Neonatal and Paediatric Intensive Care, Division of Pediatric Intensive Care, Erasmus Medical Centre-Sophia Children's Hospital, Rotterdam, Netherlands.ORCID http://orcid.org/0000-0002-0504-2475
Greet Van den BergheClinical Division and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1 Box 503, 3000, Leuven, Belgium.ORCID http://orcid.org/0000-0002-5320-1362
Lies LangoucheClinical Division and Laboratory of Intensive Care Medicine, Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, O&N1 Box 503, 3000, Leuven, Belgium. lies.langouche@kuleuven.be.ORCID http://orcid.org/0000-0002-8564-6809

Funding

Fonds Wetenschappelijk Onderzoek G069421NH2020 European Research Council ERC-2023-ADG-101133276Methusalem program of the Flemish Government METH/14/06
6 · The paper itself

Abstract

backgroundCritically ill adults typically develop hypocholesterolemia, associated with poor outcome. Whether similar alterations occur in critically ill children is less clear.

methodsIn secondary analyses of the PEPaNIC RCT (n = 1440), we first documented the time course of plasma cholesterol and triglyceride concentrations, and the effect of randomization to early-parenteral-nutrition (early-PN) or late-PN hereon, for 96 matched critically ill children staying ≥ 5 days in PICU. Second, for 1165 children with available admission plasma samples, lipid profiles were determined and their independent associations with outcome (time to live PICU discharge, new infection and 90-day mortality) were assessed with Multivariable Cox proportional hazard and logistic regression, adjusting for baseline risk factors.

resultsPlasma HDL-cholesterol, LDL-cholesterol, total-cholesterol and triglycerides were low throughout the 5 PICU days, with only HDL-cholesterol further decreasing over time (P < 0.0001) and without effect of randomization to early-PN or late-PN, and with admission values lower in infants than older children and in patients with infection (P < 0.05). Lower admission HDL- and total-cholesterol concentrations were independently associated with a lower likelihood of an earlier live PICU discharge (P < 0.001) and with a higher risk of 90-day mortality (P ≤ 0.01), whereas higher plasma triglycerides were independently associated with higher risk of 90-day mortality (P = 0.004). Low admission plasma HDL-cholesterol was independently associated with a higher risk of acquiring a new infection (P = 0.05).

conclusionCritically ill children presented with low circulating levels of lipids. Low plasma cholesterol concentrations were associated with poor outcomes, most robustly for HDL-cholesterol. Whether these associations are causal or casual requires further investigation.

Indexed as

Critical IllnessLipidsAdolescentChildChild, PreschoolCholesterolCholesterol, HDLFemaleHumansInfantIntensive Care Units, PediatricMaleParenteral NutritionTriglyceridesCholesterolCholesterol, HDLLipidsTriglyceridesHypocholesterolemiaIntensive careParenteral nutritionPediatricTriglyceride

Identifiers

PMID40038820
PMCPMC11881302

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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.