Evidence map›Paper›PMID 39324447›Full record

ArticleActa obstetricia et gynecologica Scandinavica2024

How does fetal inflammatory response syndrome change fetal response to hypoxia? An experimental study in a fetal sheep model.

Geoffroy Chevalier, Charles Garabedian, Valeria De Stephano, Anne Wojtanowski, Yasmine Ould Hamoud, Louis Galan, Dyuti Sharma, Kevin Le Duc, Julien De Jonckheere, Laurent Storme and 2 more

Abstract read
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2024. 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

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

3 citing papers in PubMed.

  1. Trial
  2. Article
  3. 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.

Geoffroy ChevalierULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.ORCID 0000-0003-4901-9354
Charles GarabedianULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Valeria De StephanoULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Anne WojtanowskiCIC-IT 1403, CHU Lille, Lille, France.ORCID 0009-0008-2237-6259
Yasmine Ould HamoudDepartment of Obstetrics, CHU Lille, Lille, France.
Louis GalanULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Dyuti SharmaULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Kevin Le DucULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Julien De JonckheereULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Laurent StormeULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Guillemette MarotULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.
Louise GhesquièreULR 2694-METRICS-Evaluation des technologies de santé et des pratiques médicales, CHU Lille, Université Lille, Lille, France.ORCID 0000-0003-4142-5526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFetal inflammatory response syndrome associated with acidosis during labor is a high-risk situation for the fetus. This study evaluated hemodynamic, gasometric, and heart rate variability changes during acute fetal inflammatory response syndrome associated with hypoxia, compared with isolated hypoxia. MATERIAL AND

methodsAcute fetal inflammatory response syndrome was obtained via an intravenously injection of lipopolysaccharide derived from Escherichia coli. Hypoxia was induced by repeated umbilical cord occlusions during three phases: mild, moderate, and severe umbilical cord occlusions. Two groups were created with chronically instrumented near-term fetal sheep: one group with isolated hypoxia, the other with hypoxia and fetal inflammatory response syndrome. Hemodynamic, gas parameters, and fetal heart rate variability were compared between the groups.

resultsThe hypoxia and fetal inflammatory response syndrome group had a higher mortality rate (n = 4/9) compared with the hypoxia group (n = 0/9). Gasometric state was altered earlier in case of lipopolysaccharide injection (pH = 7.22 (7.12-7.24) vs 7.28 (7.23-7.34) p = 0.01; lactate = 10.3 mmol/L (9.4-11.0) vs 6.0 mmol/L (4.1-8.2) p < 0.001 after mild occlusions). After mild occlusions, the hypoxia and fetal inflammatory response syndrome group had higher values on seven heart rate variability parameters compared with the hypoxia group. After moderate occlusions, two parameters remained significantly higher.

conclusionsDuring fetal inflammatory response syndrome, fetal adaptation to hypoxia is impaired. In case of fetal infection, acidosis during labor is likely to become severe more rapidly, requiring closer fetal monitoring during labor.

Indexed as

Fetal HypoxiaHeart Rate, FetalLipopolysaccharidesSystemic Inflammatory Response SyndromeAcidosisAnimalsBlood Gas AnalysisDisease Models, AnimalFemaleHemodynamicsPregnancySheepLipopolysaccharidesfetusFIRSheart rate variabilityhypoxiainflammationlipopolysaccharidemonitoringocclusionsheep

Identifiers

PMID39324447
PMCPMC11502433

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.