Evidence map›Paper›PMID 33407728›Full record

ArticleCritical care (London, England)2021

Venoarterial extracorporeal membrane oxygenation induces early immune alterations.

Aurélien Frerou, Mathieu Lesouhaitier, Murielle Gregoire, Fabrice Uhel, Arnaud Gacouin, Florian Reizine, Caroline Moreau, Aurélie Loirat, Adel Maamar, Nicolas Nesseler and 8 more

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Heart-gut interaction in veno-arterial extracorporeal membrane oxygenation: a forgotten axis in critical care perfusion.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Which antimicrobial treatment for patients with bloodstream infection during ECMO support?European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Observational
  11. Article
  12. Review
  13. Research progress on the pathogenesis of AKI complicated by ECMO.Clinical and experimental nephrology · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

18 authors at 2 institutions in 1 country.

Aurélien FrerouMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Mathieu LesouhaitierMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Murielle GregoireINSERM, EFS Bretagne, UMR U1236, Université de Rennes 1, 35000, Rennes, France.
Fabrice UhelMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Arnaud GacouinMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Florian ReizineMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Caroline MoreauService de Bactériologie, CHU Rennes, 35033, Rennes, France.
Aurélie LoiratService de Cardiologie et maladies vasculaires, CHU de Rennes, 35033, Rennes, France.
Adel MaamarMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Nicolas NesselerAnesthésie-Réanimation, CHU Rennes, 35033, Rennes, France.
Amedeo AnselmiChirurgie Cardio-Thoracique Et Vasculaire, CHU Rennes, 35033, Rennes, France.
Erwan FlecherChirurgie Cardio-Thoracique Et Vasculaire, CHU Rennes, 35033, Rennes, France.
Jean-Philippe VerhoyeChirurgie Cardio-Thoracique Et Vasculaire, CHU Rennes, 35033, Rennes, France.
Yves Le TulzoMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France.
Michel CognéINSERM, EFS Bretagne, UMR U1236, Université de Rennes 1, 35000, Rennes, France.
Mikael RousselINSERM, EFS Bretagne, UMR U1236, Université de Rennes 1, 35000, Rennes, France.
Karin TarteINSERM, EFS Bretagne, UMR U1236, Université de Rennes 1, 35000, Rennes, France.
Jean-Marc TadiéMaladies Infectieuses Et Réanimation Médicale, CHU Rennes, 35033, Rennes, France. jeanmarc.tadie@chu-rennes.fr.ORCID 0000-0002-7604-4849
Centre Hospitalier Universitaire de Rennes · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVenoarterial extracorporeal membrane oxygenation (VA-ECMO) provides heart mechanical support in critically ill patients with cardiogenic shock. Despite important progresses in the management of patients under VA-ECMO, acquired infections remain extremely frequent and increase mortality rate. Since immune dysfunctions have been described in both critically ill patients and after surgery with cardiopulmonary bypass, VA-ECMO initiation may be responsible for immune alterations that may expose patients to nosocomial infections (NI). Therefore, in this prospective study, we aimed to study immune alterations induced within the first days by VA-ECMO initiation.

methodsWe studied immune alterations induced by VA-ECMO initiation using cytometry analysis to characterize immune cell changes and enzyme-linked immunosorbent assay (ELISA) to explore plasma cytokine levels. To analyze specific changes induced by VA-ECMO initiation, nine patients under VA-ECMO (VA-ECMO patients) were compared to nine patients with cardiogenic shock (control patients).

resultsBaseline immune parameters were similar between the two groups. VA-ECMO was associated with a significant increase in circulating immature neutrophils with a significant decrease in C5a receptor expression. Furthermore, we found that VA-ECMO initiation was followed by lymphocyte dysfunction along with myeloid-derived suppressor cells (MDSC) expansion. ELISA analysis revealed that VA-ECMO initiation was followed by an increase in pro-inflammatory cytokines such as IL-6, IL-8 and TNF-α along with IL-10, a highly immunosuppressive cytokine.

conclusionVA-ECMO is associated with early immune changes that may be responsible for innate and adaptive immune alterations that could confer an increased risk of infection.

Indexed as

AgedChi-Square DistributionCytokinesExtracorporeal Membrane OxygenationFemaleHumansImmune System DiseasesMaleMiddle AgedProspective StudiesShock, CardiogenicStatistics, NonparametricCytokinesAcquired infectionsImmunosuppressionLymphocyte exhaustionLymphopeniaMDSCVA-ECMO

Identifiers

PMID33407728
PMCPMC7788860
OpenAlexW3118783530

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.