Evidence map›Paper›PMID 40180673›Full record

ArticleAnnals of intensive care2025

Does Levosimendan hasten veno-arterial ECMO weaning? A propensity score matching analysis.

Nicolas Paulo, Antoine Kimmoun, David Hajage, Pierre Hubert, David Levy, Marc Pineton de Chambrun, Juliette Chommeloux, Ouriel Saura, Grégoire Del Marmol, Quentin Moyon and 7 more

Abstract read
In one paragraph

Article in Annals of intensive care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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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

17 authors.

Nicolas PauloAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Antoine KimmounInstitut Lorrain du Cœur Et Des Vaisseaux, Service de Médecine Intensive-Réanimation, FCRIN-INICRCT, Université de Lorraine, CHRU de Nancy, U1116, Nancy, France.
David HajageDépartement Biostatistique Santé Publique Et Information Médicale, Centre de Pharmacoépidémiologie (Cephepi), Sorbonne Université, AP-HP, Hôpital Pitié-Salpêtrière, Unité de Recherche Clinique PSL-CFX, CIC-1421, Paris, France.
Pierre HubertInstitut Lorrain du Cœur Et Des Vaisseaux, Service de Médecine Intensive-Réanimation, FCRIN-INICRCT, Université de Lorraine, CHRU de Nancy, U1116, Nancy, France.
David LevyAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Marc Pineton de ChambrunAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Juliette ChommelouxAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Ouriel SauraAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Grégoire Del MarmolAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Quentin MoyonAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Guillaume HékimianAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Melchior GautierAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Charles Edouard LuytAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Guillaume LebretonInstitute of Cardiometabolism and Nutrition, Sorbonne Université, UMRS_1166-ICAN75013, Paris, France.
Bruno LevyInstitut Lorrain du Cœur Et Des Vaisseaux, Service de Médecine Intensive-Réanimation, FCRIN-INICRCT, Université de Lorraine, CHRU de Nancy, U1116, Nancy, France.
Alain CombesAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.
Matthieu SchmidtAP-HP, Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France. matthieu.schmidt@aphp.fr.ORCID http://orcid.org/0000-0002-2931-4412

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreliminary evidence from small, single-center studies suggests levosimendan may improve the likelihood of successful venoarterial extracorporeal membrane oxygenation (VA-ECMO) weaning in patients with cardiogenic shock. However, the literature is limited and presents conflicting results. We aimed to assess the benefits of levosimendan on VA-ECMO for time to successful ECMO weaning, using a pragmatic and rigorous definition of successful VA-ECMO weaning in patients with potential for cardiac function recovery.

methodsA retrospective bicentric study over 6 years was conducted, including patients who received levosimendan during their ECMO course. Patients with post-cardiotomy cardiogenic shock or end-stage chronic heart failure were excluded. Patients receiving levosimendan while on VA-ECMO were matched to those not receiving levosimendan during the same period, based on pre-specified variables and time from ECMO initiation. The primary endpoint was successful VA-ECMO weaning, defined as survival without death, heart transplantation, or LVAD within 30 days after VA-ECMO withdrawal.

resultsOver the study period, 320 patients treated with VA-ECMO for refractory cardiogenic shock were included, of whom 68 received levosimendan during their ECMO course. Propensity score matching yielded 47 unique pairs of patients with comparable characteristics. After matching, successful ECMO weaning was achieved in 16 out of 47 patients (34%) in the no-levosimendan group and 21 out of 47 patients (45%) in the levosimendan group (sHR, 1.45 [95% CI, 0.77-2.70]; P = 0.25). Similarly, there were no significant differences between the groups in terms of bridge-to-heart transplant, LVAD, or death. Left ventricular ejection fraction and aortic velocity time integral improved significantly after levosimendan in all patients, regardless of their VA-ECMO weaning status.

conclusionIn patients with non-postoperative cardiogenic shock supported by peripheral VA-ECMO, levosimendan was not associated with increased rates of successful VA-ECMO weaning or improved 30-day and 6-month bridge-free survival. Results from double-blinded randomized controlled trials are urgently needed to clarify the effectiveness and optimal timing of levosimendan in this specific population.

Indexed as

Cardiogenic shock—mechanical circulatory supportECMO weaningExtracorporeal membrane oxygenationLevosimendan

Identifiers

PMID40180673
PMCPMC11968594

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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.