Evidence map›Paper›PMID 41968311›Full record

ArticleCritical care (London, England)2026

Full percutaneous decannulation of VA-ECMO using MANTA

Elodie Berg, Charles Juvin, Marc Pineton De Chambrun, Charifa Nazoiri, Nathalie Nardone, Pichoy Danial, Cosimo D'Alessandro, Aude Carillion, Alain Combes, Pascal Leprince and 2 more

Abstract read
In one paragraph

Article in Critical care (London, England), 2026. 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

12 authors.

Elodie BergDepartment of Cardio-Thoracic Surgery, Pitié-Salpêtrière Hospital, Paris, France. elodie.berg@aphp.fr.
Charles JuvinDepartment of Cardio-Thoracic Surgery, Pitié-Salpêtrière Hospital, Paris, France.
Marc Pineton De ChambrunMedical Intensive Care Unit, Pitié-Salpêtrière Hospital, Paris, France.
Charifa NazoiriDepartment of Public Health, Pitié-Salpêtrière Hospital, Paris, France.
Nathalie NardoneDepartement of Cardio-thoracic Surgery, Rouen Hospital, Rouen, France.
Pichoy DanialDepartment of Cardio-Thoracic Surgery, Pitié-Salpêtrière Hospital, Paris, France.
Cosimo D'AlessandroDepartment of Cardio-Thoracic Surgery, Pitié-Salpêtrière Hospital, Paris, France.
Aude CarillionDMU DREAM, Department of Anesthesiology and Critical Care, Sorbonne university, Pitié-Salpêtrière Hospital, Paris, France.
Alain CombesMedical Intensive Care Unit, Pitié-Salpêtrière Hospital, Paris, France.
Pascal LeprinceDepartment of Cardio-Thoracic Surgery, Pitié-Salpêtrière Hospital, Paris, France.
Adrien BougleDMU DREAM, Department of Anesthesiology and Critical Care, Sorbonne university, Pitié-Salpêtrière Hospital, Paris, France.
Guillaume LebretonDepartment of Cardio-Thoracic Surgery, Pitié-Salpêtrière Hospital, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPercutaneous veno-arterial extracorporeal membrane oxygenation (VA-ECMO) implantation reduces infectious complications compared with surgical cannulation. However, arterial decannulation using manual compression remains associated with bleeding, vascular injury, and infection. We evaluated a fully percutaneous decannulation strategy (FP-D) combining MANTA® and Femoseal® devices.

methodsAll patients undergoing FP-D between October 2020 and May 2022 in our institution were included. Outcomes were compared with a historical cohort decannulated using manual compression (MC). The primary endpoint was surgical revision after decannulation. Secondary endpoints included major bleeding, transfusion, vascular complications, infection, and 30-day survival. A propensity score weighting approach was performed to adjust for baseline differences.

resultsAmong 497 patients treated with percutaneous VA-ECMO, 250 underwent FP-D and 247 MC. After propensity score, FP-D significantly reduced surgical revision (3.9% vs. 7.2%; RR 0.55, 95% CI 0.32–0.94; p = 0.0311), infection requiring surgery (3.7% vs. 8.4%; RR 0.44, 95% CI 0.25–0.77; p = 0.004), and major bleeding (1.4% vs. 11%; RR 0.13, 95% CI 0.06–0.30; p < 0.0001), with lower transfusion requirements (7.1% vs. 45.7%; RR 0.16, 95% CI 0.11–0.22; p < 0.0001). Thirty-day death was comparable between groups (8,2% vs. 5,57%; p = 0.1316). Systematic CT scans revealed frequent but mostly silent arterial lesions after FP-D.

conclusionFP-D markedly reduced bleeding, transfusion, infection, and surgical revision compared with manual compression, while preserving short-term survival. Systematic imaging identified frequent subclinical vascular lesions, supporting targeted surveillance and endovascular management when appropriate.

Indexed as

Device RemovalExtracorporeal Membrane OxygenationAgedFemaleHumansMaleMiddle AgedPropensity ScoreRetrospective StudiesComplicationsDecannulationExtracorporeal Membrane OxygenationHemostasisVascular Closure Devices

Identifiers

PMID41968311
PMCPMC13185302

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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.