Evidence map›Paper›PMID 40662482›Full record

ArticlePediatric pulmonology2025

Surfactant Delivery Is Crucial for Enhancing Function of Ex-Vivo Premature Sheep Lungs: A Feasibility Study.

Richard Pasteka, Lisa Hufnagl, Vasil Vodenicharov, Alissa Blessing, Angelika Berger, Michael Wagner, Tobias Werther

Abstract read
In one paragraph

Article in Pediatric pulmonology, 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

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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

7 authors.

Richard PastekaDepartment Life Science Engineering, Competence Centre Medical Engineering & Integrated Healthcare, University of Applied Sciences Technikum Wien, Vienna, Austria.ORCID https://orcid.org/0000-0001-7245-5117
Lisa HufnaglDepartment of Paediatrics and Adolescent Medicine, Comprehensive Centre for Paediatrics, Division of Neonatology, Paediatric Intensive Care and Neuropaediatrics, Medical University of Vienna, Vienna, Austria.
Vasil VodenicharovDepartment Life Science Engineering, Competence Centre Medical Engineering & Integrated Healthcare, University of Applied Sciences Technikum Wien, Vienna, Austria.
Alissa BlessingDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Angelika BergerDepartment of Paediatrics and Adolescent Medicine, Comprehensive Centre for Paediatrics, Division of Neonatology, Paediatric Intensive Care and Neuropaediatrics, Medical University of Vienna, Vienna, Austria.
Michael WagnerDepartment of Paediatrics and Adolescent Medicine, Comprehensive Centre for Paediatrics, Division of Neonatology, Paediatric Intensive Care and Neuropaediatrics, Medical University of Vienna, Vienna, Austria.
Tobias WertherDepartment of Paediatrics and Adolescent Medicine, Comprehensive Centre for Paediatrics, Division of Neonatology, Paediatric Intensive Care and Neuropaediatrics, Medical University of Vienna, Vienna, Austria.

Funding

This study was supported by a research grant from the European Society for Paediatric Research (ESPR) provided to M.W., Grant ID: RGP2022-EPDRG-01/04.
6 · The paper itself

Abstract

aimTo compare effects of bolus and aerosolization surfactant delivery methods and ventilatory support on improving ex-vivo premature sheep lung function.

methodsThe xPULM lung simulator was used with 16 ex-vivo preterm sheep lungs, of which 6 were analyzed in the bolus group and 3 in the aerosol group after excluding 7 lungs that ruptured during the trial. Surfactant (0.5 mL poractant alfa) was administered via bolus injection or aerosolization. Tidal volume (VT) was measured before and after administration at positive end-expiratory pressure (PEEP) levels of 0, 5, 10, and 15 cmH₂O.

resultsSurfactant administration significantly increased VT (presurfactant median VT = 0.21 mL; post-surfactant median VT = 1.03 mL, p < 0.001). There was a trend toward higher median VT with bolus delivery (1.48 mL) compared to aerosolized delivery (0.43 mL) with borderline significance (p = 0.047) between the two delivery methods. High PEEP levels before surfactant delivery caused lung overdistention. Histological analysis revealed minimal lung tissue injury across samples, despite experimental challenges.

conclusionsIn ex-vivo preterm sheep lungs, surfactant delivery is the primary driver of improved lung function, while PEEP has a smaller impact. The xPULM lung simulator enables research during spontaneous breathing while avoiding ethical issues associated with animal models.

Indexed as

Biological ProductsLungPhospholipidsPulmonary SurfactantsAdministration, InhalationAerosolsAnimalsAnimals, NewbornFeasibility StudiesPositive-Pressure RespirationSheepTidal VolumeAerosolsBiological ProductsPhospholipidsporactant alfaPulmonary Surfactants3R principlesaerosolized surfactant deliveryexogenous surfactant therapylung simulatorsneonatal ventilationpreterm lung developmentrespiratory distress syndrome (RDS)

Identifiers

PMID40662482
PMCPMC12261429

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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.