Evidence map›Paper›PMID 42096041›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2026

Kinetics of Sevoflurane Vaporized Directly in Extracorporeal Membrane Oxygenators-Ex Vivo Findings and Pharmacokinetic/Pharmacodynamic Simulations.

Diana Morales Castro, Mark Alm, Federico Carlos Carini, Courtney Fischer, Georgiana Roman-Sarita, Linda Dresser, John Granton, Eric Chen, Kiran Shekar, Eddy Fan

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Article in European journal of drug metabolism and pharmacokinetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Diana Morales CastroInterdepartmental Division of Critical Care Medicine, Toronto General Hospital, University of Toronto, 585 University Avenue, 9-MaRS-9013, Toronto, ON, M5G 2N2, Canada. diana.moralescastro@uhn.ca.ORCID http://orcid.org/0000-0001-9205-9613
Mark AlmDepartment of Perfusion Services, Toronto General Hospital, Toronto, Canada.
Federico Carlos CariniIntensive Care Unit, Hospital Italiano, Buenos Aires, Argentina.
Courtney FischerDepartment of Perfusion Services, Toronto General Hospital, Toronto, Canada.
Georgiana Roman-SaritaDepartment of Respiratory Therapy, Toronto General Hospital, Toronto, Canada.
Linda DresserLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
John GrantonInterdepartmental Division of Critical Care Medicine, Toronto General Hospital, University of Toronto, 585 University Avenue, 9-MaRS-9013, Toronto, ON, M5G 2N2, Canada.
Eric ChenLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Kiran ShekarAdult Intensive Care Services, The Prince Charles Hospital, Brisbane, Australia.
Eddy FanInterdepartmental Division of Critical Care Medicine, Toronto General Hospital, University of Toronto, 585 University Avenue, 9-MaRS-9013, Toronto, ON, M5G 2N2, Canada.

Funding

Physicians' Services Incorporated Foundation 22-37
6 · The paper itself

Abstract

backgroundAlthough sedation is commonly used in patients undergoing venovenous extracorporeal membrane oxygenation (V-V ECMO), the use of volatile anesthetics is less frequent, and there is limited data on the pharmacokinetics/pharmacodynamics (PK/PD) of these sedatives (e.g., sevoflurane) directly vaporized into ECMO circuits. We aimed to develop a kinetic model for sevoflurane vaporized in ex vivo ECMO oxygenators to inform the design of a pilot clinical trial to evaluate the safety, feasibility, and in vivo PK/PD model of such a strategy in patients supported with V-V ECMO.

methodsWe conducted ex vivo trials using three ECMO circuits primed with Ringer's lactate, and the ECMO pump speed set to achieve a fluid flow rate of 5 L/min. Sevoflurane was vaporized at concentrations of 1-8% with sweep gas flow (SGF) rates of 1-10 L/min. We analyzed sevoflurane concentrations in the ECMO circuit using headspace gas chromatography-mass spectrometry and monitored environmental sevoflurane concentrations for safety. We used sequential PK/PD modeling to simulate clinical conditions, targeting sedation levels defined by processed electroencephalography (Patient State Index [PSI] 40-60), using pharmacodynamic parameters derived from non-ECMO populations.

resultsSevoflurane effectively crossed polymethyl pentene (PMP) membranes, rapidly reaching maximum concentrations (C

conclusionsOur ex vivo findings demonstrate the feasibility of using sevoflurane vaporized directly into ECMO circuits as a sedative strategy. These results provide a robust foundation for translating this delivery strategy into a pilot clinical trial aimed at optimizing ECMO sedation with inhaled sevoflurane in patients with severe ARDS.

Indexed as

Anesthetics, InhalationExtracorporeal Membrane OxygenationHypnotics and SedativesSevofluraneHumansMaleModels, BiologicalOxygenators, MembranePilot ProjectsVolatilizationAnesthetics, InhalationHypnotics and SedativesSevoflurane

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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.