Evidence map›Paper›PMID 41039946›Full record

Trial reportAnaesthesiology intensive therapy2025

Comparison of LTS-D and i-gel in non-paralyzed pediatric patients under general anesthesia: a randomized trial.

Mostafa Somri, Feras Somri, Luis Gaitini, Anan Safadi, Ayoub Abd El Azim, Ibraheem Mafra, Manuel Ángel Gómez-Ríos

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Anaesthesiology intensive therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mostafa SomriDepartment of Anesthesia, Bnai Zion Medical Center, Haifa, Israel.
Feras SomriFaculty of Medicine, D'Annunzio University of Chieti-Pescara, Italy.
Luis GaitiniDepartment of Anesthesia, Bnai Zion Medical Center, Haifa, Israel.
Anan SafadiDepartment of Anesthesia, Bnai Zion Medical Center, Haifa, Israel.
Ayoub Abd El AzimDepartment of Anesthesia, Bnai Zion Medical Center, Haifa, Israel.
Ibraheem MafraDepartment of Anesthesia, Bnai Zion Medical Center, Haifa, Israel.
Manuel Ángel Gómez-RíosDepartment of Anesthesiology and Perioperative Medicine, University Hospital Complex of A Coruña, A Coruña, Galicia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSecond-generation supraglottic airway devices, such as the laryngeal tube suction disposable (LTS-D) and i-gel, are widely used in pediatric anesthesia due to advantages such as improved sealing and gastric drainage. This randomized controlled trial compared the efficacy and safety of the LTS-D and i-gel in non-paralyzed pediatric patients under general anesthesia. MATERIAL AND

methodsEighty ASA I children aged 2-8 years (12-25 kg), scheduled for short elective surgical procedures, were randomized to the LTS-D (n = 40) or i-gel (n = 40) group. Primary outcomes were oxygen saturation (SpO₂) and end-tidal CO₂ (EtCO₂). Secondary outcomes included insertion time, oropharyngeal leak pressure, fiberoptic view, tidal volumes (Vt), and adverse events.

resultsBoth devices maintained comparable oxygenation. Mean EtCO₂ was slightly higher in the i-gel group, with a mean difference of 2.56 mmHg (95% CI: 1.86-3.26; P < 0.001). The i-gel had significantly faster insertion times (24.53 ± 2.00 s vs. 31.20 ± 1.95 s; P < 0.001) and superior fiberoptic visualization (optimal grades in 99% vs. 70%; P < 0.001). The LTS-D showed higher oropharyngeal leak pressures (37.63 ± 3.71 cmH₂O vs. 24.43 ± 1.72 cmH₂O; P < 0.001). Vt and adverse event rates were similar, with no severe complications reported (P = 0.65).

conclusionsBoth the LTS-D and i-gel are safe and effective for airway management in non-paralyzed children undergoing short procedures. The i-gel enables faster insertion and better anatomical positioning, while the LTS-D offers higher leak pressures, making it preferable when a better seal is needed. Device choice should be guided by clinical context and patient characteristics.

Indexed as

Airway ManagementAnesthesia, GeneralIntubation, IntratrachealLaryngeal MasksCarbon DioxideChildChild, PreschoolFemaleHumansMaleOxygen SaturationTidal VolumeCarbon Dioxideairway managementi-gellaryngeal tube suction disposablepediatric anesthesiarandomized controlled trialsupraglottic airway devices

Identifiers

PMID41039946
PMCPMC12793976

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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.