Publication:
Comparison of Oropharyngeal Leak Pressure Between the Sacovlm™ Video Laryngeal Mask and LMA Supreme in Adult Elective Surgery Patients: A Prospective Randomized Controlled Trial

dc.authorwosidDost, Burhan/Aas-4788-2020
dc.authorwosidUstun, Yasemin/Hke-8711-2023
dc.authorwosidTurunc, Esra/Jwa-2584-2024
dc.authorwosidBilgin, Sezgin/Luz-6903-2024
dc.contributor.authorOzden, Gaye Gamze
dc.contributor.authorDost, Burhan
dc.contributor.authorKaya, Cengiz
dc.contributor.authorTurunc, Esra
dc.contributor.authorKoksal, Ersin
dc.contributor.authorUstun, Yasemin Burcu
dc.contributor.authorBaris, Sibel
dc.date.accessioned2025-12-11T00:47:48Z
dc.date.issued2025
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Ozden, Gaye Gamze; Dost, Burhan; Kaya, Cengiz; Turunc, Esra; Koksal, Ersin; Ustun, Yasemin Burcu; Bilgin, Sezgin; Baris, Sibel] Ondokuz Mayis Univ, Fac Med, Dept Anesthesiol & Reanimat, Samsun, Turkiyeen_US
dc.description.abstractBackground This study aimed to compare the oropharyngeal leak pressure (OLP) of SaCoVLM (TM) with that of LMA Supreme. Methods This prospective, randomized, controlled, single-blind study enrolled patients aged 18-80 years with American Society of Anesthesiologists physical status of classes I and II. The OLP was the primary outcome measure of the study. The glottic visualization grades, laryngeal mask insertion time and number of attempts, requirement for additional maneuvers, and incidence of complications were the secondary outcome measures. Results A total of 168 patients, comprising 83 patients in the SaCoVLM (TM) group and 85 patients in the LMA Supreme group, were included in this study. The median OLP values were 27 [24.0-30.0] cmH(2)O and 25 [20.0-35.0] cmH2O in the SaCoVLM (TM) and LMA Supreme groups, respectively. No significant differences were observed between the groups in terms of the OLP (p > 0.05). The first-attempt success rate in the SaCoVLM (TM) group was significantly higher than that in the LMA supreme group (98.8% vs. 91.8%, p = 0.034). In terms of glottic assessment, the complete glotis visualization rate in the SaCoVLM (TM) group (p < 0.001) was significantly higher than that in the LMA supreme group. However, the Grade 1-3 visualization rates were significantly lower in the SaCoVLM (TM) group (p < 0.001). Complications such as mucosal damage and postoperative sore throat were observed more frequently in the LMA Supreme group (p = 0.001). Conclusions SaCoVLM (TM), which offers comparable OLP, superior glottic visualization, high first-attempt success rates, and a lower incidence of complications, may serve as an alternative supraglottic airway device. Trial registration The study was registered on ClinicalTrials.gov (Identifier: NCT06245668).en_US
dc.description.sponsorshipCommission Presidency of Scientific Research Projects of Ondokuz Mayis University, Samsun, Turkey [BAP04-B-2023-4862]en_US
dc.description.sponsorshipThis study was supported by the Commission Presidency of Scientific Research Projects of Ondokuz Mayis University, Samsun, Turkey, under project number BAP04-B-2023-4862.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1186/s12871-025-03218-4
dc.identifier.issn1471-2253
dc.identifier.issue1en_US
dc.identifier.pmid40610857
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.1186/s12871-025-03218-4
dc.identifier.urihttps://hdl.handle.net/20.500.12712/39318
dc.identifier.volume25en_US
dc.identifier.wosWOS:001523058500001
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherBMCen_US
dc.relation.ispartofBMC Anesthesiologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAdulten_US
dc.subjectAirway Managementen_US
dc.subjectAnesthetic Complicationen_US
dc.subjectBronchoscopyen_US
dc.subjectGeneral Anesthesiaen_US
dc.subjectLaryngeal Masksen_US
dc.titleComparison of Oropharyngeal Leak Pressure Between the Sacovlm™ Video Laryngeal Mask and LMA Supreme in Adult Elective Surgery Patients: A Prospective Randomized Controlled Trialen_US
dc.typeArticleen_US
dspace.entity.typePublication

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