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dc.contributorHospital General de Granollers
dc.contributor.authorRognoni, Gina
dc.contributor.authorGarcía, Carolina
dc.contributor.authorCabañes, Sara
dc.contributor.authorde la Torre, Maria
dc.contributor.authorPedrós, Cristina
dc.contributor.authorSubira, Carles
dc.contributor.authorbaquerizo vargas, herbert glenny
dc.date.accessioned2024-08-30T07:46:42Z
dc.date.available2024-08-30T07:46:42Z
dc.date.issued2024-07-16
dc.identifier.citationSubirà C, Rognoni G, Baquerizo H, García C, Cabañes S, de la Torre M, et al. Effect of lung volume preservation during spontaneous breathing trial on successful extubation in patients receiving mechanical ventilation: protocol for a multicenter clinical trial. Trials. 2024 Jul 16;25(1):481.
dc.identifier.issn1745-6215
dc.identifier.urihttps://hdl.handle.net/11351/11887
dc.descriptionExtubation; Lung ultrasound; Mechanical ventilation
dc.description.abstractBackground: In standard weaning from mechanical ventilation, a successful spontaneous breathing test (SBT) consisting of 30 min 8 cmH2O pressure-support ventilation (PSV8) without positive end-expiratory pressure (PEEP) is followed by extubation with continuous suctioning; however, these practices might promote derecruitment. Evidence supports the feasibility and safety of extubation without suctioning. Ultrasound can assess lung aeration and respiratory muscles. We hypothesize that weaning aiming to preserve lung volume can yield higher rates of successful extubation. Methods: This multicenter superiority trial will randomly assign eligible patients to receive either standard weaning [SBT: 30-min PSV8 without PEEP followed by extubation with continuous suctioning] or lung-volume-preservation weaning [SBT: 30-min PSV8 + 5 cmH2O PEEP followed by extubation with positive pressure without suctioning]. We will compare the rates of successful extubation and reintubation, ICU and hospital stays, and ultrasound measurements of the volume of aerated lung (modified lung ultrasound score), diaphragm and intercostal muscle thickness, and thickening fraction before and after successful or failed SBT. Patients will be followed for 90 days after randomization. Discussion: We aim to recruit a large sample of representative patients (N = 1600). Our study cannot elucidate the specific effects of PEEP during SBT and of positive pressure during extubation; the results will show the joint effects derived from the synergy of these two factors. Although universal ultrasound monitoring of lungs, diaphragm, and intercostal muscles throughout weaning is unfeasible, if derecruitment is a major cause of weaning failure, ultrasound may help clinicians decide about extubation in high-risk and borderline patients.
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofseriesTrials;25(1)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectPulmons - Ecografia
dc.subjectRespiració artificial
dc.subjectAssaigs clínics
dc.subject.meshRespiration, Artificial
dc.subject.meshAirway Extubation
dc.subject.meshClinical Trial
dc.titleEffect of lung volume preservation during spontaneous breathing trial on successful extubation in patients receiving mechanical ventilation: protocol for a multicenter clinical trial
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1186/s13063-024-08297-1
dc.subject.decsrespiración artificial
dc.subject.decsextubación de la vía aérea
dc.subject.decsensayo clínico
dc.relation.publishversionhttps://doi.org/10.1186/s13063-024-08297-1
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Subirà C] Servei de Medicina Intensiva, Hospital de La Santa Creu I Sant Pau, Barcelona, Spain. Grup de Recerca en Malalt Crític (GMC), Institut de Recerca I Innovació en Ciències de La Vida I de La Salut a La Catalunya Central (IRIS-CC), Vic, Spain. CIBER Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain. Servei de Medicina Intensiva, Althaia Xarxa Assistencial Universitària de Manresa, Manresa, Spain. [Rognoni G, Baquerizo H] Grup de Recerca en Malalt Crític (GMC), Institut de Recerca I Innovació en Ciències de La Vida I de La Salut a La Catalunya Central (IRIS-CC), Vic, Spain. Servei de Medicina Intensiva, Althaia Xarxa Assistencial Universitària de Manresa, Manresa, Spain. Programa de Doctorat en Medicina I Ciències Biomèdiques, Universitat de Vic- Universitat Central de Catalunya (UVIC-UCC), Vic, Spain. [García C] Servicio de Medicina Intensiva, Hospital Universitario de Canarias, San Cristóbal de La Laguna, Tenerife, Spain. [Cabañes S] Servicio de Medicina Intensiva, Txagorritxu Hospital Universitario Araba, Gasteiz, Spain. [de la Torre M] Servei de Medicina Intensiva, Hospital de Mataró, Mataró, Spain. [Pedrós C] Servei de Medicina Intensiva, Hospital General de Granollers, Granollers, Spain
dc.identifier.pmid39014430
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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