Publication:
Protective ventilation with high versus low positive end-expiratory pressure during one-lung ventilation for thoracic surgery (PROTHOR): Study protocol for a randomized controlled trial

dc.contributor.authorT. Kissen_US
dc.contributor.authorJ. Wittensteinen_US
dc.contributor.authorC. Beckeren_US
dc.contributor.authorK. Birren_US
dc.contributor.authorG. Cinnellaen_US
dc.contributor.authorE. Cohenen_US
dc.contributor.authorM. R. El Tahanen_US
dc.contributor.authorL. F. Falcãoen_US
dc.contributor.authorC. Gregorettien_US
dc.contributor.authorM. Granellen_US
dc.contributor.authorT. Hachenbergen_US
dc.contributor.authorM. W. Hollmannen_US
dc.contributor.authorR. Jankovicen_US
dc.contributor.authorW. Karzaien_US
dc.contributor.authorJ. Krassleren_US
dc.contributor.authorT. Loopen_US
dc.contributor.authorM. J. Lickeren_US
dc.contributor.authorN. Marczinen_US
dc.contributor.authorG. H. Millsen_US
dc.contributor.authorM. T. Murrellen_US
dc.contributor.authorV. Neskovicen_US
dc.contributor.authorZ. Nisnevitch-Savareseen_US
dc.contributor.authorP. Pelosien_US
dc.contributor.authorR. Rossainten_US
dc.contributor.authorM. J. Schultzen_US
dc.contributor.authorA. Serpa Netoen_US
dc.contributor.authorP. Severgninien_US
dc.contributor.authorL. Szegedien_US
dc.contributor.authorT. Veghen_US
dc.contributor.authorG. Voyagisen_US
dc.contributor.authorJ. Zhongen_US
dc.contributor.authorM. Gama De Abreuen_US
dc.contributor.authorM. Senturken_US
dc.contributor.otherFudan University Shanghai Cancer Centeren_US
dc.contributor.otherOspedale Policlinico San Martinoen_US
dc.contributor.otherImam Abdulrahman Bin Faisal universityen_US
dc.contributor.otherMedizinische Fakultät und Uniklinikum Magdeburgen_US
dc.contributor.otherUniversity of Nišen_US
dc.contributor.otherVojnomedicinska Akademijaen_US
dc.contributor.otherCentre Hospitalier Universitaire de Charleroien_US
dc.contributor.otherPanepistimion Patronen_US
dc.contributor.otherSotiria General Hospitalen_US
dc.contributor.otherDresden University Faculty of Medicine and University Hospital Carl Gustav Carusen_US
dc.contributor.otherUniversität Freiburg im Breisgauen_US
dc.contributor.otherUniversità degli Studi di Genovaen_US
dc.contributor.otherHarefield Hospitalen_US
dc.contributor.otherSemmelweis Egyetemen_US
dc.contributor.otherUniversità degli Studi di Foggiaen_US
dc.contributor.otherZentralklinik Bad Berkaen_US
dc.contributor.otherUniversità degli Studi di Palermoen_US
dc.contributor.otherHospital Israelita Albert Einsteinen_US
dc.contributor.otherImperial College Londonen_US
dc.contributor.otherUniversidade Federal de Sao Pauloen_US
dc.contributor.otherHospital General Universitario de Valenciaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherIstanbul Üniversitesi Tıp Fakültesien_US
dc.contributor.otherHôpitaux universitaires de Genèveen_US
dc.contributor.otherFudan Universityen_US
dc.contributor.otherUniversità degli Studi dell'Insubriaen_US
dc.contributor.otherThe Mount Sinai Hospitalen_US
dc.contributor.otherDebreceni Egyetemen_US
dc.contributor.otherUniversiteit van Amsterdamen_US
dc.contributor.otherUniversity of Sheffielden_US
dc.contributor.otherAmsterdam UMC - University of Amsterdamen_US
dc.contributor.otherUniklinik RWTH Aachenen_US
dc.contributor.otherThoracic Center Coswigen_US
dc.contributor.otherPenn State Hersheyen_US
dc.contributor.otherOutcomes Research Consortiumen_US
dc.contributor.otherWeill Cornell Medicineen_US
dc.date.accessioned2020-01-27T09:55:17Z
dc.date.available2020-01-27T09:55:17Z
dc.date.issued2019-04-11en_US
dc.description.abstract© 2019 The Author(s). Background: Postoperative pulmonary complications (PPC) may result in longer duration of in-hospital stay and even mortality. Both thoracic surgery and intraoperative mechanical ventilation settings add considerably to the risk of PPC. It is unclear if one-lung ventilation (OLV) for thoracic surgery with a strategy of intraoperative high positive end-expiratory pressure (PEEP) and recruitment maneuvers (RM) reduces PPC, compared to low PEEP without RM. Methods: PROTHOR is an international, multicenter, randomized, controlled, assessor-blinded, two-arm trial initiated by investigators of the PROtective VEntilation NETwork. In total, 2378 patients will be randomly assigned to one of two different intraoperative mechanical ventilation strategies. Investigators screen patients aged 18 years or older, scheduled for open thoracic or video-assisted thoracoscopic surgery under general anesthesia requiring OLV, with a maximal body mass index of 35 kg/m 2 , and a planned duration of surgery of more than 60 min. Further, the expected duration of OLV shall be longer than two-lung ventilation, and lung separation is planned with a double lumen tube. Patients will be randomly assigned to PEEP of 10 cmH 2 O with lung RM, or PEEP of 5 cmH 2 O without RM. During two-lung ventilation tidal volume is set at 7 mL/kg predicted body weight and, during OLV, it will be decreased to 5 mL/kg. The occurrence of PPC will be recorded as a collapsed composite of single adverse pulmonary events and represents the primary endpoint. Discussion: PROTHOR is the first randomized controlled trial in patients undergoing thoracic surgery with OLV that is adequately powered to compare the effects of intraoperative high PEEP with RM versus low PEEP without RM on PPC. The results of the PROTHOR trial will support anesthesiologists in their decision to set intraoperative PEEP during protective ventilation for OLV in thoracic surgery. Trial registration: The trial was registered in clinicaltrials.gov (NCT02963025) on 15 November 2016.en_US
dc.identifier.citationTrials. Vol.20, No.1 (2019)en_US
dc.identifier.doi10.1186/s13063-019-3208-8en_US
dc.identifier.issn17456215en_US
dc.identifier.other2-s2.0-85064218287en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/51724
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064218287&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleProtective ventilation with high versus low positive end-expiratory pressure during one-lung ventilation for thoracic surgery (PROTHOR): Study protocol for a randomized controlled trialen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064218287&origin=inwarden_US

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