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Can nebulised HepArin Reduce morTality and time to Extubation in patients with COVID-19 Requiring invasive ventilation Meta-Trial (CHARTER-MT): Protocol and statistical analysis plan for an investigator-initiated international meta-trial of prospective randomised clinical studies

dc.contributor.authorVan Haren, Frank
dc.contributor.authorLaffey, John G
dc.contributor.authorArtigas, Antonio
dc.contributor.authorPage, Clive
dc.contributor.authorSchultz, Marcus J
dc.contributor.authorCosgrave, David
dc.contributor.authorMcNicholas, Bairbre
dc.contributor.authorSmoot, Thomas L
dc.contributor.authorNunes, Quentin
dc.contributor.authorRichardson, Alice
dc.contributor.authorYoon, Hwan-Jin
dc.contributor.authorvan Loon, Lex M
dc.contributor.authorGhosh, Angajendra
dc.contributor.authorSaid, Simone
dc.contributor.authorPanwar, Rakshit
dc.contributor.authorSmith, Roger
dc.contributor.authorSantamaria, John D
dc.contributor.authorDixon, Barry
dc.date.accessioned2022-12-08T03:29:21Z
dc.date.available2022-12-08T03:29:21Z
dc.date.issued2022-02-01
dc.description.abstractThere is significant interest in the potential for nebulised unfractionated heparin (UFH), as a novel therapy for patients with COVID-19 induced acute hypoxaemic respiratory failure requiring invasive ventilation. The scientific and biological rationale for nebulised heparin stems from the evidence for extensive activation of coagulation resulting in pulmonary microvascular thrombosis in COVID-19 pneumonia. Nebulised delivery of heparin to the lung may limit alveolar fibrin deposition and thereby limit progression of lung injury. Importantly, laboratory studies show that heparin can directly inactivate the SARS-CoV-2 virus, thereby prevent its entry into and infection of mammalian cells. UFH has additional anti-inflammatory and mucolytic properties that may be useful in this context. METHODS AND INTERVENTION: The Can nebulised HepArin Reduce morTality and time to Extubation in Patients with COVID-19 Requiring invasive ventilation Meta-Trial (CHARTER-MT) is a collaborative prospective individual patient data analysis of on-going randomised controlled clinical trials across several countries in five continents, examining the effects of inhaled heparin in patients with COVID-19 requiring invasive ventilation on various endpoints. Each constituent study will randomise patients with COVID-19 induced respiratory failure requiring invasive ventilation. Patients are randomised to receive nebulised heparin or standard care (open label studies) or placebo (blinded placebo-controlled studies) while under invasive ventilation. Each participating study collect a pre-defined minimum dataset. The primary outcome for the meta-trial is the number of ventilator-free days up to day 28 day, defined as days alive and free from invasive ventilation.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0306-5251en_AU
dc.identifier.urihttp://hdl.handle.net/1885/281653
dc.language.isoen_AUen_AU
dc.provenanceThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.en_AU
dc.publisherBritish Pharmacological Societyen_AU
dc.rights© 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Societyen_AU
dc.rights.licenseCreative Commons Attribution-NonCommercial Licenseen_AU
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_AU
dc.sourceBritish journal of clinical pharmacologyen_AU
dc.subjectardsen_AU
dc.subjectcovid-19en_AU
dc.subjectrcten_AU
dc.subjectsarsen_AU
dc.subjectsars-cov-2en_AU
dc.subjectmeta-trialen_AU
dc.subjectnebulised heparinen_AU
dc.subjectpandemicen_AU
dc.subjectrandomised studyen_AU
dc.subjectrespiratory failureen_AU
dc.subjectunfractionated heparinen_AU
dc.subjectairway extubationen_AU
dc.subjectheparinen_AU
dc.subjecthumansen_AU
dc.subjectlungen_AU
dc.subjectrandomized controlled trials as topicen_AU
dc.subjectsars-cov-2en_AU
dc.subjecttreatment outcomeen_AU
dc.subjectcovid-19en_AU
dc.subjectnoninvasive ventilationen_AU
dc.subjectrespiratory insufficiencyen_AU
dc.titleCan nebulised HepArin Reduce morTality and time to Extubation in patients with COVID-19 Requiring invasive ventilation Meta-Trial (CHARTER-MT): Protocol and statistical analysis plan for an investigator-initiated international meta-trial of prospective randomised clinical studiesen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue7en_AU
local.bibliographicCitation.lastpage3287en_AU
local.bibliographicCitation.startpage3272en_AU
local.contributor.affiliationvan Haren, F., The Australian National Universityen_AU
local.contributor.affiliationRichardson, A., The Australian National Universityen_AU
local.contributor.affiliationYoon, Hwan-Jin, The Australian National Universityen_AU
local.contributor.affiliationvan Loon, Lex, The Australian National Universityen_AU
local.contributor.authoruidu3767151en_AU
local.identifier.ariespublicationa383154xPUB26482
local.identifier.citationvolume88en_AU
local.identifier.doi10.1111/bcp.15253en_AU
local.identifier.essn1365-2125en_AU
local.publisher.urlhttps://www.wiley.com/en-gben_AU
local.type.statusPublished Versionen_AU

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