Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/28864
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dc.contributor.authorKeat K.en
dc.contributor.authorOjaimi S.en
dc.contributor.authorTran T.en
dc.contributor.authorWest T.A.en
dc.contributor.authorMalik S.en
dc.contributor.authorNalpantidis A.en
dc.contributor.authorCannon C.en
dc.contributor.authorBhonagiri D.en
dc.contributor.authorChan K.en
dc.contributor.authorCheong E.en
dc.contributor.authorWan Sai Cheong J.en
dc.contributor.authorCheung W.en
dc.contributor.authorChoudhury F.en
dc.contributor.authorErnest D.en
dc.contributor.authorFarah C.S.en
dc.contributor.authorFernando S.en
dc.contributor.authorKanapathipillai R.en
dc.contributor.authorKol M.en
dc.contributor.authorMurfin B.en
dc.contributor.authorNaqvi H.en
dc.contributor.authorShah A.en
dc.contributor.authorWagh A.en
dc.contributor.authorFrankum B.en
dc.contributor.authorRiminton S.en
dc.date.accessioned2021-05-14T09:43:33Zen
dc.date.available2021-05-14T09:43:33Zen
dc.date.copyright2020en
dc.date.created20200824en
dc.date.issued2020-08-24en
dc.identifier.citationInternational Journal of Rheumatic Diseases. 23 (8) (pp 1030-1039), 2020. Date of Publication: 01 Aug 2020.en
dc.identifier.issn1756-1841en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/28864en
dc.description.abstractAim: To describe the first Australian cases of severe acute respiratory syndrome-coronavirus 2 (SARS-CoV2) disease (COVID-19) pneumonia treated with the interleukin-6 receptor antagonist tocilizumab. Method(s): Retrospective, open-label, real-world, uncontrolled, single-arm case series conducted in 2 tertiary hospitals in NSW, Australia and 1 tertiary hospital in Victoria, Australia. Five adult male patients aged between 46 and 74 years with type 1 respiratory failure due to COVID-19 pneumonia requiring intensive care unit (ICU) admission and biochemical evidence of systemic hyperinflammation (C-reactive protein greater than 100 mg/L; ferritin greater than 700 mug/L) were administered variable-dose tocilizumab. Result(s): At between 13 and 26 days follow-up, all patients are alive and have been discharged from ICU. Two patients have been discharged home. Two patients avoided endotracheal intubation. Oxygen therapy has been ceased in three patients. Four adverse events potentially associated with tocilizumab therapy occurred in three patients: ventilator-associated pneumonia, bacteremia associated with central venous catheterization, myositis and hepatitis. All patients received broad-spectrum antibiotics, 4 received corticosteroids and 2 received both lopinavir/ritonavir and hydroxychloroquine. The time from first tocilizumab administration to improvement in ventilation, defined as a 25% reduction in fraction of inspired oxygen required to maintain peripheral oxygen saturation greater than 92%, ranged from 7 hours to 4.6 days. Conclusion(s): Tocilizumab use was associated with favorable clinical outcome in our patients. We recommend tocilizumab be included in randomized controlled trials of treatment for patients with severe COVID-19 pneumonia, and be considered for compassionate use in such patients pending the results of these trials.Copyright © 2020 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltden
dc.languageEnglishen
dc.languageenen
dc.publisherBlackwell Publishingen
dc.relation.ispartofInternational Journal of Rheumatic Diseasesen
dc.subject.meshsingle drug dose-
dc.subject.meshstaphylococcal bacteremia-
dc.subject.meshventilator associated pneumonia-
dc.subject.meshVictoria-
dc.subject.meshvirus pneumonia-
dc.subject.meshazithromycin-
dc.subject.meshC reactive protein-
dc.subject.meshceftriaxone-
dc.subject.meshferritin-
dc.subject.meshhydroxychloroquine [Adverse Drug Reaction]-
dc.subject.meshhydroxychloroquine-
dc.subject.meshlopinavir plus ritonavir [Adverse Drug Reaction]-
dc.subject.meshlopinavir plus ritonavir-
dc.subject.meshmethylprednisolone-
dc.subject.meshnoradrenalin-
dc.subject.meshpiperacillin plus tazobactam-
dc.subject.meshprednisone-
dc.subject.meshprednisone [Oral Drug Administration]-
dc.subject.meshtocilizumab [Adverse Drug Reaction]-
dc.subject.meshvancomycin-
dc.subject.meshfraction of inspired oxygen-
dc.subject.meshtocilizumab-
dc.subject.meshacute kidney failure-
dc.subject.meshaged-
dc.subject.meshartificial ventilation-
dc.subject.meshAustralian-
dc.subject.meshcatheter removal-
dc.subject.meshcoronavirus disease 2019-
dc.subject.meshcytokine release syndrome-
dc.subject.meshdelirium-
dc.subject.meshdrug withdrawal-
dc.subject.meshendotracheal intubation-
dc.subject.mesheosinophilia-
dc.subject.meshextubation-
dc.subject.meshfatty liver-
dc.subject.meshfever-
dc.subject.meshhepatitis-
dc.subject.meshhypoxia-
dc.subject.meshintensive care-
dc.subject.meshkidney failure-
dc.subject.meshmyositis-
dc.subject.meshNew South Wales-
dc.subject.meshoxygen saturation-
dc.subject.meshoxygen therapy-
dc.subject.meshprone position-
dc.subject.meshQT prolongation-
dc.subject.meshrespiratory failure-
dc.subject.meshrespiratory tract parameters-
dc.subject.meshsedation-
dc.titleTocilizumab for severe COVID-19 pneumonia: Case series of 5 Australian patients.en
dc.typeArticleen
dc.identifier.affiliationHaematology-
dc.identifier.affiliationIntensive Care-
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/1756-185X.13913-
dc.publisher.placeAustraliaen
dc.identifier.pubmedid32881350 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32881350]en
dc.identifier.source2005850619en
dc.identifier.institution(West, Frankum, Keat) Department of Immunology and Allergy, Campbelltown Hospital, Sydney, NSW, Australia (Malik, Farah, Riminton) Department of Respiratory Medicine, Concord Hospital, Sydney, NSW, Australia (Nalpantidis) Clinical Haematology Unit, Monash Health, Melbourne, VIC, Australia (Tran) Department of Medicine, Campbelltown Hospital, Sydney, NSW, Australia (Cannon) Department of Medicine, Concord Hospital, Sydney, NSW, Australia (Bhonagiri) Intensive Care Unit, Campbelltown Hospital, Sydney, NSW, Australia (Chan, Choudhury, Naqvi) Department of Respiratory Medicine, Campbelltown Hospital, Sydney, NSW, Australia (Cheong, Fernando) Department of Microbiology and Infectious Diseases, Concord Hospital, Sydney, NSW, Australia (Wan Sai Cheong) School of Medicine, Western Sydney University, Sydney, NSW, Australia (Cheung, Kol, Shah, Wagh) Intensive Care Unit, Concord Hospital, Sydney, NSW, Australia (Ernest, Murfin) Intensive Care Unit, Monash Health, Melbourne, VIC, Australia (Kanapathipillai, Ojaimi) Monash Infectious Diseases, Monash University, Melbourne, VIC, Australiaen
dc.description.addressT.A. West, Department of Immunology and Allergy, Campbelltown Hospital, Sydney, NSW, Australia. E-mail: timothy.west@health.nsw.gov.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.subect.keywordsacute respiratory distress syndrome coronavirus immunomodulation interleukin-6 pneumonia tocilizumab viralen
dc.identifier.authoremailWest T.A.; timothy.west@health.nsw.gov.auen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptOrthopaedic Surgery-
crisitem.author.deptEmergency Medicine-
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