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Inhaled nebulised unfractionated heparin for the treatment of hospitalised patients with COVID-19: A multicentre case series of 98 patients

dc.contributor.authorVan Haren, Frank
dc.contributor.authorvan Loon, Lex
dc.contributor.authorSteins, Anne
dc.contributor.authorSmoot, Thomas L
dc.contributor.authorSas, Caitlin
dc.contributor.authorStaas, Sabrina
dc.contributor.authorVilaseca, Alicia B
dc.contributor.authorBarbera, Ruben A
dc.contributor.authorVidma, Gustavo
dc.contributor.authorBeccari, Hugo
dc.contributor.authorPopilevsky, Frida
dc.contributor.authorDaribayeva, Eleonora
dc.contributor.authorVenkatesan, Bhuvaneshwari
dc.contributor.authorMozes, Suzanne
dc.contributor.authorPostel, Rachel
dc.contributor.authorPopilevski, Natalie
dc.contributor.authorWebb, Andrew
dc.contributor.authorNunes, Quentin
dc.contributor.authorLaffey, John
dc.contributor.authorArtigas, Antonio
dc.contributor.authorSmith, Roger
dc.contributor.authorDixon, Barry
dc.contributor.authorRichardson, Alice
dc.contributor.authorYoon, Hwan-Jin
dc.contributor.authorPage, Clive
dc.date.accessioned2024-04-22T00:23:19Z
dc.date.issued2022
dc.date.updated2022-12-25T07:16:12Z
dc.description.abstractAims: To determine the safety and efficacy-potential of inhaled nebulised unfractionated heparin (UFH) in the treatment of hospitalised patients with COVID-19. Methods: Retrospective, uncontrolled multicentre single-arm case series of hospitalised patients with laboratory-confirmed COVID-19, treated with inhaled nebulised UFH (5000 IU q8h, 10 000 IU q4h, or 25 000 IU q6h) for 6 ± 3 (mean ± standard deviation) days. Outcomes were activated partial thromboplastin time (APTT) before treatment (baseline) and highest-level during treatment (peak), and adverse events including bleeding. Exploratory efficacy outcomes were oxygenation, assessed by ratio of oxygen saturation to fraction of inspired oxygen (FiO2) and FiO2, and the World Health Organisation modified ordinal clinical scale. Results: There were 98 patients included. In patients on stable prophylactic or therapeutic systemic anticoagulant therapy but not receiving therapeutic UFH infusion, APTT levels increased from baseline of 34 ± 10 seconds to a peak of 38 ± 11 seconds (P <.0001). In 3 patients on therapeutic UFH infusion, APTT levels did not significantly increase from baseline of 72 ± 20 to a peak of 84 ± 28 seconds (P =.17). Two patients had serious adverse events: bleeding gastric ulcer requiring transfusion and thigh haematoma; both were on therapeutic anticoagulation. Minor bleeding occurred in 16 patients, 13 of whom were on therapeutic anticoagulation. The oxygen saturation/FiO2 ratio and the FiO2 worsened before and improved after commencement of inhaled UFH (change in slope, P <.001). Conclusion: Inhaled nebulised UFH in hospitalised patients with COVID-19 was safe. Although statistically significant, inhaled nebulised UFH did not produce a clinically relevant increase in APTT (peak values in the normal range). Urgent randomised evaluation of nebulised UFH in patients with COVID-19 is warranted and several studies are currently underway.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0306-5251en_AU
dc.identifier.urihttp://hdl.handle.net/1885/316938
dc.language.isoen_AUen_AU
dc.publisherWiley-Blackwellen_AU
dc.rights© 2022 British Pharmacological Societyen_AU
dc.sourceBritish Journal of Clinical Pharmacologyen_AU
dc.subjectcase seriesen_AU
dc.subjectCOVID-19en_AU
dc.subjectinhaled heparinen_AU
dc.subjectnebulised heparinen_AU
dc.subjectpandemicen_AU
dc.subjectrespiratory failureen_AU
dc.subjectSARS-CoV-2en_AU
dc.subjectunfractionated heparinen_AU
dc.titleInhaled nebulised unfractionated heparin for the treatment of hospitalised patients with COVID-19: A multicentre case series of 98 patientsen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue6en_AU
local.bibliographicCitation.lastpage2813en_AU
local.bibliographicCitation.startpage2802en_AU
local.contributor.affiliationvan Haren, Frank, College of Health and Medicine, ANUen_AU
local.contributor.affiliationvan Loon, Lex Maxim, College of Health and Medicine, ANUen_AU
local.contributor.affiliationSteins, Anne, College of Health and Medicine, ANUen_AU
local.contributor.affiliationSmoot, Thomas L, Frederick Memorial Hospitalen_AU
local.contributor.affiliationSas, Caitlin, Frederick Memorial Hospitalen_AU
local.contributor.affiliationStaas, Sabrina, Frederick Memorial Hospitalen_AU
local.contributor.affiliationVilaseca, Alicia B, Service of Haematology and Haemostasis, San Camilo Clinicen_AU
local.contributor.affiliationBarbera, Ruben A, 8 Service of Haematology and Haemostasis, San Camilo Clinic, Buenos Aires, Argentinaen_AU
local.contributor.affiliationVidma, Gustavo, Service of Haematology and Haemostasis, San Camilo Clinicen_AU
local.contributor.affiliationBeccari, Hugo, Service of Haematology and Haemostasis, San Camilo Clinicen_AU
local.contributor.affiliationPopilevsky, Frida, Surgical Intensive Care Unit, Coney Island Hospital, Brooklynen_AU
local.contributor.affiliationDaribayeva, Eleonora, Surgical Intensive Care Unit, Coney Island Hospital, Brooklynen_AU
local.contributor.affiliationVenkatesan, Bhuvaneshwari, Surgical Intensive Care Unit, Coney Island Hospital, Brooklynen_AU
local.contributor.affiliationMozes, Suzanne, Surgical Intensive Care Unit, Coney Island Hospital, Brooklynen_AU
local.contributor.affiliationPostel, Rachel, Surgical Intensive Care Unit, Coney Island Hospital, Brooklynen_AU
local.contributor.affiliationPopilevski, Natalie, Surgical Intensive Care Unit, Coney Island Hospital, Brooklynen_AU
local.contributor.affiliationWebb, Andrew, Clinical Pharmacology, School of Cardiovascular Medicine & Sciences, King’s Collegeen_AU
local.contributor.affiliationNunes, Quentin, University of Liverpoolen_AU
local.contributor.affiliationLaffey, John, National University of Ireland Galwayen_AU
local.contributor.affiliationArtigas, Antonio, Autonomous University of Barcelonaen_AU
local.contributor.affiliationSmith, Roger, St Vincent's Hospitalen_AU
local.contributor.affiliationDixon, Barry, St Vincent's Hospitalen_AU
local.contributor.affiliationRichardson, Alice, RSCH Research & Innovation Portfolio, ANUen_AU
local.contributor.affiliationYoon, Hwan-Jin, RSCH Research & Innovation Portfolio, ANUen_AU
local.contributor.affiliationPage, Clive, King's College Londonen_AU
local.contributor.authoruidvan Haren, Frank, u5325459en_AU
local.contributor.authoruidvan Loon, Lex Maxim, u1099389en_AU
local.contributor.authoruidSteins, Anne, u1099391en_AU
local.contributor.authoruidRichardson, Alice, u3767151en_AU
local.contributor.authoruidYoon, Hwan-Jin, u3128131en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor320103 - Respiratory diseasesen_AU
local.identifier.absfor320212 - Intensive careen_AU
local.identifier.absseo200311 - Urgent and critical care, and emergency medicineen_AU
local.identifier.ariespublicationa383154xPUB26371en_AU
local.identifier.citationvolume88en_AU
local.identifier.doi10.1111/bcp.15212en_AU
local.identifier.scopusID2-s2.0-85122888935
local.publisher.urlhttps://www.wiley.com/en-gben_AU
local.type.statusPublished Versionen_AU

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