Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/40687
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dc.contributor.authorFord S.en
dc.contributor.authorBurke J.en
dc.contributor.authorKausman J.en
dc.contributor.authorHewitt I.en
dc.contributor.authorParnham A.en
dc.contributor.authorIsbel N.en
dc.contributor.authorMallett A.en
dc.contributor.authorHughes P.en
dc.contributor.authorSzer J.en
dc.contributor.authorTuckfield A.en
dc.contributor.authorVan Eps C.en
dc.contributor.authorCambell S.B.en
dc.contributor.authorHawley C.en
dc.date.accessioned2021-05-14T13:55:14Zen
dc.date.available2021-05-14T13:55:14Zen
dc.date.copyright2015en
dc.date.created20151007en
dc.date.issued2015-10-07en
dc.identifier.citationInternal Medicine Journal. 45 (10) (pp 1054-1065), 2015. Date of Publication: 01 Oct 2015.en
dc.identifier.issn1444-0903en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/40687en
dc.description.abstractBackground/Aim: This study aimed to report the clinical characteristics and outcomes of Australian patients treated with eculizumab for atypical haemolytic uraemic syndrome (aHUS). Method(s): A retrospective cohort study was undertaken of all patients in Australia treated with eculizumab provided in a compassionate access programme for a clinical diagnosis of aHUS using prospectively collected clinical data. Result(s): A total of 10 patients with a median age of 23.5 years (interquartile range (IQR) 24.83 years) received compassionate access eculizumab for aHUS in Australia. Eight patients were female, and three had a family history of aHUS. Three received eculizumab for an initial acute aHUS presentation, three for relapsing and refractory acute aHUS, two for de novo aHUS post-renal transplantation, and one each for aHUS recurrence post-transplantation and facilitation of transplantation with a history of aHUS. The median duration of eculizumab therapy has been 911.5 days (IQR 569 days) with a cumulative exposure of 9184 days. At baseline all patients had renal and extra-renal aHUS involvement, with up to three non-renal organs affected. All but one patient, who died from uncontrollable gastrointestinal aHUS manifestations, have continued. The nine continuing patients achieved remission of aHUS. Two of the four patients requiring renal replacement therapy (RRT) at eculizumab commencement subsequently ceased RRT. Clinical events occurring in this cohort while on eculizumab treatment included neutropenia (two), posterior reversible encephalopathy syndrome (one), cardiomyopathy (one), pulmonary embolus (one), antibody-mediated rejection resulting in renal graft failure (one), iron deficiency (one), gastrointestinal haemorrhage (one) and death (one). Conclusion(s): Eculizumab has been an effective therapy for aHUS in this cohort, including when other therapies have failed.Copyright © 2015 Royal Australasian College of Physicians.en
dc.languageenen
dc.languageEnglishen
dc.publisherBlackwell Publishing (E-mail: info@asia.blackpublishing.com.au)en
dc.relation.ispartofInternal Medicine Journalen
dc.titleAtypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: The experience of the Australian compassionate access cohort.en
dc.typeArticleen
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/imj.12864en
dc.publisher.placeAustraliaen
dc.identifier.pubmedid26247170 [http://www.ncbi.nlm.nih.gov/pubmed/?term=26247170]en
dc.identifier.source606257398en
dc.identifier.institution(Mallett) Department of Renal Medicine, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia (Mallett, Van Eps, Cambell, Hawley, Burke, Isbel) Centre for Kidney Disease Research, Centre for Chronic Disease, CKD.QLD, School of Medicine, University of Queensland, Brisbane, QLD, Australia (Van Eps, Cambell, Hawley, Burke, Isbel) Department of Nephrology, Princess Alexandra Hospital, Brisbane, QLD, Australia (Parnham) Department of Nephrology, Gold Coast Hospital, Gold Coast, QLD, Australia (Hughes) Department of Nephrology, Royal Melbourne Hospital, Melbourne, VIC, Australia (Szer, Tuckfield) Department of Clinical Haematology and BMT Service, Royal Melbourne Hospital, Melbourne, VIC, Australia (Kausman) Department of Nephrology, The Royal Children's Hospital Melbourne, Melbourne, VIC, Australia (Ford) Department of Nephrology, Monash Medical Centre, Melbourne, VIC, Australia (Hewitt) Department of Nephrology, Princess Margaret Hospital for Children, Perth, WA, Australiaen
dc.description.addressA. Mallett, Department of Renal Medicine, Royal Brisbane and Women's Hospital, Level 9, Ned Hanlon Building, Butterfield Street, Herston, Brisbane, QLD 4029, Australia. E-mail: andrew.mallett@health.qld.gov.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2016 Elsevier B.V., All rights reserved.en
dc.subect.keywordsAtypical haemolytic uraemic syndrome Eculizumab Thrombotic microangiopathy Transplantationen
dc.identifier.authoremailMallett A.; andrew.mallett@health.qld.gov.auen
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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