Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20865
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dc.contributor.authorScherer, Daniel J-
dc.contributor.authorNelson, Adam J-
dc.contributor.authorO'Brien, Richard C-
dc.contributor.authorKostner, Karam M-
dc.contributor.authorHare, David L-
dc.contributor.authorColquhoun, David M-
dc.contributor.authorBarter, Philip J-
dc.contributor.authorAylward, Philip-
dc.contributor.authorNicholls, Stephen J-
dc.contributor.authorWatts, Gerald F-
dc.date2019-05-08-
dc.date.accessioned2019-06-05T01:28:43Z-
dc.date.available2019-06-05T01:28:43Z-
dc.date.issued2019-10-
dc.identifier.citationHeart, Lung & Circulation 2019; 28(10): 1571-1579en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20865-
dc.description.abstractProprotein convertase subtilisin/kexin type 9 (PCSK9) monoclonal antibodies (mAb) have progressed from showing marked low density lipoprotein cholesterol lowering in early phase trials through to reducing cardiovascular events in large clinical outcome trials. Recently in Australia, the indication for evolocumab has been expanded to include both heterozygous and homozygous familial hypercholesterolaemia under the Pharmaceutical Benefits Scheme (PBS). With prices remaining high currently their use in non-familial hypercholesterolaemia in Australia remains by private prescription only at this stage. This manuscript summarises the major outcomes trials of the PCSK9 mAbs and the secondary analyses that have assessed their benefits in high risk patient groups, and describes the consensus of authors on which patients would most likely benefit from PCSK9 mAb therapy.en_US
dc.language.isoeng-
dc.subjectAtherosclerosisen_US
dc.subjectCardiovascular risken_US
dc.subjectLipidsen_US
dc.subjectPCSK9 inhibitorsen_US
dc.titleStatus of PCSK9 Monoclonal Antibodies in Australia.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleHeart, Lung & Circulationen_US
dc.identifier.affiliationDepartment of Medicine, Monash University, Melbourne, Vic, Australiaen_US
dc.identifier.affiliationSchool of Medical Sciences, University of New South Wales, Sydney, NSW, Australiaen_US
dc.identifier.affiliationFlinders University and Medical Centre, Adelaide, SA, Australiaen_US
dc.identifier.affiliationDepartment of Cardiology, Mater Hospital, University of Queensland, Brisbane, Qld, Australiaen_US
dc.identifier.affiliationSchool of Medicine, Faculty of Medicine and Health Sciences, University of Western Australia, Perth, Australiaen_US
dc.identifier.affiliationLipid Disorders Clinic, Department of Cardiology, Royal Perth Hospital, Perth, Australiaen_US
dc.identifier.affiliationSchool of Medicine, University of Queensland, Brisbane, Qld, Australiaen_US
dc.identifier.affiliationWesley Medical Centre, Wesley Hospital and Greenslopes Private Hospital, Brisbane, Qld, Australiaen_US
dc.identifier.affiliationFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Vic, Australiaen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.affiliationUniversity of Melbourne Clinical Schoolen_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationSouth Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australiaen_US
dc.identifier.affiliationUniversity of Adelaide, Adelaide, SA, Australiaen_US
dc.identifier.doi10.1016/j.hlc.2019.04.014en_US
dc.type.contentTexten_US
dc.identifier.pubmedid31104887-
dc.type.austinJournal Article-
dc.type.austinReview-
local.name.researcherHare, David L
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptEndocrinology-
crisitem.author.deptUniversity of Melbourne Clinical School-
crisitem.author.deptCardiology-
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