Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32088
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dc.contributor.authorWard, Natalie C-
dc.contributor.authorWatts, Gerald F-
dc.contributor.authorBishop, Warrick-
dc.contributor.authorColquhoun, David-
dc.contributor.authorHamilton-Craig, Christian-
dc.contributor.authorHare, David L-
dc.contributor.authorKangaharan, Nadarajah-
dc.contributor.authorKostner, Karam M-
dc.contributor.authorKritharides, Leonard-
dc.contributor.authorO'Brien, Richard C-
dc.contributor.authorMori, Trevor A-
dc.contributor.authorNestel, Paul J-
dc.contributor.authorNicholls, Stephen J-
dc.contributor.authorPsaltis, Peter J-
dc.contributor.authorRaffoul, Natalie-
dc.contributor.authorWhite, Harvey D-
dc.contributor.authorSullivan, David R-
dc.date2023-
dc.date.accessioned2023-02-07T05:52:01Z-
dc.date.available2023-02-07T05:52:01Z-
dc.date.issued2023-01-25-
dc.identifier.citationHeart, lung & circulation 2023-03; 32(3)-
dc.identifier.issn1444-2892-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32088-
dc.description.abstractThis position statement provides guidance to cardiologists and related specialists on the management of adult patients with elevated lipoprotein(a) [Lp(a)]. Elevated Lp(a) is an independent and causal risk factor for atherosclerotic cardiovascular disease (ASCVD) and calcific aortic valve disease (CAVD). While circulating Lp(a) levels are largely determined by ancestry, they are also influenced by ethnicity, hormones, renal function, and acute inflammatory events, such that measurement should be done after accounting for these factors. Further, circulating Lp(a) concentrations should be estimated using an apo(a)-isoform independent assay that employs appropriate calibrators and reports the results in molar units (nmol/L). Selective screening strategies of high-risk patients are recommended, but universal screening of the population is currently not advised. Testing for elevated Lp(a) is recommended in all patients with premature ASCVD and those considered to be at intermediate-to-high risk of ASCVD. Elevated Lp(a) should be employed to assess and stratify risk and to enable a decision on initiation or intensification of preventative treatments, such as cholesterol lowering therapy. In adult patients with elevated Lp(a) at intermediate-to-high risk of ASCVD, absolute risk should be reduced by addressing all modifiable behavioural, lifestyle, psychosocial and clinical risk factors, including maximising cholesterol-lowering with statin and ezetimibe and, where appropriate, PCSK9 inhibitors. Apheresis should be considered in patients with progressive ASCVD. New ribonucleic acid (RNA)-based therapies which directly lower Lp(a) are undergoing clinical trials.-
dc.language.isoeng-
dc.subjectAtherosclerotic cardiovascular disease-
dc.subjectAustralian Atherosclerosis Society-
dc.subjectCardiovascular risk-
dc.subjectLipoprotein(a)-
dc.titleAustralian Atherosclerosis Society Position Statement on Lipoprotein(a): Clinical and Implementation Recommendations.-
dc.typeJournal Article-
dc.identifier.journaltitleHeart, lung & circulation-
dc.identifier.affiliationLipid Disorders Clinic, Department of Cardiology, Royal Perth Hospital, Perth, WA, Australia.-
dc.identifier.affiliationDobney Hypertension Centre, Medical School, University of Western Australia, Perth, WA, Australia.-
dc.identifier.affiliationFaculty of Medicine, Wesley Medical Centre, Brisbane, Qld, Australia-
dc.identifier.affiliationFaculty of Medicine, Medical School, University of Queensland, Brisbane, Qld, Australia.-
dc.identifier.affiliationFaculty of Medicine, University of Queensland, Brisbane, Qld, Australia-
dc.identifier.affiliationFaculty of Medicine, Dentistry and Health, School of Medicine, Griffith University, Sunshine Coast, Qld, Australia.-
dc.identifier.affiliationDepartment of Cardiology, Mater Hospital, Brisbane, Qld, Australia-
dc.identifier.affiliationMedical School, University of Queensland, Brisbane, Qld, Australia.-
dc.identifier.affiliationAdelaide Medical School, University of Adelaide, Adelaide, SA, Australia-
dc.identifier.affiliationVascular Research Centre, Lifelong Health Theme, South Australian Health & Medical Research Institute, Adelaide, SA, Australia-
dc.identifier.affiliationDepartment of Cardiology, Central Adelaide Local Health Network, Adelaide, SA, Australia.-
dc.identifier.affiliationMedical School, University of Sydney, Sydney, NSW, Australia-
dc.identifier.affiliationCharles Perkins Centre, University of Sydney, Sydney, NSW, Australia, and Department of Biochemistry, Royal Prince Alfred Hospital, Sydney, NSW, Australia.-
dc.identifier.affiliationMedical School, University of Western Australia, Perth, WA, Australia-
dc.identifier.affiliationPrivate Practice, Tas, Australia.-
dc.identifier.affiliationFaculty of Medicine, Dentistry & Health Sciences, University of Melbourne, Melbourne, Vic, Australia and Department of Cardiology, Austin Hospital, Heidelberg, Vic, Australia.-
dc.identifier.affiliationDepartment of Cardiology, Royal Darwin Hospital, Darwin, NT, Australia.-
dc.identifier.affiliationSydney Medical School, Faculty of Medicine, University of Sydney, Sydney, NSW, Australia and Department of Cardiology, Concord Repatriation General Hospital, Sydney Local Health District, Sydney, NSW, Australia.-
dc.identifier.affiliationMedical School, University of Western Australia, Perth, WA, Australia.-
dc.identifier.affiliationBaker Heart & Diabetes Institute, Melbourne, Vic, Australia.-
dc.identifier.affiliationMonash Cardiovascular Research Centre, Victorian Heart Institute, Monash University, Melbourne, Vic, Australia.-
dc.identifier.affiliationNational Heart Foundation, Sydney, NSW, Australia.-
dc.identifier.affiliationTe Whatu Ora-Health New Zealand, Green Lane Cardiovascular Service, Te Toka Tumai, Auckland, New Zealand.-
dc.identifier.affiliationMedicine (University of Melbourne)-
dc.identifier.affiliationCardiology-
dc.identifier.doi10.1016/j.hlc.2022.11.015-
dc.type.contentText-
dc.identifier.pubmedid36707360-
dc.description.volume32-
dc.description.issue3-
dc.description.startpage287-
dc.description.endpage296-
dc.subject.meshtermssecondaryAtherosclerosis/diagnosis-
dc.subject.meshtermssecondaryAtherosclerosis/prevention & control-
dc.subject.meshtermssecondaryAustralia/epidemiology-
dc.subject.meshtermssecondaryCardiovascular Diseases/complications-
local.name.researcherHare, David L
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptCardiology-
crisitem.author.deptEndocrinology-
crisitem.author.deptUniversity of Melbourne Clinical School-
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