Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30506
Full metadata record
DC FieldValueLanguage
dc.contributor.authorProsser, Hamish C-
dc.contributor.authorPeck, Kah Yong-
dc.contributor.authorDinh, Diem-
dc.contributor.authorRoberts, Louise-
dc.contributor.authorChandrasekhar, Jaya-
dc.contributor.authorBrennan, Angela-
dc.contributor.authorDuffy, Stephen J-
dc.contributor.authorClark, David J-
dc.contributor.authorAjani, Andrew E-
dc.contributor.authorOqueli, Ernesto-
dc.contributor.authorSebastian, Martin-
dc.contributor.authorReid, Christopher M-
dc.contributor.authorFreeman, Melanie-
dc.contributor.authorSajeev, Jithin K-
dc.contributor.authorTeh, Andrew W-
dc.date2022-
dc.date.accessioned2022-07-06T06:23:48Z-
dc.date.available2022-07-06T06:23:48Z-
dc.date.issued2022-07-
dc.identifier.citationClinical Research in Cardiology 2022; 111(7):776-786.en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30506-
dc.description.abstractThe use of angiotensin-converting enzyme inhibitors (ACEi) or angiotensin II-receptor blockers (ARBs) post-myocardial infarction (MI) is supported by evidence based on trials performed in the thrombolysis era. This was prior to primary percutaneous coronary intervention (PCI) being routine practice, and with little direct evidence for the use of these medications in patients with preserved left ventricular (LV) function. This study sought to determine whether there is an association between ACEi/ARB use after PCI for acute coronary syndrome (ACS) and long-term all-cause mortality, with a particular focus on patients with preserved LV function. This multicentre, observational study evaluated prospectively collected data of 21,388 patients (> 18 years old) that underwent PCI for NSTEMI and STEMI between 2005 and 2018, and were alive at 30 day follow-up. In total, 83.8% of patients were using ACEi/ARBs. Kaplan-Meier analysis demonstrated ACEi/ARB use was associated with a significantly lower mortality in the entire cohort (15.0 vs. 22.7%; p < 0.001) with a mean follow-up of 5.58 years; and independently associated with 24% lower mortality by Cox proportional hazards modelling (HR 0.76, CI 0.67-0.85, p < 0.001). ACEi/ARB therapy was also associated with significantly lower mortality in patients with reduced or preserved LV function, with greater survival benefit with worse LV dysfunction. ACEi/ARB therapy post-PCI is associated with significantly lower long-term mortality in patients with reduced and preserved LV function. These findings provide contemporary evidence for using these agents in the current era of routine primary PCI, including those with preserved EF.en
dc.language.isoeng-
dc.subjectAngiotensin converting enzyme inhibitorsen
dc.subjectAngiotensin receptor blockersen
dc.subjectHeart failureen
dc.subjectPercutaneous coronary interventionen
dc.subjectSTEMI/NSTEMIen
dc.titleRole of renin-angiotensin system antagonists on long-term mortality post-percutaneous coronary intervention in reduced and preserved ejection fraction.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical research in cardiology : official journal of the German Cardiac Societyen
dc.identifier.affiliationDepartment of Cardiology, Eastern Health, Box Hill Hospital, Level 2, 8 Arnold Street, Box Hill, VIC, 3128, Australia..en
dc.identifier.affiliationEastern Health Clinical School, Monash University, Melbourne, VIC, Australia..en
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia..en
dc.identifier.affiliationEastern Health Clinical School, Monash University, Melbourne, VIC, Australia..en
dc.identifier.affiliationSchool of Medicine, Deakin University, Geelong, Australia..en
dc.identifier.affiliationDepartment of Cardiology, Alfred Health, The Alfred Hospital, Melbourne, VIC, Australia..en
dc.identifier.affiliationCardiologyen
dc.identifier.affiliationDepartment of Cardiology, Royal Melbourne Hospital, Parkville, VIC, Australia..en
dc.identifier.affiliationDepartment of Cardiology, Ballarat Health Services, Ballarat, VIC, Australia..en
dc.identifier.affiliationDepartment of Cardiology, Barwon Health, University Hospital, Geelong, VIC, Australia..en
dc.identifier.affiliationSchool of Public Health, Curtin University, Perth, WA, Australia..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35050405/en
dc.identifier.doi10.1007/s00392-021-01985-xen
dc.type.contentTexten
dc.identifier.orcid0000-0003-4074-3610en
dc.identifier.pubmedid35050405-
local.name.researcherClark, David J
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptCardiology-
crisitem.author.deptUniversity of Melbourne Clinical School-
crisitem.author.deptCardiology-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

74
checked on Dec 20, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.