Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22444
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dc.contributor.authorYudi, Matias B-
dc.contributor.authorFarouque, Omar-
dc.contributor.authorAndrianopoulos, Nick-
dc.contributor.authorAjani, Andrew E-
dc.contributor.authorBrennan, Angela-
dc.contributor.authorMurphy, Alexandra C-
dc.contributor.authorLefkovits, Jeffrey-
dc.contributor.authorReid, Christopher M-
dc.contributor.authorOqueli, Ernesto-
dc.contributor.authorSebastian, Martin-
dc.contributor.authorDuffy, Stephen J-
dc.contributor.authorClark, David J-
dc.date2020-01-14-
dc.date.accessioned2020-01-20T05:24:55Z-
dc.date.available2020-01-20T05:24:55Z-
dc.date.issued2020-03-
dc.identifier.citationInternal Medicine Journal 2021; 51(3): 366-374en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22444-
dc.description.abstractOptimal secondary prevention pharmacotherapy is the cornerstone of post-acute coronary syndrome (ACS) management. The prognostic impact of not receiving five guideline-recommended therapies is poorly described. We aim to ascertain the prognostic significance of suboptimal pharmacotherapy in ACS survivors. Consecutive patients with ACS from the Melbourne Interventional Group registry who were alive at 30-days following their index percutaneous coronary intervention were included. Patients were divided into three categories based on the number of secondary prevention medications prescribed. The optimal medical therapy (OMT), near-optimal medical therapy (NMT), suboptimal medical therapy (SMT) groups were prescribed 5, 4 and ≤3 medications, respectively. Primary endpoint was long-term mortality. Cox-proportional hazard modelling was undertaken to assess independent predictors of survival. Of the 9,375 patients included, 5,678 (60.6%) received OMT, 2,903 (31.0%) received NMT and 794 (8.5%) received SMT. Patients receiving SMT were older, more likely to be female and had higher burden of co-morbidities (renal impairment, congestive heart failure, diabetes, peripheral vascular disease; p<0.01 for all). SMT was associated with higher long-term mortality at 3.9±2.2 years when compared to NMT and OMT (16.8% vs. 10.5% vs. 8.2%, p<0.001). Compared to OMT, SMT was an independent predictor of long-term mortality (HR 1.62, 95% CI 1.30-2.02, p<0.01) while NMT was associated with a clinically significant 14% mortality hazard (HR 1.14, 95% CI 0.97-1.34, p=0.11). There is a graded long-term hazard associated with not receiving OMT after an ACS. Improvements in secondary prevention pharmacotherapy models of care are warranted to further decrease long-term mortality. This article is protected by copyright. All rights reserved.en_US
dc.language.isoeng-
dc.subjectacute coronary syndromesen_US
dc.subjectpercutaneous coronary interventionen_US
dc.subjectsecondary preventionen_US
dc.subjectsurvivalen_US
dc.titlePrognostic Significance of Suboptimal Secondary Prevention Pharmacotherapy After Acute Coronary Syndromes.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInternal Medicine Journalen_US
dc.identifier.affiliationSchool of Public Health, Curtin University, Perth, Western Australiaen_US
dc.identifier.affiliationDepartment of Cardiology, Royal Melbourne Hospital, Melbourne, Australiaen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Cardiology, Ballarat Base Hospital, Ballarat, Australiaen_US
dc.identifier.affiliationCentre of Cardiovascular Research and Education in Therapeutics (CCRE), Monash University, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Cardiology, Alfred Health, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Cardiology, Barwon Health, Geelong, Australiaen_US
dc.identifier.doi10.1111/imj.14750en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-4248-7537en_US
dc.identifier.orcid0000-0002-4518-5948en_US
dc.identifier.orcid0000-0002-3706-4150en_US
dc.identifier.pubmedid31943665-
dc.type.austinJournal Article-
local.name.researcherClark, David J
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptUniversity of Melbourne Clinical School-
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