Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22215
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dc.contributor.authorGellatly, Rochelle M-
dc.contributor.authorConnell, Cia-
dc.contributor.authorTan, Christianne-
dc.contributor.authorAndrianopoulos, Nick-
dc.contributor.authorAjani, Andrew E-
dc.contributor.authorClark, David J-
dc.contributor.authorNanayakkara, Shane-
dc.contributor.authorSebastian, Martin-
dc.contributor.authorBrennan, Angela-
dc.contributor.authorFreeman, Melanie-
dc.contributor.authorO'Brien, Jessica-
dc.contributor.authorSelkrig, Laura A-
dc.contributor.authorReid, Christopher M-
dc.contributor.authorDuffy, Stephen J-
dc.date2019-11-25-
dc.date.accessioned2019-12-04T05:00:32Z-
dc.date.available2019-12-04T05:00:32Z-
dc.date.issued2020-05-
dc.identifier.citationThe Annals of Pharmacotherapy 2020; 54(5): 414-422en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22215-
dc.description.abstractBackground: Glycoprotein IIb/IIIa inhibitors (GPIs) are a treatment option in the management of acute coronary syndromes (ACSs). Evidence supporting the use of GPIs predates trials establishing the benefits of P2Y12 inhibitors, routine early invasive therapy, and thrombectomy devices in patients with ACS. Objective: The aim of this study was to determine trends in GPI use and their associated outcomes in contemporary practice. Methods: We assessed GPI use in patients with ACS undergoing percutaneous coronary intervention (PCI) from the Melbourne Interventional Group registry (2005-2013). The primary endpoint was the 30-day incidence of major adverse cardiovascular events (MACE). The safety endpoint was in-hospital major bleeding. Results: GPIs were used in 40.5% of 12 357 patients with ACS undergoing PCI. GPI use decreased over the study period (P for trend <0.0001). Patients were more likely to receive GPIs if they were younger, presented with a ST-elevation myocardial infarction (STEMI), had more complex (B2/C-type) lesions, and when thrombectomy devices were used (all P < 0.0001). MACE were higher in patients receiving GPI (4.9% vs 4.1%, P = 0.03). Propensity score matching revealed no difference in 30-day mortality and 30-day MACE (odds ratio [OR] = 1.00; 95% CI = 0.99-1.004 and OR = 1.01; 95% CI = 0.99-1.02, respectively). GPI use was associated with more bleeding complications (3.6% vs 1.8%, P < 0.0001). Conclusion and Relevance: GPI use in ACS patients undergoing PCI has declined, and use appears to be dictated by ACS type and lesion complexity, as opposed to high-risk comorbidities. GPI use was associated with a doubling in bleeding complications.en_US
dc.language.isoeng-
dc.subjectacute coronary syndromeen_US
dc.subjectbleedingen_US
dc.subjectdrugsen_US
dc.subjectglycoprotein-IIb/IIIa inhibitorsen_US
dc.subjectpercutaneous coronary interventionen_US
dc.titleTrends of Use and Outcomes Associated With Glycoprotein-IIb/IIIa Inhibitors in Patients With Acute Coronary Syndromes Undergoing Percutaneous Coronary Intervention.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe Annals of Pharmacotherapyen_US
dc.identifier.affiliationAlfred Hospital, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationMonash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationRoyal Melbourne Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationThe University of Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationUniversity Hospital Geelong, Victoria, Australiaen_US
dc.identifier.affiliationBox Hill Hospital, Victoria, Australiaen_US
dc.identifier.doi10.1177/1060028019889550en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-4518-5948en_US
dc.identifier.pubmedid31766865-
dc.type.austinJournal Article-
local.name.researcherClark, David J
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptCardiology-
crisitem.author.deptUniversity of Melbourne Clinical School-
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