Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16968
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dc.contributor.authorTheuerle, James D-
dc.contributor.authorYudi, Matias B-
dc.contributor.authorFarouque, Omar-
dc.contributor.authorAndrianopoulos, Nick-
dc.contributor.authorScott, Peter-
dc.contributor.authorAjani, Andrew E-
dc.contributor.authorBrennan, Angela L-
dc.contributor.authorDuffy, Stephen J-
dc.contributor.authorReid, Christopher M-
dc.contributor.authorClark, David J-
dc.contributor.authorMelbourne Interventional Group-
dc.date2017-11-15-
dc.date.accessioned2017-11-27T03:31:40Z-
dc.date.available2017-11-27T03:31:40Z-
dc.date.issued2018-
dc.identifier.citationCatheterization & Cardiovascular Interventions 2018; 92(3): E227-E234en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16968-
dc.description.abstractBACKGROUND: Correlations between the ACC/AHA coronary lesion classification and clinical outcomes in the contemporary percutaneous coronary intervention (PCI) era are not well established. METHODS: We analyzed clinical characteristics and outcomes according to ACC/AHA lesion classification (A, B1, B2, C) in 13,701 consecutive patients from the Melbourne Interventional Group (MIG) registry. Patients presenting with STEMI, cardiogenic shock and out-of-hospital cardiac arrest were excluded. The primary endpoints were 30-day and 12-month mortality. Secondary endpoints were procedural success as well as 30-day and 12-month major adverse cardiac events. RESULTS: Of the 13,701 patients treated, 1,246 (9.1%) had type A lesions, 5,519 (40.3%) had type B1 lesions, 4,449 (32.5%) had Type B2 lesions and 2,487 (18.2%) had Type C lesions. Patients with type C lesions were more likely to be older and have impaired renal function, diabetes, previous myocardial infarction, peripheral vascular disease and prior bypass graft surgery (all P < 0.01). They were also more likely to require rotational atherectomy, drug-eluting stents and longer stent lengths (all P < 0.01). Increasing lesion complexity was associated with lower procedural success (99.6% vs. 99.1% vs. 96.6% vs. 82.7%, P < 0.001) and worse 30-day (0.2% vs. 0.3% vs. 0.7% vs. 0.6%, P < 0.001) and 12-month mortality (2.2% vs. 2.0% vs. 3.2% vs. 2.9%, P <0.01). Kaplan Meier analysis showed complex lesions (type B2 and C) had lower survival at 12-months (P = 0.003). CONCLUSIONS: PCI to more complex lesions continues to be associated with lower procedural success rates as well as inferior medium-term clinical outcomes. Thus the ACC/AHA lesion classification should still be calculated preprocedure to predict acute PCI success and clinical outcomes.en_US
dc.subjectLesion complexityen_US
dc.subjectPCIen_US
dc.subjectClinical outcomesen_US
dc.titleUtility of the ACC/AHA lesion classification as a predictor of procedural, 30-day and 12-month outcomes in the contemporary percutaneous coronary intervention eraen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCatheterization & Cardiovascular Interventionsen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationCentre of Cardiovascular Research and Education in Therapeutics (CCRE), Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Cardiology, Royal Melbourne Hospital, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Cardiovascular Medicine, Alfred Hospital, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationSchool of Public Health, Curtin University, Perth, WA, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/29139601en_US
dc.identifier.doi10.1002/ccd.27411en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherClark, David J
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptCardiology-
crisitem.author.deptUniversity of Melbourne Clinical School-
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