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dc.contributor.authorYudi, M.
dc.contributor.authorEccleston, D.
dc.contributor.authorAndrianpoulos, N.
dc.contributor.authorFarouque, O.
dc.contributor.authorDuffy, S.
dc.contributor.authorBrennan, A.
dc.contributor.authorReid, Christopher
dc.contributor.authorClark, D.
dc.contributor.authorAjani, A.
dc.date.accessioned2017-01-30T15:34:17Z
dc.date.available2017-01-30T15:34:17Z
dc.date.created2015-07-16T06:21:52Z
dc.date.issued2015
dc.identifier.citationYudi, M. and Eccleston, D. and Andrianpoulos, N. and Farouque, O. and Duffy, S. and Brennan, A. and Reid, C. et al. 2015. Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention. Internal Medicine Journal. 45 (10): pp. 1032-1037.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/47581
dc.identifier.doi10.1111/imj.12818
dc.description.abstract

Background - Although dual antiplatelet therapy is the standard of care in non-ST-segment elevation acute coronary syndromes (NSTEACS), it remains unclear when a second antiplatelet agent should be initiated. We sought to assess the safety and efficacy of pretreatment with clopidogrel in patients with NSTEACS undergoing percutaneous coronary intervention (PCI). Methods - We analyzed baseline clinical and procedural characteristics of 6,817 patients with NSTEACS who underwent PCI from the Melbourne Interventional Group registry from 2005-2012. Patients were included in the pretreatment group if clopidogrel was administered prior to cardiac catheterisation. We assessed 30-day mortality, myocardial infarction (MI) and major adverse cardiovascular events (MACE). The safety endpoint was in-hospital bleeding. Results - Of the 6,817 patients, only 2,951 (43%) received pretreatment with clopidogrel. Patients in the pretreatment group were more likely to present with unstable angina (70.8% vs. 68.2%, p=0.02) and have a history of myocardial infarction (35.6% vs. 23.6%, p < 0.01) but were less likely to have PCI within 24 hours of admission (17.2% vs. 25.2%, p <0.01). There was no difference between the groups in 30-day mortality (0.9% vs. 1.4%, p=0.06), MI (2.0% vs. 2.2%, p=0.52) or MACE (3.7% vs. 4.2%, p=0.25). There was no difference in bleeding complications (1.9% vs. 1.9%, p=0.94). Conclusions - Pretreatment with dual antiplatelet therapy in NSTEACS is not routine clinical practice in Australia. Pretreatment appears safe but is not associated with improved short-term clinical outcomes.

dc.publisherBlackwell Publishing
dc.titlePretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
dc.typeJournal Article
dcterms.source.volumexx
dcterms.source.startPagexx
dcterms.source.endPagexx
dcterms.source.issn14440903
dcterms.source.titleInternal Medicine Journal
curtin.accessStatusFulltext not available


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