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30 Cards in this Set
- Front
- Back
COURAGE trial
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contemporary PCI combined with aggressive medical therapy was not superior to aggressive medical therapy alone in reducing death or MI
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BARI-2D trial
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randomized type 2 DM with class I or II angina to revascularization (PCI or surgery) vs medical therapy; no difference in all-cause mortality or MI at 5 years
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coronary angiography and PCI should be reserved for
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symptomatic despite optimal medical therapy, unable to tolerate medications, high-risk findings on noninvasive imaging
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Indications for surgical revascularization in CAD
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left main disease and multivessel disease (2-3 vessels) with involvement of proximal LAD and reduced systolic function
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What is "hybrid" coronary revascularization?
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combining minimally invasive surgery and PCI; to reduce operative risk
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s/p PCI, duration of plavix (CSAP)
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1 year after DES, 1 month after BMS
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s/p PCI, duration of plavix (ACS)
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1 year
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s/p CABG duration of plavix
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CSAP not indicated, ACS 1 year
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elective noncardiac surgery in patients with CAD + stent - how long to delay surgery?
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at least 6 weeks after BMS; at least 1 year after DES
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use of TIMI risk score
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to determine aggressive medical therapy vs early invasive approach (>/=3 vs 0-2)
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how long should surgical revascularization be delayed after stopping clopidogrel?
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5-7 days
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advantages of prasugrel over clopidogrel? "PRESUGREL"
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recently approved oral thienopyridine that does not require hepatic conversion to its active form and is more potent with a faster onset than clopidogrel
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MOA of glycoprotein IIb/IIIa inhibitors
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block the final common pathway of platelet aggregation
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trade name of prasugrel
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Effient
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benefit most from glycoprotein IIb/IIIa inhibitors
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intermediate or high TIMI risk score and patients who undergo an early invasive approach and receive PCI
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ACUITY and the EARLY ACS trials
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increased bleeding events and no benefit for routine early glycoprotein IIb/IIIa inhibitors in ED
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when is LMWH preferred as anticoagulation ?
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the absence of kidney disease, in planned surgical revascularization, and in those undergoing an early invasive approach
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When is UFH preferred as anticoagulation
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for patients being considered for an early invasive approach, those with increased bleeding risk, and in the setting of kidney disease
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when is bivaluridin an acceptable alternative to UFH?
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patients undergoing elective PCI
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The MIRACL and PROVE IT trials found that
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high-dose statin therapy initiated soon after an ACS reduced cardiovascular events at 18 months and 2 years, respectively.
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Code STEMI time goals
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PCI within 90 mins of first medical contact; if not, thrombolytics within 30 mins
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target plasma glucose in patients hospitalized with ACS
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<180
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High-risk features in patients with STEMI (8)
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cardiogenic shock, new LBBB, anterior wall MI, HF, extensive ST-segment elevation, SBP <100 mm Hg, HR>100/min, and >75 years
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therapy for high-risk patient presents to a non–PCI-capable facility
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thrombolytic therapy and immediate transfer (no waiting to determine if reperfusion has occurred)
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therapy for patients with cardiogenic shock who present to a non–PCI-capable facility
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thrombolytic therapy, placement of an intra-aortic balloon pump, and immediate transfer to a PCI facility
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guideline-suggested door-to-balloon time
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<90 minutes
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what is "rescue" PCI?
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PCI performed in the setting of failed thrombolytic therapy
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What is "facilitated" PCI?
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strategy of planned, immediate PCI after full- or half-dose thrombolytic therapy +/- glycoprotein IIb/IIIa inhibitor
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rescue PCI or facilitated PCI of use?
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rescue PCI has benefit over conservative therapy or repeat thrombolytics; facilitated PCi should be avoided (increased adverse events)
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vascular complications of PCI (4)
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hematoma, arterial pseudoaneurysm, arteriovenous fistula, and retroperitoneal bleeding
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