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1.
Am Fam Physician ; 83(7): 819-26, 2011 Apr 01.
Article in English | MEDLINE | ID: mdl-21524048

ABSTRACT

All patients with stable coronary artery disease require medical therapy to prevent disease progression and recurrent cardiovascular events. Three classes of medication are essential to therapy: lipid-lowering, antihypertensive, and antiplatelet agents. Lipid-lowering therapy is necessary to decrease low-density lipoprotein cholesterol to a target level of less than 100 mg per dL, and physicians should consider a goal of less than 70 mg per dL for very high-risk patients. Statins have demonstrated clear benefits in morbidity and mortality in the secondary prevention of coronary artery disease; other medications that can be used in addition to statins to lower cholesterol include ezetimibe, fibrates, and nicotinic acid. Blood pressure therapy for patients with coronary artery disease should start with beta blockers and angiotensin-converting enzyme inhibitors. If these medications are not tolerated, calcium channel blockers or angiotensin receptor blockers are acceptable alternatives. Aspirin is the first-line antiplatelet agent except in patients who have recently had a myocardial infarction or undergone stent placement, in which case clopidogrel is recommended. Anginal symptoms of coronary artery disease can be treated with beta blockers, calcium channel blockers, nitrates, or any combination of these. Familiarity with these medications and with the evidence supporting their use is essential to reducing morbidity and mortality in patients with coronary artery disease.


Subject(s)
Coronary Artery Disease , Adrenergic beta-Antagonists/administration & dosage , Adrenergic beta-Antagonists/adverse effects , Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Angiotensin-Converting Enzyme Inhibitors/adverse effects , Arterial Pressure/drug effects , Calcium Channel Blockers/administration & dosage , Calcium Channel Blockers/adverse effects , Clinical Protocols , Coronary Artery Disease/metabolism , Coronary Artery Disease/physiopathology , Coronary Artery Disease/psychology , Coronary Artery Disease/therapy , Humans , Hypolipidemic Agents/administration & dosage , Hypolipidemic Agents/adverse effects , Lipid Metabolism/drug effects , Lipoproteins, LDL/blood , Medication Therapy Management , Outcome Assessment, Health Care , Platelet Aggregation/drug effects , Platelet Aggregation Inhibitors/administration & dosage , Platelet Aggregation Inhibitors/adverse effects , Practice Guidelines as Topic , Risk Reduction Behavior , Secondary Prevention , Survival Analysis , Treatment Outcome
2.
J Am Coll Cardiol ; 56(4): 264-71, 2010 Jul 20.
Article in English | MEDLINE | ID: mdl-20493653

ABSTRACT

OBJECTIVES: The aim of this study was to evaluate the safety and efficacy of the novel platinum chromium TAXUS Element paclitaxel-eluting stent (PES) compared with the TAXUS Express PES (Boston Scientific, Natick, Massachusetts) in treating coronary artery stenoses. BACKGROUND: The TAXUS Element is a novel thin-strut (81 microm), platinum chromium alloy PES designed to improve radial strength, radiopacity, and deliverability, while safely providing comparable restenosis benefit compared with a previous-generation PES. METHODS: The PERSEUS (Prospective Evaluation in a Randomized Trial of the Safety and Efficacy of the Use of the TAXUS Element Paclitaxel-Eluting Coronary Stent System) Workhorse (WH) trial is a prospective, randomized (3:1), controlled, multicenter study of the TAXUS Element (vs. TAXUS Express) PES for the treatment of de novo coronary atherosclerotic lesionsor=2.75 to

Subject(s)
Chromium Alloys/administration & dosage , Coronary Angiography/standards , Coronary Stenosis/diagnostic imaging , Coronary Stenosis/drug therapy , Drug-Eluting Stents/standards , Paclitaxel/administration & dosage , Aged , Chromium/administration & dosage , Chromium/adverse effects , Chromium Alloys/adverse effects , Drug-Eluting Stents/adverse effects , Female , Follow-Up Studies , Humans , Male , Middle Aged , Paclitaxel/adverse effects , Platinum/administration & dosage , Platinum/adverse effects , Prospective Studies , Single-Blind Method , Treatment Outcome
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