Sections View Full Chapter Figures Tables Videos Annotate Full Chapter Figures Tables Videos Supplementary Content +++ ISCHEMIC HEART DISEASE +++ Stable coronary artery disease (CAD) ++ Types: Asymptomatic CAD or stable angina (angina that occurs reliably with exertion and emotional stress, relived with rest or nitroglycerin; due to fixed atherosclerosis) Diagnosis: Stress testing; computed tomography angiography (CCTA) vs. invasive coronary angiogram to assess anatomy Workup: HgA1c, lipid panel, ECG, TTE to assess LV function Treatment: - Address risk factors and disease pathology: Smoking cessation Exercise/weight loss/diet Control hypertension (goal at least <140/90 mmHg), ACEi (or ARB if intolerant of ACEi) Treat DM (preferably with SGLT2 inhibitors or GLP-1 agonists) Treat HLD, start statin (e.g., atorvastatin, rosuvastatin; goal LDL <70 mg/dL) - Consider addition of ezetimibe if LDL not at goal (IMPROVE-IT 2015) - Consider addition of PCSK9 inhibitor if LDL still not at goal and/or family history (FOURIER 2018) - Consider addition of icosapent ethyl if fasting triglycerides >135 mg/dL in patients with known CAD or DM (REDUCE-IT 2019) Aspirin (particularly if prior ACS event) Beta blocker (BB) (particularly if prior ACS event) - Address symptoms (antianginal therapy for stable angina): Beta blocker (BB): Increases coronary blood supply (↓HR → ↑coronary diastolic filling time → ↑blood supply) and decreases myocardial demand (↓contractility → ↓wall stress/O2 demand) Calcium channel blocker (CCB): If second agent required; similar mechanism as BB Nitrates: Vasodilation of coronary arteries; venodilation → ↓preload → ↓wall stress/O2 demand - Nitroglycerin (sublingual/transdermal/spray; taken as needed) - Isosorbide dinitrate (oral; taken BID or TID) - Isosorbide 5-mononitrate (oral; taken daily or BID) Ranolazine: Inhibits late inward sodium current in ischemic myocytes (Phase 0) → ↓Ca2+ overload → ↓wall stress/O2 demand and ↑coronary blood flow. Revascularization: Consider in patients who are symptomatic despite optimal medical therapy; only revascularize physiologically significant lesions as identified by stress testing or fractional flow reserve (FAME 2 2012; ISCHEMIA 2020). - EXCEPTIONS: Revascularization has mortality benefit in: Significant left main disease (i.e., >50% stenosis LAD): All patients should be revascularized; CABG vs. PCI depends on anatomic complexity and surgical candidacy; decision should be made after multidisciplinary review. Significant 3-vessel CAD (i.e., >70% stenosis in 3 vessels): All patients should be revascularized; CABG preferred to PCI in patients who are good surgical candidates (SYNTAX 2009), especially in patients with diabetes (FREEDOM 2012). HFrEF: Consider revascularization, especially if severe CAD or viable myocardium (limited data, though may have long-term benefit). +++ Myocardial infarction ++ Type I MI: Spontaneous MI (aka acute coronary syndrome from thrombus in a coronary artery) (Figure 1.13) - ACS without ST elevation (NSTEMI) NSTEMI: Subendocardial ischemia - Criteria: Rise and/or fall in troponin (Table 1.6) AND at least one of the following: Symptoms of acute myocardial ischemia New ischemic ECG changes (e.g., significant ST-T changes or LBBB) Development of pathologic Q waves Imaging evidence of loss of myocardial function ... Your Access profile is currently affiliated with [InstitutionA] and is in the process of switching affiliations to [InstitutionB]. Please select how you would like to proceed. Keep the current affiliation with [InstitutionA] and continue with the Access profile sign in process Switch affiliation to [InstitutionB] and continue with the Access profile sign in process Get Free Access Through Your Institution Learn how to see if your library subscribes to McGraw Hill Medical products. Subscribe: Institutional or Individual Sign In Error: Incorrect UserName or Password Username Error: Please enter User Name Password Error: Please enter Password Sign in Forgot Password? Forgot Username? Download the Access App: iOS | Android Sign in via OpenAthens Sign in via Shibboleth You already have access! Please proceed to your institution's subscription. Create a free profile for additional features.