(Acute Coronary Insufficiency; Preinfarction Angina; Intermediate Syndrome)
Unstable angina results from acute obstruction of a coronary artery without myocardial infarction. Symptoms include chest discomfort with or without dyspnea, nausea, and diaphoresis. Diagnosis is by ECG and the presence or absence of serologic markers. Treatment is with antiplatelet drugs, anticoagulants, nitrates, statins, and beta-blockers. Coronary angiography with percutaneous intervention or coronary artery bypass surgery is often necessary.
(See also Overview of Acute Coronary Syndromes.)
Rest angina that is prolonged (usually > 20 min)
New-onset angina of at least class 3 severity in the Canadian Cardiovascular Society (CCS) classification (see Table: Canadian Cardiovascular Society Classification System of Angina Pectoris)
Increasing angina, ie, previously diagnosed angina that has become distinctly more frequent, more severe, longer in duration, or lower in threshold (eg, increased by ≥ 1 CCS class or to at least CCS class 3)
Unstable angina is clinically unstable and often a prelude to MI or arrhythmias or, less commonly, to sudden death.
Patients have symptoms of angina pectoris (typically chest pain or discomfort) except that the pain or discomfort of unstable angina usually is more intense, lasts longer, is precipitated by less exertion, occurs spontaneously at rest (as angina decubitus), is progressive (crescendo) in nature, or involves any combination of these features.
Unstable angina is classified based on severity and clinical situation (see Table: Braunwald Classification of Unstable Angina*). Also considered are whether unstable angina occurs during treatment for chronic stable angina and whether transient changes in ST-T waves occur during angina. If angina has occurred within 48 h and no contributory extracardiac condition is present, troponin levels may be measured to help estimate prognosis; troponin-negative results indicate a better prognosis than troponin-positive.
Braunwald Classification of Unstable Angina*
(See figure: Approach to unstable angina.)
Evaluation begins with initial and serial ECG and serial measurements of cardiac markers to help distinguish between unstable angina and acute myocardial infarction (MI)—either non–ST-segment elevation MI (NSTEMI) or ST-segment elevation MI (STEMI). This distinction is the center of the decision pathway because fibrinolytics benefit patients with STEMI but may increase risk for those with NSTEMI and unstable angina. Also, urgent cardiac catheterization is indicated for patients with acute STEMI but not generally for those with NSTEMI or unstable angina.
ECG is the most important test and should be done within 10 min of presentation. ECG changes such as ST-segment depression, ST-segment elevation, or T-wave inversion may occur during unstable angina but are transient.
Patients suspected of having unstable angina should have a highly sensitive assay of cardiac troponin (hs-cTn) done on presentation and 3 h later (at 0 and 6 h if using a standard Tn assay). Of cardiac markers, CK is not elevated but cardiac troponin, particularly when measured using high-sensitivity troponin tests (hs-cTn), may be slightly increased but do not meet criteria for myocardial infarction (above the 99th percentile of the upper reference limit or URL).
Patients with unstable angina whose symptoms have resolved typically undergo angiography within the first 24 to 48 h of hospitalization to detect lesions that may require treatment. Coronary angiography most often combines diagnosis with percutaneous coronary intervention (PCI—ie, angioplasty, stent placement).
After initial evaluation and therapy, coronary angiography may be used in patients with evidence of ongoing ischemia (ECG findings or symptoms), hemodynamic instability, recurrent ventricular tachyarrhythmias, and other abnormalities that suggest recurrence of ischemic events.
Prognosis after an episode of unstable angina depends upon how many coronary arteries are diseased, which arteries are affected, and how severely they are affected. For example, stenosis of the proximal left main artery or equivalent (proximal left arterial descending and circumflex artery stenosis) have a worse prognosis than does distal stenosis or stenosis in a smaller arterial branch. Left ventricular function also greatly influences prognosis; patients with significant left ventricular dysfunction (even those with 1- or 2-vessel disease) would have a lower threshold for revascularization.
Overall, about 30% of patients with unstable angina have an MI within 3 mo of onset; sudden death is less common. Marked ECG changes with chest pain indicate higher risk of subsequent MI or death.
Prehospital care: Oxygen, aspirin, nitrates and/or opioids for pain, and triage to an appropriate medical center
Drug treatment: Antiplatelet drugs, antianginal drugs, anticoagulants, and in some cases other drugs)
Angiography to assess coronary artery anatomy
Reperfusion therapy: Percutaneous coronary intervention or coronary artery bypass surgery
Post discharge rehabilitation and chronic medical management of coronary artery disease
A reliable IV route must be established, oxygen given (typically 2 L by nasal cannula), and continuous single-lead ECG monitoring started. Prehospital interventions by emergency medical personnel (including ECG, chewed aspirin [325 mg], pain management with nitrates or opioids) can reduce risk of mortality and complications. Early diagnostic data and response to treatment can help determine the need for and timing of revascularization.
On arrival to the emergency room, the patient's diagnosis is confirmed. Drug therapy and timing of revascularization depend on the clinical picture. In clinically unstable patients (patients with ongoing symptoms, hypotension or sustained arrhythmias), urgent angiography with revascularization is indicated. In clinically stable patients, angiography with revascularization may be deferred for 24 to 48 h (see Figure: Approach to unstable angina.).
Approach to unstable angina.
All patients should be given antiplatelet drugs, anticoagulants, and if chest pain is present, antianginals. The specific drugs used depend on the reperfusion strategy and other factors; their selection and use is discussed in Drugs for Acute Coronary Syndrome. Other drugs, such as beta-blockers, ACE inhibitors, and statins, should be initiated during admission (see Table: Drugs for Coronary Artery Disease*).
Patients with unstable angina should be given the following (unless contraindicated)
Antiplatelet drugs: Aspirin, clopidogrel, or both (prasugrel or ticagrelor are alternatives to clopidogrel)
Anticoagulants: A heparin (unfractionated or low molecular weight heparin) or bivalirudin
Glycoprotein IIb/IIIa inhibitor for some high-risk patients
Antianginal therapy usually nitroglycerin
All patients are given aspirin 160 to 325 mg (not enteric-coated), if not contraindicated, at presentation and 81 mg once/day indefinitely thereafter. Chewing the first dose before swallowing quickens absorption. Aspirin reduces short- and long-term mortality risk. In patients undergoing PCI, a loading dose of clopidogrel (300 to 600 mg po once), prasugrel (60 mg po once), or ticagrelor (180 mg po once) improves outcomes, particularly when administered 24 h in advance. For urgent PCI, prasugrel and ticagrelor are more rapid in onset and may be preferred.
Either a low molecular weight heparin (LMWH), unfractionated heparin, or bivalirudin is given routinely to patients with unstable angina unless contraindicated (eg, by active bleeding). Unfractionated heparin is more complicated to use because it requires frequent (q 6 h) dosing adjustments to achieve target activated PTT (aPTT). The LMWHs have better bioavailability, are given by simple weight-based dose without monitoring aPTT and dose titration, and have lower risk of heparin-induced thrombocytopenia. Bivalirudin is recommended for those with a known or suspected history of heparin-induced thrombocytopenia.
Consider glycoprotein IIb/IIIa inhibitor for high risk patients (patients with recurrent ischemia, dynamic ECG changes or hemodynamic instability). Abciximab, tirofiban, and eptifibatide appear to have equivalent efficacy, and the choice of drug should depend on other factors (eg, cost, availability, familiarity).
Chest pain can be treated with morphine or nitroglycerin. Morphine 2 to 4 mg IV, repeated q 15 min as needed, is highly effective but can depress respiration, can reduce myocardial contractility, and is a potent venous vasodilator. Hypotension and bradycardia secondary to morphine can usually be overcome by prompt elevation of the lower extremities. Nitroglycerin is initially given sublingually, followed by continuous IV drip if needed.
Standard therapy for all patients with unstable angina includes beta-blockers, ACE inhibitors, and statins. Beta-blockers are recommended unless contraindicated (eg, by bradycardia, heart block, hypotension, or asthma), especially for high-risk patients. Beta-blockers reduce heart rate, arterial pressure, and contractility, thereby reducing cardiac workload and oxygen demand. ACE inhibitors may provide long-term cardioprotection by improving endothelial function. If an ACE inhibitor is not tolerated because of cough or rash (but not angioedema or renal dysfunction), an angiotensin II receptor blocker may be substituted. Statins are also standard therapy and should be continued indefinitely.
Fibrinolytic drugs, which can be helpful in patients with STEMI, do not benefit patients with unstable angina.
Angiography is typically done during admission—within 24 to 48 h of admission if the patient is stable or immediately in unstable patients (eg, with ongoing symptoms, hypotension, sustained arrhythmias). Angiographic findings help determine whether PCI or CABG is indicated. Choice of reperfusion strategy is further discussed in Revascularization for Acute Coronary Syndromes.
Patients who did not have coronary angiography during admission, have no high-risk features (eg, heart failure, recurrent angina, VT or VF after 24 h, mechanical complications such as new murmurs, shock), and have an ejection fraction > 40% usually should have stress testing of some sort before or shortly after discharge.
The acute illness and treatment of unstable angina should be used to strongly motivate the patient to modify risk factors. Evaluating the patient’s physical and emotional status and discussing them with the patient, advising about lifestyle (eg, smoking, diet, work and play habits, exercise), and aggressively managing risk factors may improve prognosis.
On discharge, all patients should be continued on appropriate antiplatelet drugs, statins, antianginals, and other drugs based on comorbidities.
Unstable angina is new, worsening, or rest angina in patients whose cardiac biomarkers do not meet criteria for myocardial infarction.
Symptoms of unstable angina include new or worsening chest pain or chest pain occurring at rest.
Diagnosis is based on serial ECGs and cardiac markers.
Immediate treatment includes oxygen, antianginals, antiplatelet drugs, and anticoagulants.
For patients with ongoing symptoms, hypotension or sustained arrhythmias, do immediate angiography.
For stable patients, do angiography within 24 to 48 h of hospitalization.
Following recovery, initiate or continue antiplatelet drugs, beta-blockers, ACE inhibitors, and statins.