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The presence of bystander coronary artery disease invalidates a diagnosis of stress cardiomyopathy.
Stress cardiomyopathy affects both sexes equally.
Uniformly a preceding trigger leads to stress cardiomyopathy.
Stress cardiomyopathy (SCM) is a generally reversible acute cardiac syndrome that was originally described in the Japanese population over 30 years ago.
Hence, the term takotsubo (an octopus trap with a narrow neck and round bottom) cardiomyopathy ( Fig. 9.1 ).
SCM is also known as apical ballooning syndrome (ABS) and broken heart syndrome.
The clinical features mimic acute coronary syndrome (ACS).
The typical patient is a postmenopausal woman with symptoms of myocardial ischemia following a stressful event, with positive cardiac biomarkers and/or an electrocardiogram (ECG) demonstrating ischemia.
SCM is the final diagnosis in approximately 1% to 2% of all patients initially suspected of ACS, and in up to 12% in women with ST elevation myocardial infarction (STEMI) and in 8% of patients with cardiogenic shock.
Approximately 90% of all cases are in postmenopausal women.
Patients who are conscious typically have symptoms that are similar to those associated with MI, with angina-like chest pain, present in approximately 50% of cases; less common symptoms include dyspnea, syncope, or loss of consciousness from cardiac arrest.
Typically, the ejection fraction is reduced to 30% to 40%, which may be accompanied by significant diastolic dysfunction and elevated left ventricular end-diastolic pressure (LVEDP).
Acute heart failure is a frequent complication, and cardiogenic shock may develop in approximately 10% to 15% of patients.
Atrial fibrillation occurs in 5% of cases, whereas ventricular tachyarrhythmias have been reported in 3% to 4% of patients and asystole in 0.5%.
Rare complications include LV thrombus, thromboembolism, and cardiac rupture.
Hypotension may be owing to the reduction in stroke volume and, in some cases, dynamic left ventricular outflow tract obstruction (LVOTO).
The ventricular dysfunction usually resolves over days to weeks, with complete recovery by 4 to 8 weeks.
The prognosis of SCM is good in the absence of significant underlying comorbid conditions.
In-hospital mortality is approximately 3% to 5%.
The subgroup of patients in whom there is a physical trigger—such as major surgery, malignancy, and fractures—appears to have a worse prognosis.
The recurrence rate is approximately 1% to 2% per year.
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