Acute Management of Stress Cardiomyopathy (Takotsubo Syndrome)
Start ACE inhibitors or ARBs immediately as the cornerstone of acute management, as they facilitate left ventricular recovery and improve 1-year survival. 1
Initial Hemodynamic Assessment
The first critical step is to promptly evaluate for left ventricular outflow tract obstruction (LVOTO) using continuous wave Doppler echocardiography or LV pressure recording during angiography, as approximately 20% of patients with cardiogenic shock will have LVOTO, particularly those with apical ballooning. 1 This assessment must occur before administering any inotropic agents, as the presence or absence of LVOTO completely changes your management strategy. 1
Hemodynamically Stable Patients
Pharmacologic Therapy
ACE inhibitors or ARBs are the first-line agents and should be initiated immediately, as the European Society of Cardiology identifies these as the cornerstone of acute management. 1
Beta-blockers may be reasonable until full recovery of LVEF given the elevated catecholamine levels that drive this syndrome, but use them with extreme caution if QTc >500 ms or significant bradycardia is present due to risk of pause-dependent torsades de pointes. 1
Aspirin may be considered as part of supportive care. 1
Anticoagulation Strategy
Initiate IV or subcutaneous heparin when LV thrombus is detected or when severe LV dysfunction creates high thrombus risk. 1
Consider moderate-intensity warfarin (INR 2.0-3.0) for at least 3 months if acute LV thrombus is identified. 2, 1
Hemodynamically Unstable Patients Without LVOTO
If LVOTO has been excluded by echocardiography:
Levosimendan (calcium-sensitizer) is the preferred and safest inotrope and should be your first choice for pharmacologic support. 1
Catecholamines (dobutamine, norepinephrine, dopamine) may be used only with extreme caution if levosimendan is unavailable, as they are associated with 20% mortality in this setting. 1 Serial Doppler assessments are mandatory when catecholamines are administered because they can produce an evolving LVOT gradient. 1
Hemodynamically Unstable Patients With LVOTO
If LVOTO is present:
Intra-aortic balloon pump (IABP) is the first-line therapy for cardiogenic shock, as it supports blood pressure without increasing the obstruction gradient. 1
Pure vasopressors such as phenylephrine or vasopressin are preferred to maintain arterial pressure without worsening the LVOT gradient. 1
All traditional catecholamine inotropes, milrinone, nitroglycerin, and other vasodilators are absolutely contraindicated, as they increase the LVOT gradient and can be lethal. 1
Arrhythmia Management
Monitor continuously for new-onset atrial fibrillation, sinus node dysfunction, and AV block. 2
Consider a wearable defibrillator (life vest) for excessive QT prolongation or life-threatening ventricular arrhythmias, as malignant ventricular arrhythmias most frequently occur on hospital days 2-4. 1
Consider a temporary transvenous pacemaker for hemodynamically significant bradycardia. 1
Avoid QT-prolonging medications entirely in the acute phase. 1
Critical Pitfalls to Avoid
Never administer catecholamine-based inotropes as first-line therapy—they worsen the condition and carry 20% mortality. 1
Never give nitroglycerin if LVOTO is present—it aggravates the pressure gradient across the outflow tract. 1
Never start any inotropic agent before LVOTO has been excluded with Doppler echocardiography. 1
Never use beta-blockers in acute severe heart failure with markedly reduced ejection fraction and hypotension. 1
Monitoring Requirements
Serial echocardiography is essential to monitor LV function recovery, which typically occurs within 1-4 weeks. 1
Continuous telemetry monitoring is required throughout hospitalization, with heightened vigilance on days 2-4 when malignant arrhythmias peak. 1
Serial Doppler assessments are mandatory if catecholamines are used, as they can produce evolving LVOT gradients. 1
Transition to Long-Term Management
Continue ACE inhibitors or ARBs long-term, as they are associated with improved survival and may reduce the 5% recurrence rate. 2, 1
Beta-blockers have shown no evidence of survival benefit for long-term use and should not be relied upon for recurrence prevention. 1
Document complete recovery of LV function to confirm the diagnosis, as reversible myocardial dysfunction is the hallmark feature. 1