Takotsubo Syndrome: Optimizing Care with a Multidisciplinary Approach

Introduction

Takotsubo syndrome (TTS) was first described by Sato et al in 1990¹ and has also been called stress cardiomyopathy, broken heart syndrome, apical ballooning syndrome, left ventricle (LV) apical ballooning syndrome, Takotsubo cardiomyopathy, and transient apical ballooning syndrome. The name derives from the Japanese fishing pot “Takotsubo,” which is used to trap octopuses and has a form similar to the characteristic ballooning of the LV apex. Symptoms of TTS include acute and transient regional systolic dysfunction of the LV, as well as a variety of wall-motion abnormalities (WMAs).² The prognosis is generally considered to be favorable.

Although the clinical features—including initial symptoms, cardiac biomarkers, and electrocardiogram (ECG) changes—resemble those of acute coronary syndrome (ACS), there is no obvious obstructive coronary artery disease explaining the severity of the LV systolic and diastolic dysfunction. ECG and/or left ventriculography are commonly used to detect transient WMAs. The syndrome primarily affects elderly women. Emotional or physical stress³ and central nervous system (CNS) diseases are common triggers.⁴ Although the etiology of TTS remains unclear, exaggerated sympathetic stimulation, in association with dysfunction of the limbic system, has been reported to be related to TTS occurrence. Cancer also induces emotional and physical stress and a recent study demonstrated the strong association between TTS and malignant diseases.⁵ Therefore, TTS care optimization should involve cardiac, neurological, psychiatric, and oncological approaches. We present the current state of TTS knowledge and describe a multidisciplinary approach to optimize TTS care.

Epidemiology

A 2015 study reported that approximately 2% of patients initially suspected as having ACS in fact had TTS, and most of these cases were postmenopausal women aged ≥50 years.⁶ Another study found that up to 10% of female patients with TTS were initially suspected of having ACS.⁷ Schneider et al reported that approximately 90% of patients with TTS were middle-aged women, and approximately 80% were aged above 50.⁸ However, a more recent study by Topal et al concluded that TTS affects adults, children, and newborns alike, with no discernible sex differences.⁹ On the other hand, Templin et al reported that the etiology of TTS in women is more likely to involve emotional stress, while that in men is more likely to involve physical stress.² Compared with younger patients, elderly patients with TTS tend to show poor outcomes caused by stroke, severe arrhythmias, acute heart failure, and cardiogenic shock.¹⁰ Moreover, many younger patients have nonapical anatomical variants and severe LV dysfunction.¹¹

Singh et al discovered that TTS recurs within 6 months in 1.2% of patients and within 6 years in nearly 5%.¹² El-Battrawy et al analyzed the data from a multicenter registry and found that the TTS recurrence rate was approximately 4%.¹³ Kato et al analyzed the International Takotsubo (InterTAK) Registry and concluded that neurological and psychiatric diseases are predictors of TTS recurrence.¹⁴ Other possible predictors of TTS recurrence include hypertension¹³ and chronic obstructive pulmonary disease (COPD)¹⁵ are also possible predictors of TTS recurrence.

Pathogenic Mechanisms

Although the precise pathophysiological mechanisms of TTS are unknown, significant evidence suggests exaggerated sympathetic stimulation is involved.¹⁶ TTS is frequently preceded by physical and emotional stress.² Causes of catecholamine excess, such as pheochromocytoma,¹⁷ CNS disorders,¹⁸ and hyperactivity in specific cerebral regions, have been associated with this disease.¹⁹ In addition, intravenous catecholamine β-receptor agonist administration can cause TTS symptoms and various ballooning patterns.²⁰ A previous study showed that the catecholamine levels are more elevated in patients with TTS triggered by emotional stress than in patients with myocardial infarction (MI).²¹ In addition, Kume et al discovered that patients with TTS have high norepinephrine levels in the coronary sinus, which would reflect an increase of myocardial catecholamines.²² In a study by Ortak et al, the cardiac parasympathetic activity markedly declined in patients with acute phase TTS, followed by autonomic modulation recovery between the subacute and chronic phases.²³ According to a previous study with single-photon emission computed tomography (SPECT), patients with TTS showed cardiac uptake of the ¹²³I- metaiodobenzylguanidine (MIBG) uptake in the akinetic LV apex, with almost normal perfusion within this region assessed by the ^99mTc-MIBI SPECT.²⁴ Therefore, exaggerated sympathetic stimulation may have a great impact on the pathogenic mechanisms of TTS.

As mentioned above, exaggerated sympathetic stimulation is crucial for the pathogenic mechanisms of TTS. However, the mechanism by which exaggerated sympathetic stimulation causes myocardial stunning in various regional ballooning patterns that characterize TTS remains unclear. Researchers have proposed several hypotheses, such as activation of myocardial survival pathways, catecholamine toxicity on cardiomyocytes, microcirculatory dysfunction, multivessel epicardial spasm, inflammation, and plaque rupture.¹⁶ Considering the high occurrence rate of TTS in postmenopausal females, estrogen deficiency may be an important factor for the pathophysiology of TTS. Previous studies showed that estrogens reduce mental stress²⁵ and catecholamine-induced vasoconstriction.²⁶ However, there were no evidence of correlation between estrogen levels and TTS.²⁷ Clearly, further studies will be needed to elucidate the etiology of TTS.

Optimizing Care with a Multidisciplinary Approach

Optimizing Care with a Cardiac Approach

The first step in optimizing care is to diagnose TTS accurately via a cardiac approach. Multimodality imaging, including ECG, echocardiogram, angiography, ventriculography, and cardiac magnetic resonance (CMR) imaging, is indispensable for accurate diagnosis, management of therapy, and evaluation of prognosis. The diagnosis of TTS should be comprehensive; it should include diagnostic criteria and multimodality imaging.

ECG Findings

Increased heart rate, ST-segment elevation, and long QTc are the common ECG findings of TTS.² Kurisu et al examined the temporal features of ECG of patients with TTS,²⁸ and reported the following ECG features: (1) the normalization of ST-segment changes within 3 days; (2) the persistence of ECG changes; (3) the similarity of temporal features of the ECG to those of patients with minimal acute MI (AMI), and (4) patients with TTS showed deeper T-wave inversion and a longer QTc interval than patients with the minimal AMI group during the acute phase. Thus, the temporal changes in ECG in patients with TTS resemble those in patients with AMI. Physicians must take care to differentiate these cardiac disorders for effective patient management.

Biomarkers

Two types of biomarkers, namely, natriuretic peptides and cardiac myonecrosis markers, are commonly used for TTS diagnosis. At the time of diagnosis, the levels of plasma B-type natriuretic peptide (BNP)²⁹ or its precursor N-terminal pro–BNP (NT-proBNP)³⁰ are often high in patients with TTS. In contrast, patients with TTS typically show lower levels of the cardiac myonecrosis biomarkers cardiac troponin and creatine kinase-MB (CKMB) than patients with AMI, as tissue necrosis is mild or absent in patients with TTS.³¹ Relations between these biomarkers, including the troponin T/CKMB ratio,³² BNP/troponin I ratio,³³ and NT-pro–BNP/troponin T ratio,³⁴ may be useful for the differential diagnosis of TTS. However, in some cases, there are no significant differences in troponin levels between patients with TTS and patients with AMI. Moreover, in TTS, the degree of angiographic myocardial dysfunction differs from the extent of biomarker elevation.³⁵ Several other novel markers, such as copeptin, ischemic modified albumin, soluble lectin-like oxidized low density lipoprot receptor-1, and soluble suppression of tumorigenicity-2, may be possible biomarkers for TTS.³⁶

Echocardiography

Most patients with suspected TTS initially undergo a transthoracic echocardiogram.³⁷ This helps to detect the apical-midventricular ballooning and the WMA patterns. The echocardiogram also provides helpful information about contractile function and complications, including LV outflow tract obstruction (LVOTO; intraventricular gradient > 25 mmHg), LV thrombi, pericardial effusion, reversible moderate-to-severe mitral regurgitation, and right ventricular (RV) involvement. The RV involvement, though transient, leads to longer hospitalization and hemodynamic instability.³⁸

Contrast echocardiography is used to obtain accurate information on wall motion (apical, midventricular, or basal ballooning) and the existence of intraventricular thrombus in patients with a poor acoustic window.³⁷ In addition, 3D echocardiography is useful for quantifying chamber measurements, with higher accuracy and reproducibility than 2D echocardiography.³⁹ Compared with 2D echocardiography, 3D echocardiography provides more detailed information regarding the regional WMAs.⁴⁰ Moreover, 3D echocardiography may be useful for detecting the RV involvement, even in the acute phase. Finally, strain imaging using speckle tracking echocardiography may help assess the severity of RV involvement.⁴¹

Angiography and Ventriculography

As mentioned above, differentiating TTS from AMI is difficult, as the two conditions have similar clinical features, including the clinical course, ECG, and cardiac biomarkers.⁴² Compared to patients with AMI, most patients with TTS have higher troponin levels but similar ECG findings.² Moreover, patients with TTS frequently have coronary artery disease; this coexistence often leads to adverse outcomes,⁴³ but the coronary arteries of these patients often show almost normal findings. Therefore, early examination of the coronary arteries by angiography is important in order to exclude the possibility of ACS.

Echocardiography and left ventriculography are useful in assessing regional WMAs.¹⁶ All patients with suspected TTS should have LV ventriculography, since this modality can be used to diagnose TTS during cardiac catheterization.³⁷ Biplane left ventriculography can assess LV function and type of WMA, including by differentiating four morphological patterns of TTS, ie, apical TTS, midventricular TTS, basal TTS, and focal TTS.^37,44

CMR

CMR is used for the extensive assessment of structural and functional alterations of cardiac tissues of patients with TTS.⁴⁵ There are three CMR diagnostic criteria for TTS: conventional regional WMAs; the existence of reversible tissue injury (edema); and the absence of irreversible tissue injury (late gadolinium enhancement) when signal intensity thresholds of 5 standard deviations are applied.

The further merit of CMR is that it provides useful information regarding the differential diagnosis (MI and myocarditis), it provides pathophysiological information, and it can detect complications (eg, LV thrombi) for the managements of patients with TTS. CMR should be performed in the acute phase for patients with suspected TTS. In particular, it should be done if another type of MI with nonobstructive coronary arteries (eg, myocarditis) is suspected, and a different cardiac approach is required. In the chronic phase, all patients with TTS should be examined by CMR within 2 months, especially if abnormalities of ECG and/or echocardiographic findings persist, because such clinical courses are not typical of TTS.

Diagnostic Criteria for TTS

Currently, no single universally accepted diagnostic criteria are available for TTS; thus, several criteria have been proposed for diagnosing TTS. Among these criteria, the Mayo Clinic diagnostic criteria are perhaps the most well-established (Box 1).⁴² The Heart Failure Association diagnostic criteria for TTS are also well known (Box 2).^46,47 Another set of criteria, the InterTAK diagnostic criteria²⁷ incorporate several different aspects of TTS as follows: (i) RV and other atypical WMAs are involved; (ii) TTS is not necessarily accompanied by emotional or physical stress; (iii) potential triggers for TTS are neurological disorders and pheochromocytoma; and (iv) the coexistence of coronary artery disorder and TTS has been established (Box 3).

Box 1 Mayo Clinic Criteria for TTS

Box 2 Heart Failure Association Diagnostic Criteria for TTS

Box 3 International Takotsubo Diagnostic Criteria (InterTAK Diagnostic Criteria)

Moreover, the InterTAK Diagnostic Score is a clinical scoring method used to assess the probability of TTS and to differentiate TTS from ACS in the acute phase.⁴⁸ Based on the ECG findings and clinical course; this score consists of the following indices: female sex (25 points); emotional stress (24 points); physical stress (13 points); absence of ST-segment depression (12 points); acute, former, or chronic psychiatric disorder (11 points); acute, former, or chronic neurological disorders (9 points); and long QTc (6 points). Patients with InterTAK scores of ≥ 50 or ≤ 31 were almost always correctly diagnosed as having TTS or ACS, respectively.⁴⁸

Recommended Cardiac Approach for Acute-Phase TTS

Although TTS is considered benign, 21.8% of patients develop serious complications in the hospital.² Kato et al demonstrated that 40% of patients have in-hospital cardiac complications, including pulmonary edema and cardiogenic shock.⁴⁹ The current cardiac approach during the acute phase is thus primarily supportive, with the goal of preventing life-threatening complications.⁵⁰ Patients with long QTc should undergo ECG monitoring because they are at high risk for ventricular arrhythmias;⁵¹ therefore, ECG monitoring for at least one day is mandatory for all patients with TTS. Diagnosed TTS patients should be given supportive pharmacological treatment (eg, β-blockers, diuretics, anticoagulants, antiarrhythmics, and non-catecholamine inotropes such as levosimendan). Nonpharmacological support may include mechanical circulatory and respiratory support, depending on the grade of heart failure and concomitant complications. Among forms of mechanical circulatory support, intraaortic balloon pumps should not be used unless LVOTO has been ruled out.

If hemodynamically significant LVOTO is present, there may be hypercontractility of the basal segments, in which case inotropic drugs should be immediately stopped in order to avoid further obstruction. Short-acting intravenous β-blockers should be considered when patients have no severe heart failure. Esmolol, a cardioselective-1 blocker with a short half-life (9 minutes), may be a simple treatment option for patients with TTS and LVOTO. Santoro et al found in a case series of 10 patients with TTS and LVOTO that esmolol infusion ameliorated the reductions in intraventricular gradient and systemic blood pressure.⁵² Experimental data showed a high-density of β2-adrenergic receptors in the apical and midventricular segments of the LV, and a high-density of β1-adrenergic receptors in the basal LV segments.⁵³

Conversely, when there is cardiogenic shock without LVOTO, catecholamines (ie, inotropes) can be used to maintain pressure. Levosimendan, a catecholamine-sparing positive inotrope, may be a useful alternative,⁵⁴ although there is limited evidence supporting its use. Mechanical support should be considered early in the treatment of patients whose cardiac output is low. A microaxial blood pump may help as it has the advantage of not increasing the afterload.² If there are no contraindications, patients with refractory shock may require extracorporeal life support or a temporary LV assist device. The use of standard cardiac approaches to reduce preload in TTS patients with congestive heart failure (eg, diuretics and nitroglycerine) should be carefully considered. There is no positive evidence to support the routine use of β-blockers for the management of TTS during the acute phase.⁵⁵

A serious complication of TTS is intraventricular thrombus. It is seen in patients with severe WMAs and low LV ejection fraction (LVEF);^45,56 nearly 25% of patients with TTS suffer from this complication. Prophylactic anticoagulation should be considered for all patients with TTS to prevent LV apical thrombus formation.^57,58 A recent study demonstrated that the InterTAK Thrombus Risk Score (Table 1) is a useful tool to assess the risk for thrombus formation for patients with TTS.⁵⁹ This score consists of the following indices: apical type TTS (1.5 points); previous vascular disease (1.5 points); LVEF ≤ 30% on admission (1.5 points); and white blood cell counts on admission > 10,000 cells/μL (1 point). Patients with an InterTAK Thrombus Risk Score of ≥ 3 are considered to be at high risk of thrombus formation.

Table 1 Important Signs in TTS Patients Indicating a Need for Consultation with Specialists

Madias et al reported that nearly 9% of their patients with TTS had torsades de pointes or ventricular fibrillation, and long QTc was significantly correlated with ventricular arrhythmia occurrence.⁵¹ Temporary cardiac pacing at a high rate⁶⁰ or intravenous magnesium⁶¹ has been reported to be effective in preventing ventricular fibrillation recurrence. The need for an implantable cardioverter-defibrillator (ICD) for ventricular arrhythmia prevention in the acute phase remains unconfirmed; however, considering the reversible nature of TTS, ICD therapy may not be required.

Recommended Cardiac Approach for Chronic-Phase TTS

To date, the effectiveness of renin-angiotensin system inhibitors (RASi) such as angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers remains controversial. Templin et al showed that the use of RASi improved survival during the chronic phase.² In a meta-analysis by Singh et al, some of the studies found that RASi showed benefit.¹² These findings could be explained by a decrease in sympathetic activity via the RAS or an anti-inflammatory effect on the myocardium. On the other hand, Santoro et al found that RASi had no benefit,⁶² while Brunetti et al showed that RASi had benefit only when associated with a β-blocker.⁶³ Recent multicenter studies showed that RASi had no benefit^13,14 even when used in combination with a β-blocker.¹⁵

In addition, β-blockers may help to protect against catecholamine surges following stressful triggers. Indeed, β-blockers are a common discharge medication for TTS patients. However, there is no conclusive evidence regarding the effectiveness of β-blockers on mortality in the chronic-phase.² Two meta-analyses also showed that β-blockers had no preventive effect against TTS recurrence.^12,62 Hence, the effects of β-blockers during the chronic-phase might be more restrictive than expected.

In regard to the pathogenesis of TTS, the idea of using estrogen supplements to prevent recurrence is an intriguing one. However, no studies have investigated this. At the present time, estrogen supplementation is not recommended, as there is an increased risk for venous thromboembolism.

Optimizing Care with a Neurological Approach

TTS is frequently triggered by CNS diseases.⁴ Ischemic stroke, subarachnoid hemorrhage, and seizures are the best-known causes of TTS.¹⁶ Meanwhile, amyotrophic lateral sclerosis, encephalopathy syndrome, intracerebral bleeding, migraine, posterior reversible encephalitis/meningitis, and traumatic injury are rare triggers of TTS.⁴ In one case report, TTS was triggered by a possible limbic encephalopathy caused by high-grade B-cell lymphoma.⁶⁴ We have also recently reported a patient with TTS associated with autonomic limbic encephalitis.⁶⁵ Thus, neurological disorders are clearly associated with TTS occurrence.

Dysfunction of the Limbic System

While there is strong evidence to support the involvement of the brain–heart axis in TTS,⁶⁶ the pathological mechanism of TTS remains poorly understood. It has been hypothesized that exaggerated sympathetic stimulation plays a role in the etiology of TTS.²¹ The limbic system consists of several regions, such as the amygdala, cingulate cortex, hippocampus, and insula, and this system may have a role in regulating the autonomic nervous system.⁶⁷ According to a functional magnetic resonance imaging (MRI) study, patients with TTS showed poor connectivity among the brain regions that are important for autonomic functions, including the limbic system.⁶⁸ Recently, a rare case of midventricular TTS (Figures 1A and B) was associated with autoimmune limbic encephalitis.⁶⁵ Before the onset of TTS, the patient exhibited amnesia and topographical disorientation. Brain MRI revealed hyperintense lesions in the bilateral temporal regions, which were most visible during the fluid-attenuated inversion recovery sequence (Figure 1C). Given these findings, it is possible that exaggerated sympathetic stimulation is caused by the limbic system dysfunction resulting from autoimmune limbic encephalitis.

Figure 1 TTS following autoimmune limbic encephalitis. (A and B) Left ventriculographic findings. The diastole (A) and systole (B) images are shown. (C and D) MRI findings. The initial MRI (C) revealed abnormal hyperintense areas (arrows) in the bilateral medial temporal lobes on the fluid-attenuated inversion recovery image (left). Diffusion-weighted imaging (middle) and an apparent diffusion coefficient map (right) both revealed abnormal hyperintensity in these areas. The abnormalities were all resolved in follow-up MRI (D). Abbreviation: MRI, magnetic resonance imaging. Notes: Reproduced from Kakinuma Y, Kimura T, Sakae Y, Kubota S, Ono K, Kinno R. Takotsubo syndrome associated with autoimmune limbic encephalitis: a case report. BMC Cardiovasc Disord. 2021;21(1):86. Creative Commons license and disclaimer available from: http://creativecommons.org/licenses/by/4.0/legalcode.65.

The relationship between the occurrence of TTS and exaggerated sympathetic stimulation remains unclear; however, the spillover of stress-related neuropeptides may be associated with this relationship.⁶⁹ A complex interaction between neocortical regions and the limbic system occurs in response to stress by activating brainstem noradrenergic neurons and stress-related neuropeptides (ie, the neuropeptide Y [NPY] produced by the arcuate nucleus in the hypothalamus). These neuropeptides are stocked in the presynaptic terminals of the postganglionic sympathetic system. When they spill at the myocardium through both microvascular dysfunction and/or direct catecholamine toxicity, myocardial stunning could occur. Patients with TTS due to CNS disease showed worse outcomes than those with TTS due to an emotional trigger.^70,71 Thus, clarifying the role of limbic system diseases in TTS is clinically important. Further work is needed to confirm the link between the pathophysiology of TTS and the brain–heart axis.

Recommended Neurological Approach for TTS

As mentioned above, neurological disorders are clearly associated with TTS. Hence, the following neurological approaches are recommended for patients with TTS.¹⁸ First, every patient with ACS symptoms and an acute neurological disorder, such as subarachnoid hemorrhage, seizure, or ischemic stroke, should be thoroughly evaluated for TTS. The presence of acute stroke symptoms, including face drooping, arm weakness, and speech difficulty, should be checked in all patients with TTS (Table 1). Echocardiography should be routinely performed in cases with any of the following conditions: cardiac symptoms that developed after a CNS event, the presence of ECG dynamics, elevation of CK or troponin, or an MI-like appearance. Second, blood MI parameters should be determined in all patients with CNS disease accompanied by cardiac symptoms, and a routine ECG should be considered regardless of the presence or absence of cardiac symptoms. CNS-triggered TTS must be recognized because appropriate treatment can improve the overall outcome of these patients. The underlying neurological disorder may also improve with adequate TTS treatment. In the chronic phase, all patients should be checked for their memory functions, as memory deficit is often overlooked in the acute phase and is possible sign of limbic encephalitis. If the patients have memory deficits, a neurologist should be consulted.

Moreover, appropriate treatment for neurological disorders may contribute to the management of TTS recurrence. For example, a patient with TTS and autoimmune limbic encephalitis was intravenously injected with methylprednisolone (1 g/day) for 5 days; subsequently, neurological symptoms, such as disorientation, and abnormal MRI findings gradually improved (2 months after admission; Figure 1D).⁶⁵ The more CNS disorders that carry the potential to trigger TTS are detected, the more attention will be drawn to CNS-triggered TTS. TTS must be recognized and understood by neurologists not only to distinguish it from MI, but also to contribute to the positive outcome of these patients.

Optimizing Care with a Psychiatric Approach

One of the well-known triggers of TTS is emotional stress, such as the unanticipated death of a close relative. TTS can also be triggered by positive emotional experiences (for example, a positive job interview, a surprise farewell celebration, or becoming a grandmother); thus, it is also known as the “happy heart syndrome.”⁷² Patients with TTS have a higher rate of psychiatric and neurological disorders than those with ACS.¹⁶ These associations have been extensively reported. Preexisting psychiatric illness and even acute exacerbations of psychiatric disorders or changes in psychotropic medications have been reported as triggers of TTS.⁷³

Psychiatric Association of TTS

Psychiatric comorbidities, such as depression and anxiety, are more prevalent in TTS patients than those with ACS.⁷⁴ Studies have found a link between TTS and anxiety disorders, mood disorders, adjustment disorders, the schizophrenia-spectrum, and neurocognitive and other psychotic disorders.^2,73,75,76 Acute exacerbations of psychiatric disorders, such as anxiety disorders, depression, mania, or psychosis, have been reported as potential triggers of TTS.^75,77 In the International Takotsubo Registry, approximately 10% of patients had acute psychiatric disorders, with mood and anxiety disorders accounting for 4% and 1%, respectively.² Changes in psychiatric medications can also trigger TTS; according to multiple reports, cases have been linked to both the up-titration and overdose of serotonin-norepinephrine reuptake inhibitors.^78–80 Lithium, used in patients with bipolar disorder, has been associated with elevated serum catecholamine levels and reported to trigger TTS.⁸¹ Electroconvulsive therapy, used in patients with severe major depression or bipolar disorder, temporarily and abruptly raises serum catecholamine levels, and is linked to the occurrence of TTS.⁸² In consideration of all these findings, TTS is clearly linked to psychiatric disorders.

Recommended Psychiatric Approach for TTS

Patients with preexisting psychiatric illness have a higher risk of TTS recurrence,⁸³ although the etiology is unknown. In addition, not only psychiatric disorders themselves but also the psychiatric medications used to treat them can be the trigger for TTS. Therefore, it is recommended that patients with TTS should be followed closely for the psychiatric symptoms (Table 1). First, if patients have a preexisting psychiatric illness and/or take psychiatric medication, the type and amount of drug should be determined, and if necessary, the psychiatrist should be consulted even in the acute phase. Second, if emotional stress is not apparent before the onset of TTS, a preexisting psychiatric illness should be considered, whether or not there is a history of one. Finally, TTS patients with psychiatric symptoms should have appropriate long-term management for psychiatric illness after recovering from their cardiac symptoms. Currently, there is little evidence of a benefit of psychiatric treatment in patients with TTS; however, psychiatric illness is also associated with increased mortality. Considering the clear association between TTS and psychiatric disorders, appropriate psychiatric medication may mitigate TTS recurrence.

Optimizing Care with an Oncological Approach

Patients with TTS have a high rate of malignancy.⁸⁴ Desai et al demonstrated that the mean incidence of TTS is 53.0 per 100,000 hospitalized chemotherapy patients with no apparent sex differences.⁸⁵ A recent study demonstrated clear associations between the worse outcome of TTS and cancer disease others than pheochromocytoma.⁵ Patients with cancer have not only physical but also emotional stress; both types of stress would be associated with the occurrence of TTS, as discussed above.⁸⁶ Such patients are likely to experience multiple episodes of stress in relation to the initial diagnosis, the chronic inflammation of the tumor, and the various cancer treatments including chemotherapy and radiation therapy. In addition, the circulation of paraneoplastic mediators may modify the adrenoreceptors in cardiac tissue, leading to systolic dysfunction of LV. All these factors would affect the occurrence of TTS for tumor patients.

Effects of Chemotherapy on TTS

Not only the effects of the tumor itself but also the physical and psychological effects of the associated chemotherapy constitute possible risk factors for TTS. The associations between several types of chemotherapy and TTS have been reported previously.⁸⁷ 5-Fluorouracil (5-FU) is commonly used in many cancers and can induce several side effects, including leukoencephalopathy,⁸⁸ diarrhea, and gastrointestinal mucositis.⁸⁹ 5-FU-induced TTS has been reported in the literature.⁹⁰ Capecitabine,⁹¹ bevacizumab,⁹² combretastatin,⁹³ rituximab,⁹⁴ and tyrosine kinase inhibitors⁹⁵ have also been reported as possible triggers of TTS. Immune checkpoint inhibitors including ipilimumab, pembrolizumab and nivolumab have come to be used for cancer treatments over the last ten years. There has also been a single case report of a patient with metastatic melanoma who showed a TTS-like syndrome with apical ballooning and hyperdynamic basal segment followed by the ipilimumab treatment.⁹⁶ In all cases, the causality between chemotherapy and the occurrence of TTS remains unclear. Studies will be needed.

Recommended Oncological Approach for TTS

The effect of cancer treatment on the occurrence and clinical course of TTS remains unclear. However, considering the clear associations between TTS and cancer revealed in the previous studies,^5,86 tumor screening should be performed for patients with TTS-like syndromes with apical ballooning, especially patients with no apparent neurological or psychiatric disorders (Table 1). On the other hand, patients who underwent chemotherapy for cancer should be followed closely for the presence of cardiac symptoms such as chest pain or breathing difficulty. Cardiac examinations including assays for biomarkers and imaging by ECG and echocardiogram would be helpful for immediate diagnosis of TTS. Chemotherapy can cause neurological disorders such as stroke or encephalopathy,⁸⁸ which may be related to TTS. In addition, a psychological approach is also important for the management of psychiatric stress. Therefore, a multi-pronged approach including cardiac, neurological, psychological, and/or oncological methods is needed for the optimized care of these patients.

Optimizing Care with Other Approaches

Several conditions are associated with TTS occurrence. According to a previous systematic review,³⁵ COPD, asthma, and a pulmonary circulatory disorder have been reported as comorbidities of TTS. Hyper- or hypothyroidism is another comorbidity. A recent study demonstrates that 7% of patients with TTS is related to acute pulmonary disease, and the presence of acute pulmonary disease is associated with a severe in-hospital course and a worse long-term outcome.⁹⁷ Small numbers of TTS patients have a history of alcohol abuse, drug abuse, or surgery. Chronic connective tissue disease, chronic liver disease, and chronic kidney disease have also been found in TTS cases. TTS may be triggered not only by severe medical conditions but also by physiological processes, such as sexual intercourse⁹⁸ and pregnancy.⁹⁹ Surprisingly, acute coronary artery obstruction can also cause TTS.¹⁰⁰ Hence, the medical history of patients should be thoroughly examined. Any remarkable signs should be followed closely, and if necessary, specialists should be consulted in the chronic phase.

Presently, of course, the world is in the throes of a great pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and associated novel coronavirus disease 2019 (COVID-19). SARS-CoV-2 infection has been linked to a number of cardiovascular complications, including arrhythmia, myocarditis, myocardial injury, and exacerbation of chronic cardiac diseases such as heart failure.^101–103 A recent study of 118 patients with COVID-19 who had clinically indicated transthoracic echocardiogram (TTE) found that 5 of them were compatible with a TTS diagnosis.¹⁰⁴ Thus, TTS should be considered in the differential diagnosis of COVID-19 patients with cardiovascular complications, although the diagnosis is difficult because cardiac imaging modalities need to be modified to minimize patient contact.¹⁰⁵ Considering the severity of COVID-19, it is better that these patients are diagnosed in the acute phase. Thus, in patients with COVID-19 with cardiovascular complications, TTE evaluation may be useful to guide treatment and determine the need for further invasive workup.

Conclusion

Although TTS is recognized globally, its exact pathophysiological mechanisms remain unclear. TTS is not a benign condition. Neurological, psychiatric, and oncologic disorders, and even COVID-19, have been reported to be associated with TTS occurrence. Limbic system dysfunction may be a key factor in exaggerated sympathetic stimulation, which results in TTS. Therefore, a multidisciplinary approach, which includes cardiac, neurological, psychiatric, and oncological components, can be beneficial in managing TTS. Further research into the exact pathophysiology is required to improve therapeutic strategies for TTS.