Clinical features of patients with stress-induced cardiomyopathy associated with renal dysfunction: 7 case series in single center
© Shin et al.; licensee BioMed Central Ltd. 2013
Received: 3 January 2013
Accepted: 4 October 2013
Published: 7 October 2013
Stress-induced cardiomyopathy (sCMP) is characterized by transient wall-motion abnormalities involving the left ventricular apex and mid-ventricle that are precipitated by emotional or physical stress. As the heart and kidney influence each other’s function through bidirectional pathways, sCMP can induce renal dysfunction or be induced by renal dysfunction. This study reviewed the clinical characteristics and outcomes of patients with confirmed sCMP associated with renal dysfunction.
We conducted a retrospective analysis of the medical records of all patients from our institution who were diagnosed with sCMP from March 2010 to April 2012. Each patient’s demographic characteristics, presenting symptoms, triggering events, electrocardiographic characteristics, laboratory data, echocardiographic study findings, cardiac catheterization data, and outcomes were reviewed.
Among 30 patients who were diagnosed with sCMP, 7 patients had associated renal dysfunction. Three patients were on maintenance hemodialysis (HD) and 4 patients had acute kidney injury (AKI). Their mean ejection fraction was 35.2% at initial echocardiography, and 57.2% at follow-up echocardiography. Pericardial effusion was detected in all HD patients initially; these patients were treated with intensive HD for suspected under-dialysis status. In patients with AKI, the mean peak serum creatinine was 4.17 mg/dL. Two patients were treated with continuous renal replacement therapy. One patient required maintenance HD, and 1 patient died. Two patients had full renal recovery to their baseline renal function at 7 and 14 days.
Patients with renal dysfunction including those with AKI and those undergoing HD can develop sCMP, renal function must be closely monitored in patients with sCMP. Additionally, it should be considered that patients on HD who develop sCMP may be under-dialyzed.
KeywordsStress cardiomyopathy Acute kidney injury Hemodialysis
Stress-induced cardiomyopathy (sCMP)-also known as takotsubo cardiomyopathy, broken heart syndrome, or transient left apical ballooning syndrome-usually presents as transient left ventricular dysfunction. This syndrome mimics an acute coronary syndrome, electrocardiograms (ECG) often reveal ST elevations, T wave inversion, and Q waves. Cardiac enzymes are also elevated but the coronary arteries are essentially normal. To date, there have been more than 1000 reports published on sCMP. It is estimated that sCMP accounts for 2% of all suspected acute coronary syndromes with 90% of the cases being in postmenopausal women. In all, 39%-80% of patients provide a history of a recent severe emotional or physical stressor [1, 2]. Classic takotsubo cardiomyopathy is characterized by transient hypokinesia of the apical portion of the left ventricle with compensatory hyperkinesias of the basal walls, resulting in apical ballooning. Recently, reverse or inverted takotsubo cardiomyopathy has also been identified with the hyperdynamic apex and akinesia of the base of left ventricular wall [3, 4]. It is generally resolved within days to weeks after initial presentation, and the overall prognosis seems to be favorable, although isolated cases of death have been reported.
Cardiorenal syndrome (CRS) is a disorder of the heart and kidney, whereby acute or long-term dysfunction in one of these organs may induce acute or long-term dysfunction of the other. Changes in the renin-angiotensin-aldosterone system, the sympathetic nervous system, an imbalance between nitric oxide and reactive oxygen species, and inflammation are the cardiorenal connectors in the development of CRS . Similar to that observed in CRS, sCMP can induce renal dysfunction or be induced by renal dysfunction. However, there has been only 1 case report of sCMP with acute kidney injury (AKI) . In this report, we reviewed a case series of 7 patients with confirmed sCMP associated with renal dysfunction including prevalent hemodialysis (HD) or acute kidney injury.
We conducted a retrospective analysis of the medical records of all patients from our institution who were diagnosed with sCMP from March 2010 to April 2012. Patients who met the following criteria of sCMP were included: (1) development of typical takotsubo or inverted takotsubo on echocardiography after emotional or physical stress; (2) no evidence of obstructive epicardial coronary artery disease on coronary angiography (CAG); for those patients who could not undergo CAG, follow-up echocardiography showing improvement of left ventricular function was used to demonstrate the absence of coronary artery obstruction; (3) new ECG abnormalities, including ST-segment elevation, T-wave inversion, or arrhythmia and elevation in troponin I. We identified 30 patients with sCMP. Of these, 7 patients had associated renal dysfunction. Three patients were on maintenance HD with anuric state and 4 patients had AKI. AKI was diagnosed according to the RIFLE criteria, which can be used to classify patients with renal dysfunction according to the degree of impairment into “Risk,” “Injury,” “Failure,” “Sustained loss,” and “End-stage renal disease” categories . Each patient’s demographic characteristics, presenting symptoms, triggering events, ECG characteristics, laboratory data, echocardiographic study findings, cardiac catheterization data, and outcomes were reviewed. Three patients (42.8%) were women and the mean age was 65 years (range, 53 to 77 years). The protocol was approved by the institutional review board of Pusan National University Hospital (E-2012059). Informed consent was exempted by the board because of the retrospective nature of the study.
Clinical characteristics of patients with acute kidney injury and stress-induced cardiomyopathy
Renal replacement therapy
DM, HT, AF
Recovery to baseline renal function and no recur of sCMP
In-hospital death from recurrent VT
Maintenance HD and no recur of sCMP
Pyriform sinus cancer
Recovery to baseline renal function and no recur of sCMP
ECG characteristics, laboratory data, echocardiographic studies, cardiac catheterization data of patients with acute kidney injury and stress-induced cardiomyopathy
Echocardiographic abnormality at presentation
Peak troponin I (ng/mL)
EF at follow-up
Baseline SCr (mg/dL)
Peak SCr (mg/dL)
Follow-up SCr (mg/dL)
Time to recovery of SCr (day)
Typical takotsubo, EF = 33%
Inverted takotsubo, EF = 30%
Typical takotsubo, EF = 34%
Typical takotsubo, EF = 48%
In all 4 patients, the mean baseline serum creatinine was 1.02 mg/dL and the mean serum creatinine at the time of initial echocardiography was 3.0 mg/dL. The first patient’s peak serum creatinine level was 3.76 mg/dL. As this patient had unstable blood pressure with inotropic agent use and decreased urine volume (<400 mL/day), continuous renal replacement therapy (CRRT) was initiated, using the mode of continuous venovenous hemodiafiltration. She was treated with CRRT for 96 hours. After the CRRT was discontinued, she entered the polyuric stage and her renal function returned to baseline within approximately 7 days after diagnosed AKI. She exhibited normal renal function and no recurrence of sCMP at the last examination performed in the nephrology department. Therefore, the degree of renal impairment was “Failure,” according to the RIFLE criteria. The second patient had a maximum creatinine level of 3.45 mg/dL with decreased urine volume (urine volume <300 mL/day) and unstable blood pressure with inotropic agent use; therefore, CRRT was initiated. However, he died during the hospital period. His death was attributed to recurrent ventricular tachycardia. The third patient had biopsy-proven ANCA-associated RPGN and received steroid pulse therapy and cyclophosphamide therapy along with conventional hemodialysis. Despite the immunosuppressive regimen, his renal function did not improve, and therefore, maintenance hemodialysis was initiated. He did not exhibit any recurrence of sCMP at his last follow-up examination. The degree of renal impairment was “End-stage renal disease” according to the RIFLE criteria. In the fourth patient, the serum creatinine level reached to 2.19 mg/dL and then decreased to baseline levels after 14 days, with no recurrence of sCMP. The degree of renal impairment according to the RIFLE criteria was “Injury.”
Clinical characteristics of patients under prevalent hemodialysis with stress-induced cardiomyopathy
Renal replacement therapy
ESRD, DM, HT
No recur of sCMP
ESRD, DM, HT
No recur of sCMP
ESRD, DM, HT, AF, Asthma
No recur of sCMP
ECG characteristics, laboratory data, echocardiographic studies, cardiac catheterization data of patients under prevalent hemodialysis with stress-induced cardiomyopathy
Echocardiographic abnormality at presentation
Peak troponin I (ng/mL)
EF at follow-up
Typical takotsubo, Pericardial effusion, EF = 35%
T -wave inversion
Typical takotsubo, Pericardial effusion, EF = 37%
Typical takotsubo, Pericardial effusion, EF = 30%
Discussion and conclusions
The cases described in this study illustrate that sCMP can occur in patients with renal dysfunction, including end-stage renal disease (ESRD) or AKI. Although sCMP was initially described in Japanese patients, there have been several cases reported in other parts of the world. It is characterized by transient hypokinesia of the apical portion of the left ventricle with compensatory hyperkinesia of the basal walls, resulting in apical ballooning that gives the heart the appearance of a Japanese octopus trap or “takotsubo.” This syndrome mimics an acute coronary syndrome as ECG often reveals ST-segment elevations or T-wave inversions in the precordial leads. The levels of cardiac enzymes are elevated, but angiography shows normal coronary arteries or only minor disease inconsistent with the ECG changes. In previous studies, 39%-80% of patients provide a history of a recent severe emotional or physical stressor [1, 2]. Interestingly, the stressor in all of our patients was physical in nature. The exact mechanism and pathophysiology of sCMP is unknown. There have been a number of theories suggested so far, with catecholamine-induced cardiotoxicity being the most widely supported hypothesis . Plasma catecholamine concentrations at the time of onset were increased in patients with sCMP when compared to patients with myocardial infarction . Exogenous administration of catecholamines and pheochromocytoma have been reported to cause typical features of sCMP adding more evidence to this theory [10, 11]. During stressful conditions, the sympathetic nervous system is activated, and this may influence myocardial contraction. In addition, a different distribution of sympathetic nerves in the myocardium may also be associated with the peculiar wall-motion abnormality. It has been known that sympathetic nervous system hyperactivity is observed in patients with ESRD. Activation of the sympathetic nervous system, assessed using plasma norepinephrine levels, is observed in patients with ESRD treated with HD and in those with early ESRD without HD treatment; the plasma norepinephrine levels in these patients is significantly higher than those in blood pressure-matched and body mass index-matched hypertensive patients or healthy normotensive subjects . Inflammation and oxidative stress play an important role in the pathogenesis of microvascular dysfunction [13, 14]. Recent study found raised C-reactive protein and leucocyte levels in correlation with increased norepinephrine concentration in sCMP patients . It has been demonstrated that vitamin E levels, known to act as a chain-breaking antioxidant that prevents the propagation of free radical reactions, are lower in dialysis patients compared to controls, indicating that there is a significant level of oxidative stress in chronic renal patients . In addition, after dialysis, because of the removal of the antioxidants, an imbalance between oxidants and antioxidants occurs, these instability in the balance of oxidants and antioxidants may be the major cause of cellular oxidative damage. Thus, it can be presumed that, given the conditions of sympathetic nervous hyperactivity and imbalance between oxidants and antioxidants in ESRD patients, triggering of stress might induce sCMP more frequently in these patients than in healthy subjects. Further, all 3 of our patients under maintenance hemodialysis were suspected to have an under-dialysis status because of pericardial effusion and uremic encephalopathy. Therefore, we can presume that the under-dialysis status itself may be a triggering factor for sCMP as a stressor, although further studies are needed to confirm these associations.
Various patterns of sCMP have been recently recognized. In the inverted takotusbo pattern, which is a variant of sCMP, the left ventricular wall exhibits akinesia of the base and hyperdynamic apex [17, 18]. This pattern has been known to present at an earlier age compared with other types of sCMP and has been triggered by emotional or physical stress in all patients . This difference in presentation has been attributed to differences in the sympathetic innervations of the heart with the abundance of adrenoreceptors at the apex compared with the base. One of our patients had an inverted takotusbo pattern in initial echocardiography. As mentioned earlier, the most common finding on the admission ECG was ST-segment elevation. In recent study, the classic ECG features included ST elevation (56%), T wave inversion (39%) and pathological Q waves (32%) . Arrhythmia has been reported in 43.5% of cases with ventricular fibrillation, torsade des pointes, ventricular tachycardia and prolonged QTc being the most common and life-threatening arrhythmias occurring in up to 5.7%. New left and right bundle-branch block on the presenting ECG has been reported. The QTc interval on the presenting ECG ranged from a mean of 450 ms to 501 ms . One of our patients had prolonged QTc interval (501 ms), and he died because of recurrent ventricular tachycardia.
Recently, as the clinical spectrum of sCMP became broader and the disease entity was better understood, it was suggested that it is impractical to routinely perform invasive coronary angiography for definitive diagnosis of sCMP. In fact, current criteria for confirming sCMP include invasive coronary angiography, to exclude the possibility of obstructive coronary artery disease or acute plaque rupture. A recent study demonstrated that a combination of typical LV morphologic change of sCMP and noninvasive demonstration of the absence of significant plaque rupture can be possible alternative diagnostic criteria . However, these modified criteria require further evaluation. One of the patients in the present study died during hospitalization; the death was attributed to recurrent ventricular tachycardia. The in-hospital mortality due to sCMP ranges from 0 to 8%. In view of the associated mortality, the overall outcome is better than that of patients with myocardial infarction. Recurrence of this syndrome is rare and infrequent. In the largest series so far, which consisted of 88 patients, a recurrence rate of 2.7% was reported . In our patients, there has been no recurrence after a mean duration of 11 months.
Cardiac diseases are independently associated with deterioration in kidney function and progression of existing kidney diseases . Conversely, both decrease in glomerular filtration rate and proteinuria are independent risk factors for the development of cardiovascular disease . CRS is a disorder of the heart and kidney, whereby acute or long-term dysfunction in 1 of these organs may induce acute or long-term dysfunction of the other. The 2 organs are connected to regulate blood pressure, vascular tone, diuresis, natriuresis, peripheral tissue perfusion and oxygenation. Recently, a new classification of CRS has been developed to reflect the likely primary and secondary pathology and time-frame . Type 1 CRS consists of an abrupt worsening of cardiac function leading to AKI. Proposed pathophysiologic mechanisms include reduced transglomerular pressure, elevated renal interstitial pressure, myogenic and neural reflexes, activation of sympathetic nervous and renin-angiotensin-aldosterone systems, non-osmotic release of arginine vasopressin, local production of endothelin, and enhanced proinflammatory pathways. Type 2 CRS comprises chronic abnormalities in cardiac function causing progressive chronic kidney disease. Accelerated renal cell apoptosis and replacement fibrosis is considered to be the dominant mechanism. Type 3 CRS reflects an abrupt worsening of renal function causing acute cardiac dysfunction. This syndrome is precipitated by salt and water overload, acute uremic myocyte dysfunction, and neurohormonal dysregulation. Type 4 CRS comprises a state of chronic kidney disease that contributes to a decline in cardiac function. Cardiac myocyte dysfunction and fibrosis is believed to be the predominant pathophysiologic mechanism. Type 5 CRS reflects a systemic condition such as sepsis causing both cardiac and renal dysfunction. In this type, the predominant pathophysiological disturbance is microcirculatory dysfunction as a result of acutely abnormal immune cell signaling, catecholamine cellular toxicity, and enzymatic activation which result in simultaneous organ injury often extending beyond both the heart and the kidneys. The use of this classification can help physicians characterize groups of patients and provides the rationale for specific management strategies.
It could be presumed that sCMP and CRS share the comparable mechanism regarding the sympathetic nervous system activation, inflammation and oxidative stress in the pathogenesis of microvascular dysfunction. In our patients, 4 had AKI (injury, failure, and ESRD in 1 each) associated with sCMP. Because the serum creatinine level was already increased at the time that sCMP was diagnosed, we could not appropriately classify the patients according to the CRS classification; instead, we divided them into acute CRS (type 1 or type 3) depending on the clinical course or CRS type 5 regarding the sepsis due to infectious triggering factors.
Two (50%) of the patients with AKI were treated with CRRT to manage the congestive symptoms and correct the abnormalities in electrolyte levels and acid–base status, accompanying hemodynamic instability. In fact, it has been known that the coexistence of heart and kidney failure in the same subject is associated with an extremely bad prognosis . In patients with acute heart failure, an acute increase in serum creatinine level of >0.3 mg/dL is associated with longer hospitalization time, increased mortality, and more frequent re-admissions . Although diuretics have been the mainstay of treatment, they are often unsuccessful in reversing the vicious cycle of volume overload, worsening cardiac function, and azotemia. Renal replacement therapy (RRT) in the form of isolated or continuous ultrafiltration, with or without a component of solute clearance (hemofiltration or hemodialysis), has been increasingly utilized as a therapeutic tool in this setting. A previous study examined the isolated ultrafiltration strategy in 100 patients with hypervolemic congestive heart failure compared with the intravenous diuretics strategy adopted in 100 patients. It demonstrated greater weight loss, decreased need for vasoactive drugs, and fewer rehospitalizations and emergency department visit in the ultrafiltration group, but no difference in mortality . Although the clinical necessity of RRT in cases of life-threatening hyperkalemia or acidemia with AKI is clear, the adjunctive role of RRT (hemofiltration or hemodialysis) in the treatment of acute decompensated heart failure is not obvious. A previous study suggested that because severe hypocalcemia is a potential cause of reversible heart failure and acute or acute on chronic renal dysfunction is often hypocalcemic, correction of hypocalcaemia via continuous venovenous hemofiltration might improve cardiac function in acute decompensated heart failure . However, further research examining the use of RRT in CRS is necessary.
Our current study has some limitations. First, the number of patients is small. Second, significant numbers of patients did not meet the current definition of classic sCMP. As it was not possible to perform invasive coronary angiography in 5 patients, we demonstrated the absence of coronary artery obstruction showing recovery of wall motion abnormality and improvement of left ventricular function to perform follow-up echocardiography. Third, we could not present the exact relevance of sCMP and CRS. Further investigation is necessary to overcome these limitations.
In conclusion, these cases showed that concomitant sCMP can occur in patients with renal dysfunction including ESRD or AKI, especially associated with CRS. Therefore, the renal function of any patient with sCMP should be closely monitored to facilitate the early diagnosis of AKI. ESRD patient who develops sCMP could be considered to be under-dialyzed, but further studies are needed to confirm this.
This work was supported by clinical research grant from Pusan National University Hospital.
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