Abstract
Takotsubo cardiomyopathy (TCM) is a life-threatening transient left ventricular dysfunction triggered by either physical or emotional stressors. Concerns have been raised on reports of TCM after the coronavirus disease 2019 (COVID-19) vaccine. Our study provides comprehensive detail on COVID-19 vaccine-induced TCM.
We conducted a systemic literature search using major databases, including PubMed, EMBASE, and Google Scholar up to November 2023, to identify cases of COVID-19 vaccine-induced TCM using the MeSH terms and keywords "covid-19 vaccines" and "takotsubo cardiomyopathy".
We identified 15 case reports, including 16 patients with COVID-19 vaccine-induced TCM. The mean age was 55.81 ± 19.13 years, and 75% of the patients were female. The most common presentation was chest pain (62.5%), and the average time to first symptom onset was 3.12 ± 2.24 days. COVID-19 vaccine-induced TCM was reported in 43.75% of patients receiving the first and second dose each, and 87% of patients had messenger ribonucleic acid (mRNA) COVID-19 vaccine (Pfizer, Moderna). The elevated level of cardiac troponins was found in all the patients with a left ventricular ejection fraction (LVEF) of <50% in 15 patients, and T-wave inversion (50%) was the most common electrocardiographic finding. The mean length of the hospital stay was 7.27 ± 3.95 days, and 87% of patients were discharged.
COVID-19 vaccine-induced TCM is a rare but life-threatening complication. TCM should be included in the differential diagnosis of chest pain or dyspnea in patients recently receiving the COVID-19 vaccine.
Keywords: broken-heart syndrome, stress induced cardiomyopathy, takotsubo cardiomyopathy (ttc), covid-19 vaccine complication, covid-19 vaccine
Introduction and background
Recently, the global response to the coronavirus disease 2019 (COVID-19) pandemic has been marked by the rapid development and deployment of various vaccines to mitigate the spread and severity of the virus [1]. While the vaccines have demonstrated remarkable efficacy in preventing severe illness and death associated with COVID-19, the scientific and medical communities continually evaluate and monitor potential adverse effects to ensure the safety of vaccination programs [2]. Vaccines developed against COVID-19 include messenger ribonucleic acid (mRNA) vaccines (Pfizer-BioNTech (Mainz, Germany) and Moderna (Massachusetts, United States)), viral vector vaccines (AstraZeneca (Cambridge, United Kingdom), Johnson & Johnson's Janssen (New Jersey, United States), and Sputnik V (The Gamaleya National Center of Epidemiology and Microbiology, Moscow, Russia)), and protein subunit vaccines (Novavax (Maryland, USA)) [3]. Although each vaccine has demonstrated its efficacy in COVID-19 prevention, no vaccine is free from any side effects or complications. Vaccine-induced side effects or complications generally depend on the type of vaccine and the dosing of the vaccine [4]. Commonly reported side effects include injection site redness, swelling, pain, fatigue, headache, nausea, myalgia, or fever (Table 1) [5].
Table 1. Commonly reported side effects of COVID-19 vaccine.
Source: [5]
| Side effect | Number of patients | Percentage (%) |
| Injection site pain | 851 | 78.4 |
| Injection site swelling | 177 | 16.3 |
| Fever | 300 | 27.6 |
| Headache | 359 | 33.1 |
| Myalgia | 408 | 37.6 |
| Fatigue | 563 | 51.8 |
| Nausea | 164 | 15.1 |
COVID-19 vaccine has also been reported to involve any organ system of the body and vaccine-induced cardiovascular, neurological, and gastrointestinal system complications have also been reported [6]. Myocarditis, pericarditis, myocardial infarction, myocardial injury, coagulopathy, heart failure, and arrhythmias are reported cardiovascular complications of COVID-19 vaccine [7]. Takotsubo cardiomyopathy (TCM) is also an uncommon, life-threatening complication of the COVID-19 vaccine, especially with mRNA COVID-19 vaccines (Pfizer-BioNTech and Moderna) [8].
TCM is a sudden, transient heart syndrome that mimics acute coronary syndrome. It is also referred to as broken heart syndrome or stress cardiomyopathy, characterized by left ventricular apical akinesia [9]. This condition typically occurs following intense emotional or physical stress such as the death of a loved one, a traumatic event, or a severe illness [9]. The association between the COVID-19 vaccine and the development of TCM has not been widely reported, and only a limited number of cases have been reported [10]. Our study aims to consolidate and analyze the evidence regarding COVID-19 vaccine-induced TCM.
Review
Material and methods
A systematic and comprehensive literature search was conducted using electronic databases, including PubMed, MEDLINE, Embase, and Cochrane Library, in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) guidelines [11] (Figure 1). Our data search included the Medical Subject Headings (MeSH) terms and keywords for the COVID-19 vaccine and takotsubo cardiomyopathy from the date of inception to November 19, 2023. We did not limit our search to any language or geographical area. Our search also included the references of the relevant articles identifying all the pertinent studies, and all citations were downloaded to EndNote version 12.0 (https://endnote.com/downloads/available-updates/) for further screening and extraction of related data. We stratified only those studies reporting COVID-19 vaccine-inducing TCM regardless of the type and dosing. All those studies with a lack of COVID-19-induced TCM data were excluded.
Figure 1. PRISMA flow diagram.
PRISMA: Preferred Reporting Items for Systematic Review and Meta-Analyses
Our initial search revealed 3721 articles; two authors screened titles and abstracts of identified articles based on inclusion and exclusion criteria. Full-text articles of potentially relevant studies were then assessed for eligibility. All included studies were evaluated independently by two authors using the critical appraisal tool of the Joanna Briggs Institute for case reports. A pre-defined Microsoft Excel data sheet (Microsoft Corporation, Redmond, WA) was used to extract data. Relevant data were extracted from eligible studies, including study design, participant demographics, type of COVID-19 vaccine administered, time to onset of takotsubo cardiomyopathy, dose of the vaccine, length of hospital stay, electrocardiographic (ECG) changes, ejection fraction (%), treatment, and clinical outcomes. We expressed the categorical data as proportions (%) and the numerical data as mean and standard deviation (SD) using the Statistical Package for the Social Sciences (SPSS) 24.0 (IBM Corp., Redmond, WA). Data extraction was performed independently by two reviewers, with discrepancies resolved through consensus. The quality of the systematic review was assessed using the A Measurement Tool to Assess Systematic Reviews 2 (AMSTAR 2) tool [12].
Results
Out of 3721 articles, 31 studies were assessed for eligibility, and 15 case reports were included in our study, reporting 16 patients developing TCM following the COVID-19 vaccine. Characteristics of each study, including demographics, type of the vaccine, dosage of the vaccine, onset of symptoms following vaccination, manifestation of TCM at presentation, electrocardiographic changes, ejection fraction, length of the hospital stay, and the management and outcome of each patient are shown in Table 2 [8,10,13-25].
Table 2. Characteristics of reported cases of COVID-19 vaccine-induced TCM.
TCM: takotsubo cardiomyopathy, LVEF: left ventricular ejection fraction, M: male, NR: not reported, F: female, ECG: electrocardiography, mRNA: messenger ribonucleic acid
| Author/Year | Age (years)/Sex | Type of vaccine | Dose of vaccine | Days to symptom onset (days) | Symptoms | Troponin level | LVEF (%) | ECG | Hospital stays (day) | Management | Outcome |
| Reza et al., 2023 [8] | 59/F | mRNA-1273 | 3rd | 3 | Dyspnea | Elevated | < 50 | Abnormal | 7 | Furosemide, hydrocortisone, norepinephrine | Improved |
| Minicullo et al., 2023 [10] | 54/F | BNT162b2 | 1st | 1 | Dyspnea, confusion | Normal | < 50 | Abnormal | 4 | Oxygen, steroids, diuretics | Improved |
| Beshai et al., 2022 [13] | 45/M | mRNA-1273 | 2nd | 3 | Chest discomfort | Elevated | < 50 | Abnormal | 4 | NA | Improved |
| Chen et al., 2023 [14] | 67/F | mRNA-1273 | 1st | 7 | Palpitation, chest discomfort | Elevated | < 50 | Abnormal | 7 | Bisoprolol, steroids, diuretics | Improved |
| Yamaura et al., 2022 [15] | 30/F | BNT162b2 | 2nd | 2 | Cold sweat, chest discomfort | Elevated | < 50 | Abnormal | 15 | The patient was managed without medical therapies | Improved |
| Tedeschi et al., 2022 [16] | 71/F | BNT162b2 | 1st | 1 | Dyspnea, chest discomfort | Elevated | < 50 | Abnormal | NR | NR | Improved |
| Gill et al., 2022 [17] | 18/M | BNT162b2 | 2nd | 3 | Asymptomatic | Elevated | < 50 | Abnormal | 3 | NR | Death |
| Gill et al., 2022 [17] | 18/M | BNT162b2 | 2nd | 4 | Asymptomatic | Elevated | < 50 | Abnormal | 4 | NR | Death |
| Boscolo et al., 2021 [18] | 63/F | mRNA-1273 | 1st | 1 | Dyspnea, fever | Elevated | < 50 | Abnormal | NR | NR | Improved |
| Jani et al., 2021 [19] | 65/F | mRNA-1273 | 1st | 1 | Headache, nausea, muscle ache, chest discomfort | Elevated | < 50 | Abnormal | NR | Dual antiplatelet, metoprolol succinate, | Improved |
| Toida et al., 2021 [20] | 80/F | BNT162b2 | 1st | 1 | Anorexia, generalized fatigue | Elevated | < 50 | Abnormal | 13 | Intravenous fluid, oxygen therapy | Improved |
| Stewart et al., 2021 [21] | 50/F | ChadOX1 nCOV-19 | 2nd | 7 | Nausea, chest discomfort | Elevated | < 50 | Abnormal | 5 | Oxygen therapy, dual antiplatelet | Improved |
| Fearon et al., 2021 [22] | 73/F | mRNA-1273 | NR | 1 | Nausea, chest discomfort, dyspnea | Elevated | > 50 | Abnormal | 8 | Diuretics, antiplatelet therapy, metoprolol | Improved |
| Wardhere et al., 2021 [23] | 68/F | mRNA-1273 | 2nd | 7 | Chest discomfort | Elevated | < 50 | Abnormal | NR | NR | Improved |
| Crane et al., 2021 [24] | 72/M | ChadOX1 nCOV-19 | 1st | 4 | Chest pain, fatigue, myalgias, fever | Elevated | < 50 | Abnormal | 10 | Dual antiplatelet therapy, losartan, metoprolol | Improved |
| Vidula et al., 2021 [25] | 60/F | BNT162b2 | 2nd | 4 | Chest pain, nausea | Elevated | < 50 | Abnormal | NA | metoprolol succinate, lisinopril | Improved |
Sixteen (75%) patients were female, and four (25%) patients were male, with a median age of 61.5 years (mean ± SD: 55.81 ± 19.13), and the median number of days to onset of the first symptom was 3 (mean ± SD: 3.12 ± 2.24). Length of hospital stay was not reported in five patients, and the mean length of hospital stay among 67% of patients was 7.27 ± 3.95 (Table 3).
Table 3. Demographics of patients included in the study.
SD: standard deviation
| Variable | Mean | SD |
| Age (years) | 55.81 | 19.13 |
| Days to first symptom onset | 3.12 | 2.24 |
| Length of hospital stay (days) | 7.27 | 3.95 |
Among the COVID-19 vaccine types, 87.5% of the patients received mRNA COVID-19 vaccine, and 13% received a viral vector vaccine (Table 4). Regarding COVID-19 vaccine dose-induced TCM, 43.5% of patients reported TCM with the first dose regardless of the type of vaccine (Table 5). Chest pain was the most underlined manifestation (62.5%) in individuals with COVID-19-induced TCM, followed by dyspnea (31.25%), nausea (18.75%), and atypical symptoms (25%). Two patients reported no symptoms (Table 6).
Table 4. Types of COVID-19 vaccines and their percentage.
| Vaccine type | Number of patients | Percentage (%) |
| Pfizer-BioNTech | 8 | 50 |
| Moderna | 6 | 37.5 |
| ChAdOx1 nCoV-19 | 2 | 12.5 |
Table 5. Dosage of COVID-19 vaccine inducing TCM.
TCM: takotsubo cardiomyopathy
| Dose of COVID-19 vaccine | Number of patients | Percentage (%) |
| 1st | 7 | 43.75 |
| 2nd | 7 | 43.75 |
| 3rd | 1 | 6.26 |
| No dose reported | 1 | 6.26 |
Table 6. Clinical manifestation of patients presented with COVID-19 vaccine-induced TCM.
TCM: takotsubo cardiomyopathy
| Clinical symptomology | Number of patients | Percentage (%) |
| Chest pain | 10 | 62.5 |
| Dyspnea | 5 | 31.25 |
| Nausea | 3 | 18.75 |
| Atypical | 4 | 25 |
All patients were found to have elevated cardiac troponin with abnormal ECG findings and abnormal LVEF on echocardiography (Table 7). Fourteen (87.5%) patients showed successful recovery and were discharged, and 12.5% of the patients died.
Table 7. Cardiovascular parameters of the patients presented with TCM.
ECG: electrocardiography; TCM: takotsubo cardiomyopathy
| Variable | Number of patients | Percentage (%) | |
| Cardiac troponin | Elevated | 16 | 100 |
| normal | 0 | 0 | |
| ECG findings | ST-segment changes | 5 | 31.25 |
| T-wave changes | 8 | 50 | |
| Prolonged QTc interval | 3 | 18-75 | |
| Ejection fraction (%) | < 50 | 15 | 92 |
| > 50 | 1 | 6.25 | |
| Outcome | Discharge | 14 | 87.5 |
| Died | 2 | 12.5 |
Discussion
The study's demographic profile reveals that most patients (75%) were female, with a median age of 61.5 years. This distribution aligns with the general epidemiology of TCM, which predominantly affects postmenopausal women. The mean time to symptom onset following COVID-19 vaccination was 3.12 days, emphasizing the acute nature of the cardiac complications [13]. Chest pain emerged as the predominant symptom, reported in 62.5% of patients. This aligns with the typical presentation of TCM, where acute emotional or physical stressors trigger severe chest pain, mimicking symptoms of myocardial infarction [15]. Additionally, dyspnea, nausea, and atypical symptoms were also observed, highlighting the diverse clinical spectrum of TCM [17].
The analysis of the included cases indicates that TCM occurred after both the first and second doses of COVID-19 vaccines, with 43.75% of patients experiencing TCM following each dose. Examining the dosing of COVID-19 vaccines in the context of TCM, it is noteworthy that 43.75% of patients experienced TCM after the first dose, irrespective of the vaccine type. This finding challenges the assumption that TCM might be associated solely with the second dose, as observed in some vaccine-related adverse events [26]. Jani et al. reported that COVID-19 vaccine-induced TCM had been reported after administration of the first or second dose [20]. Similarly, a 30-year-old female presented with sudden-onset dyspnea and chest pain following the second dose of the COVID-19 vaccine and was diagnosed with TCM [15]. This temporal association with vaccination provides the potential link between the immune response triggered by the vaccine and the development of TCM, which needs to be further studied.
Our study reveals that the majority (87.5%) of patients who developed TCM received mRNA COVID-19 vaccines, specifically Pfizer-BioNTech and Moderna. This observation raises intriguing questions about potential mechanisms specific to mRNA vaccines that might contribute to the development of TCM [27]. The exact mechanisms linking mRNA vaccines to TCM remain elusive and warrant further investigation. The study's outcomes shed light on the severity and recovery of patients who developed TCM post-vaccination. Among the cohort, 87.5% of patients were discharged following successful recovery, emphasizing the transient and reversible nature of TCM. However, 12.5% of patients developed the complication, underscoring the potentially life-threatening nature of this vaccine-related adverse event.
The specific mechanisms underlying vaccine-induced TCM remain unclear. It has been proposed that certain changes in ischemia-induced myocardium may induce TCM triggered by certain potential factors, including microvessel dysfunction, coronary artery vasospasm, and direct myocardial injury due to surge currents [28,29]. This phenomenon is triggered by the excessive release of catecholamines, including epinephrine or norepinephrine, through marked activation of the sympathetic nervous system (SNS), which may involve the hypothalamic-pituitary-adrenal axis [30]. Impaired neural networks in the limbic region may also be impaired during stress in patients with TCM [30]. A rat model of TCM suggests that epinephrine affinity switching from beta-2-adrenoceptors-Gs to Gi protects the myocardium from toxicity during stress [31]. Studies have reported elevated cytokine levels and inflammatory myocardial macrophage infiltration in TCM patients. Endothelial dysfunction in TCM patients is also a documented phenomenon [32]. Similarly, another potential mechanism involves the free-floating spike protein interaction with angiotensin-converting enzyme-2 (ACE-2) receptors, leading to an imbalance between angiotensin II and angiotensin, possibly leading to an acute elevation in blood pressure and myocardial stress following vaccination [33]. Acute emotional or physical stress may induce massive release of cortisol and catecholamines, stimulating various pathways, including coronary artery spasm, direct myocardial cell injury, and microvascular dysfunction [34].
Ongoing surveillance and reporting of vaccine-related adverse events, including TCM, are crucial for refining risk-benefit assessments and optimizing vaccination strategies. Establishing standardized diagnostic criteria and management guidelines for vaccine-induced TCM is imperative to ensure timely and effective interventions [14]. Future research should focus on elucidating the specific mechanisms linking COVID-19 vaccination, especially mRNA vaccines, to the development of TCM. Large-scale epidemiological studies, genetic analyses, and in-depth exploration of the immune response post-vaccination are essential to unravel the complexities of this rare adverse event [27].
Despite its valuable insights, the study has limitations that must be acknowledged. The small sample size of 16 patients from 15 case reports limits the generalizability of findings. Additionally, reporting biases and the potential for underreporting or selective reporting of cases may impact the overall interpretation of the results. The absence of a control group further limits the ability to establish a direct causal relationship between COVID-19 vaccination and TCM. Moreover, we do not have any data on the patients regarding previous history of COVID-19 infection or ischemic heart disease.
Conclusions
This review contributes valuable insights into the rare but severe complication of TCM following COVID-19 vaccination and has significant clinical implications. The study emphasizes the need for continued surveillance, in-depth research, and standardized reporting of vaccine-related adverse events. Clinicians should remain vigilant, considering TCM in the differential diagnosis of patients presenting with chest pain or dyspnea post-vaccination, especially in the context of mRNA vaccines. As the global community strives to balance the benefits and risks of vaccination, ongoing research is essential to refine guidelines and optimize the safety profile of COVID-19 vaccines.
The authors have declared that no competing interests exist.
Author Contributions
Concept and design: Hira Nasir, Nikita Kumari, Bai Manita, Binayak Singh, Siddhi Shah, Joti Devi, Rezaur Rahman Reza, Utsav Patel
Drafting of the manuscript: Hira Nasir, Nikita Kumari, Bai Manita, FNU Suman , Binayak Singh, Siddhi Shah, Rezaur Rahman Reza, Khalid H. Mohamed, Saria M. Mokhtar, Utsav Patel
Supervision: Hira Nasir, Nikita Kumari, Bai Manita, FNU Suman , Binayak Singh, Siddhi Shah, Sarfaraz Ahmad
Acquisition, analysis, or interpretation of data: Bai Manita, FNU Suman , Binayak Singh, Saher T. Shiza, Iqra Samreen, Joti Devi, Khalid H. Mohamed, Sarfaraz Ahmad, Saria M. Mokhtar
Critical review of the manuscript for important intellectual content: Bai Manita, Binayak Singh, Saher T. Shiza, Iqra Samreen, Joti Devi, Khalid H. Mohamed, Sarfaraz Ahmad
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