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Abstract Aims Takotsubo syndrome (TS) is a heart condition mimicking acute myocardial infarction. TS is characterized by a sudden weakening of the heart muscle, usually triggered by physical or emotional stress. In this study, we aimed to investigate the effect of pharmacological interventions on short‐ and long‐term mortality in patients with TS. Methods and results We analysed data from the SWEDEHEART (the Swedish Web System for Enhancement and Development of Evidence‐based care in Heart disease Evaluated According to Recommended Therapies) registry, which included patients who underwent coronary angiography between 2009 and 2016. In total, we identified 1724 patients with TS among 228 263 individuals in the registry. The average age was 66 ± 14 years, and 77% were female. Nearly half of the TS patients (49.4%) presented with non‐ST‐elevation acute coronary syndrome, and a quarter (25.9%) presented with ST‐elevation myocardial infarction. Most patients (79.1%) had non‐obstructive coronary artery disease on angiography, while 11.7% had a single‐vessel disease and 9.2% had a multivessel disease. All patients received at least one pharmacological intervention; most of them used beta‐blockers (77.8% orally and 8.3% intravenously) or antiplatelet agents aspirin (66.7%) and P2Y 12 inhibitors (43.6%). According to the Kaplan–Meier estimator, the probability of all‐cause mortality was 2.5% after 30 days and 16.6% after 6 years. The median follow‐up time was 877 days. Intravenous use of inotropes and diuretics was associated with increased 30 day mortality in TS hazard ratio (HR) = 9.92 ( P < 0.001) and HR = 3.22 ( P = 0.001), respectively, while angiotensin‐converting enzyme inhibitors and statins were associated with decreased long‐term mortality HR = 0.60 ( P = 0.025) and HR = 0.62 ( P = 0.040), respectively. Unfractionated and low‐molecular‐weight heparins were associated with reduced 30 day mortality HR = 0.63 ( P = 0.01). Angiotensin receptor blockers, oral anticoagulants, P2Y 12 antagonists, aspirin, and beta‐blockers did not statistically correlate with mortality. Conclusions Our findings suggest that some medications commonly used to treat TS are associated with higher mortality, while others have lower mortality. These results could inform clinical decision‐making and improve patient outcomes in TS. Further research is warranted to validate these findings and to identify optimal pharmacological interventions for patients with TS.
Pétursson et al. (Thu,) studied this question.