Key result
Chemotherapy-induced takotsubo syndrome accounts for 1-2% of TS triggers, predominantly affects women (60-70%), and is associated with substantial mortality.
Why the study?
What are the clinical features and outcomes of patients with chemotherapy-induced takotsubo syndrome?
What are the clinical features and outcomes of patients with chemotherapy-induced takotsubo syndrome?
Chemotherapy-induced takotsubo syndrome has a distinct demographic profile compared to overall TS and is associated with substantial mortality, though limited data suggest chemotherapy can be safely reinitiated.
Chemotherapy treatment of malignancy accounts for 1–2% of takotsubo syndrome (TS) triggers. Women comprise 60–70% of patients with chemotherapy-associated TS, a distinctly lower prevalence than the 90% female prevalence in TS overall. Fluorouracil is the most commonly reported TS-triggering chemotherapeutic agent, although this must be interpreted in the context of the frequency of worldwide use of this agent. The onset of TS relative to chemotherapy initiation is quite variable, ranging from the initial administration to subsequent chemotherapy cycles several weeks beyond initiation. Limited information suggests chemotherapy can be safely reinitiated once the patient has recovered from the initial TS event. Having a TS event in the setting of chemotherapy treatment for malignancy is associated with substantial mortality.
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Storey et al. (2020) conducted a review in Chemotherapy-induced Takotsubo Syndrome. Chemotherapy was evaluated. Chemotherapy-induced takotsubo syndrome accounts for 1-2% of TS triggers, predominantly affects women (60-70%), and is associated with substantial mortality.
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