Key result
Age at diagnosis independently predicts ~6% higher mortality in amiodarone-induced thyrotoxicosis.
Cohort (n=113)
No
Hazard Ratio: 1.06 (95% CI 1.02–1.1)
p-value: p=0.001
Amiodarone-induced thyrotoxicosis is associated with a substantial long-term clinical burden, including high rates of cardiovascular events, hospitalization, and mortality, which are primarily driven by older age at diagnosis rather than thyrotoxicosis type.
Age informs mortality risk stratification in amiodarone-induced thyrotoxicosis; leaves open whether age-targeted interventions improve survival.
Amiodarone-induced thyrotoxicosis is a recognized adverse effect of amiodarone therapy. However, its long-term effects on cardiovascular morbidity, hospitalization, and mortality remain insufficiently characterized. The objective of this study is to evaluate the incidence of cardiovascular events, hospitalizations, and all-cause mortality following amiodarone-induced thyrotoxicosis and to assess their association with clinical, biochemical, and therapeutic parameters. A retrospective cohort study was conducted including 113 adult patients diagnosed with amiodarone-induced thyrotoxicosis and followed at a tertiary endocrinology center between 2008 and 2024. Clinical and biochemical characteristics, therapeutic interventions, cardiovascular events, hospital admissions, and mortality were recorded. The event-free survival was evaluated using Kaplan–Meier curves, and predictors of outcomes were assessed using Cox proportional hazard regression models. Fifty patients (44.2%) were classified as amiodarone-induced thyrotoxicosis type 1 and 63 patients (55.8%) as amiodarone-induced thyrotoxicosis type 2. Over a median follow-up of 52 months, 42.5% experienced at least one cardiovascular event, 38.0% required hospitalization, and 33.6% died. Serum free thyroxine levels at diagnosis were significantly higher in patients who developed cardiovascular events (hazard ratio: 2.6; 95% confidence interval: 1.9–3.7 vs. hazard ratio: 2.3; 95% confidence interval: 1.6–3.4 ng/dL; p=0.042). Kaplan–Meier analysis showed reduced survival in older patients (p<0.001). In the multivariate model, age at diagnosis was the only independent predictor of mortality (hazard ratio=1.06; 95% confidence interval: 1.02–1.10; p=0.001). Neither amiodarone-induced thyrotoxicosis type nor treatment intensity were significantly associated with cardiovascular outcomes, hospitalization, or survival. Amiodarone-induced thyrotoxicosis is associated with substantial long-term clinical burden. In unadjusted analysis, elevated free thyroxine levels were associated with cardiovascular events, although this association did not reach significance after multivariate adjustment. Age at amiodarone-induced thyrotoxicosis diagnosis was the only independent predictor of mortality. Amiodarone-induced thyrotoxicosis type and treatment intensity did not significantly influence outcomes.
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Serrano et al. (2026) conducted a cohort in Amiodarone-induced thyrotoxicosis (n=113). Age at diagnosis was evaluated on all-cause mortality (HR 1.06, 95% CI 1.02-1.10, p=0.001). In patients with amiodarone-induced thyrotoxicosis, age at diagnosis was the only independent predictor of mortality (HR 1.06; 95% CI 1.02-1.10; P=0.001).
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