A systemic immune-inflammation index cutoff of 645.16 predicted successful pharmacological cardioversion in new-onset AF with 75% sensitivity and 75% specificity (AUC 0.803; 95% CI 0.710-0.895).
Observational (n=95)
Does the systemic immune-inflammation index (SII) predict successful pharmacological cardioversion with intravenous amiodarone in patients with new-onset atrial fibrillation?
The systemic immune-inflammation index (SII) is a strong independent predictor of successful pharmacological cardioversion with amiodarone in patients with new-onset atrial fibrillation.
Effect estimate: AUC 0.803 (95% CI 0.710-0.895)
p-value: p=<0.001
Background: Pharmacological cardioversion (PC) with antiarrhythmic agents is a common initial rhythm control strategy in patients with new-onset atrial fibrillation (AF). However, predictive tools for estimating the likelihood of successful PC remain limited. The systemic immune-inflammation index (SII), a novel composite marker derived from neutrophil, lymphocyte, and platelet counts, may reflect atrial inflammatory burden and structural remodeling. This study aimed to investigate the prognostic value of SII in predicting pharmacological cardioversion success in patients with acute-onset symptomatic AF. Methods: This prospective observational study included patients with hemodynamically stable, new-onset symptomatic AF admitted since October 2025. All patients received intravenous amiodarone for pharmacological cardioversion. Baseline clinical, echocardiographic, and laboratory parameters were recorded. Patients were classified into cardioversion-success and non-response groups based on ECG-confirmed restoration of sinus rhythm. Logistic regression analyses were performed to identify independent predictors of rhythm control, and ROC curves were generated to determine predictive performance. Results: Among 95 patients (mean age 54.2 ± 9.8 years, 48.4% female), successful pharmacological cardioversion was achieved in 74.7%. Compared to the non-response group, the cardioversion-success group had significantly lower SII levels (p < 0.001) and left atrial volume index (LAVI, p < 0.001). Multivariate analysis identified both SII and LAVI as independent predictors of cardioversion success. Inverse correlations were observed between both SII (r = −0.419, p < 0.01) and LAVI (r = −0.567, p < 0.01) and rhythm control. The optimal SII cutoff of 645.16 predicted successful rhythm restoration with 75% sensitivity and 75% specificity (AUC: 0.803, 95% CI: 0.710–0.895). Conclusions: Higher SII levels were independently associated with lower rates of successful pharmacological cardioversion in patients with new-onset atrial fibrillation. Incorporating SII into routine assessment may enhance clinical decision-making and patient stratification for rhythm control strategies.
Mirzaoğlu et al. (2026) conducted an observational in new-onset atrial fibrillation (n=95). Systemic immune-inflammation index (SII) was evaluated on Successful pharmacological cardioversion (AUC 0.803, 95% CI 0.710-0.895, p=<0.001). A systemic immune-inflammation index cutoff of 645.16 predicted successful pharmacological cardioversion in new-onset AF with 75% sensitivity and 75% specificity (AUC 0.803; 95% CI 0.710-0.895).