Validation of 2 Syncope Risk Scores and Comparison With Physician Risk Estimation

Importance: Risk stratification is a key component of syncope management in the emergency department (ED), but objective risk-stratification tools have not been widely adopted. Objective: To externally validate 2 risk-stratification tools, the Canadian Syncope Risk Score (CSRS) and FAINT score, and compare their performance with unstructured physician-estimated risk. Design, Setting, and Participants: This prospective, observational, multicenter cohort study was conducted across the US from September 2020 to September 2024, enrolling ED patients aged 40 years or older with syncope or presyncope and no serious diagnosis during initial evaluation. Data were analyzed from September to December 2025. Exposure: Presence of syncope or presyncope. Main Outcomes and Measures: The primary outcome was a serious adverse outcome within 30 days of the ED visit. This included both cardiac and noncardiac outcomes for the CSRS and exclusively cardiac outcomes for the FAINT score. Unstructured estimates of each patient's risk for serious adverse outcome were obtained from the treating attending physician. Risk scores and physician-estimated risk were assessed using the area under the receiver operating characteristic curve (AUROC). Sensitivity and negative predictive value (NPV) were also calculated. Results: A total of 1263 patients were analyzed (median [IQR] age, 66.0 [55.0-74.0] years; 676 female [53.5%]), of whom 74 (5.9%) had a serious adverse outcome and 62 (4.9%) had a serious cardiac outcome. The CSRS AUROC for any serious outcome was 0.72 (95% CI, 0.67-0.78). A low-risk score (CSRS