Printed on 2/13/2026
For informational purposes only. This is not medical advice.
The TIMI risk score for NSTEMI/UA uses 7 variables to stratify patients with non-ST elevation ACS. Scores range 0–7 and predict the 14-day risk of death, MI, or need for urgent revascularization, guiding decisions about invasive versus conservative management strategy.
Formula: Each criterion = 1 point. Age ≥65, CAD ≥50%, ASA use 7d, ≥2 angina 24h, ST dev ≥0.5mm, elevated biomarkers, ≥3 RF. Total 0–7.
Your TIMI NSTEMI/UA score predicts the 14-day risk of a composite endpoint: all-cause death, new or recurrent myocardial infarction, or severe recurrent ischemia requiring urgent revascularization. A score of 0-2 indicates low risk (approximately 5-8% event rate), where conservative management with medical therapy and non-invasive stress testing may be appropriate. A score of 3-4 represents moderate risk (13-20%), and a score of 5-7 indicates high risk (26-41%), both of which favor an early invasive strategy with coronary angiography within 24-72 hours.
Each point in the TIMI NSTEMI score carries equal weight, making it simple to calculate at the bedside. However, the presence of elevated cardiac biomarkers (troponin) and ST deviation are particularly strong markers of ongoing ischemia and myocardial necrosis, and their presence should heighten clinical concern regardless of the total score.
Use this score when evaluating patients presenting to the emergency department or chest pain unit with suspected non-ST elevation acute coronary syndrome (NSTEMI or unstable angina). It should be calculated after the initial ECG and troponin results are available. The score helps guide the critical decision of whether to pursue an early invasive strategy (catheterization within 24-72 hours) versus an initially conservative approach (medical management with possible later non-invasive testing).
The TIMI NSTEMI score is also useful for communicating risk to patients and families, for emergency department disposition decisions (admission to monitored bed vs. observation unit), and for identifying patients who may benefit from more aggressive antithrombotic therapy (glycoprotein IIb/IIIa inhibitors, early dual antiplatelet therapy).
The TIMI NSTEMI score was derived from clinical trial populations (TIMI 11B and ESSENCE trials), which may not fully represent real-world emergency department patients. Trial exclusion criteria may have eliminated very high-risk and very low-risk patients, potentially affecting the score's calibration at the extremes.
The score uses binary variables, which limits its discriminative power compared to the GRACE score, which incorporates continuous variables such as age, heart rate, and creatinine. The TIMI score does not account for renal function, hemodynamic status, or heart failure, all of which are important prognostic factors in ACS. For these reasons, the ESC guidelines recommend the GRACE score as the preferred risk stratification tool, though the TIMI score remains widely used due to its simplicity and ease of bedside calculation.
Disclaimer: This tool is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider with questions about your health.
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