Clinical Investigation
Correlation between the TIMI risk score and high-risk angiographic findings in non–ST-elevation acute coronary syndromes: Observations from the Platelet Receptor Inhibition in Ischemic Syndrome Management in Patients Limited by Unstable Signs and Symptoms (PRISM-PLUS) trial

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Background

The TIMI risk score for unstable angina and non-ST elevation myocardial infarction is an effective tool for predicting the risk of death and ischemic events among patients with non-ST elevation acute coronary syndromes, as well as for identifying those who are likely to benefit most from low-molecular-weight heparin and glycoprotein IIb/IIIa inhibition.

Methods

To explore the pathobiologic basis for this interaction, we evaluated the relationship between the risk score, assessed at presentation, and angiographic findings among patients with non-ST elevation acute coronary syndromes. Angiographic data regarding thrombus, epicardial flow, and lesion severity were available for 1491 patients from the angiographic substudy of PRISM-PLUS.

Results

Patients with risk scores of 5 to 7 (N = 435) were more likely to have a severe culprit stenosis (81% vs 58%, P < .001) and multivessel disease (80% vs 43%, P < .001) compared to those with scores of 0 to 2 (N = 220). The probability of left main disease (P = .01), visible thrombus, and impaired flow in the culprit lesion also increased progressively with rising risk scores (P < .001). Of the risk indicators that comprise the score, history of coronary disease, advanced age, and ST changes showed the strongest association with severe epicardial disease. Positive biomarkers of necrosis, ST changes, and prior aspirin use emerged as stronger correlates of visible thrombus and/or impaired culprit artery flow.

Conclusions

The TIMI risk score identifies patients who are more likely to have intracoronary thrombus, impaired flow, and increased burden of coronary atherosclerosis. These findings likely explain in part the particular benefit of potent antithrombin and antiplatelet agents among patients with higher risk scores.

Section snippets

Study population

PRISM-PLUS was a multicenter, randomized trial performed in 72 hospitals in 14 countries. The design and results of PRISM-PLUS have been described.8 Briefly, 1915 patients with NSTEACS were enrolled within 12 hours of presentation with severe rest angina (prolonged pain or repetitive episodes), given aspirin, and randomized to 1 of 3 treatment groups: tirofiban plus heparin, tirofiban placebo plus heparin, or tirofiban plus heparin placebo. The protocol required infusion of the study medication

Patients

Core Laboratory interpretation of angiographic data was available for 1491 patients. Angiography was performed a mean of 65 hours after randomization. The baseline risk profile of the population in this substudy was similar to the overall population enrolled in PRISM-PLUS, as assessed using the TIMI risk score4; 15% (n = 220) of patients were in the low-risk (0-2), 56% (n = 836) in the intermediate-risk (3-4), and 29% (n = 435) in the high-risk (5-7) groups. The allocation to each treatment

Discussion

The TIMI risk score is a simple integer score that integrates information from multiple clinical predictors to aid in producing a quantitative estimate of the risk of death and recurrent ischemic events.1 Our present analysis demonstrates associations that may reflect the pathobiologic underpinnings of the TIMI risk score. Specifically, the risk score identified patients who were more likely to have intracoronary thrombus, impaired angiographic flow, and increased burden of coronary

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The PRISM-PLUS trial was supported by Merck & Co, Inc.

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