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Cardiovascular Risk Stratification for Patients Treated With Drug-Eluting Stents: Development and Validation of the
Adriana Costa Moreira1, Amanda Sousa, Jose de Ribamar Costa
1Hospital do Coração (HCOR), Rua Desembargador Eliseu Guilherme, 123, Paraíso, São Paulo, SP - Brazil, CEP 04004-030. moreira.adriana@uol.com.br.
Insights
A new risk score predicts major adverse cardiac events (MACE) after drug-eluting stent (DES) percutaneous coronary intervention (PCI). This score aids in stratifying patients into low, moderate, and high-risk groups for better cardiac event management.
Area of Science:
- Cardiology
- Interventional Cardiology
- Biostatistics
Background:
- Developing accurate risk prediction models is crucial for managing patients undergoing percutaneous coronary intervention (PCI) with drug-eluting stents (DES).
- Major adverse cardiac events (MACE) encompass cardiovascular death, myocardial infarction, and target-lesion revascularization, posing significant risks post-PCI.
- Existing risk stratification tools may not fully capture the complexities of MACE risk in diverse patient populations.
Purpose of the Study:
- To develop and validate a novel risk score for estimating in-hospital and long-term MACE risk following PCI with DES implantation.
- To provide clinicians with a tool for stratifying patients into distinct risk categories (low, moderate, high) for tailored management.
- To improve the prediction of adverse cardiac outcomes across the full spectrum of patient risk profiles.
Main Methods:
- A single-center database of 4061 consecutive patients treated with DES between 2007 and 2014 was utilized.
- The risk score was developed using data from 2863 patients (2007-2012) and validated in 1198 patients (2013-2014).
- Logistic regression and Cox models were employed to develop in-hospital and late follow-up risk scores, respectively, defining MACE as cardiovascular death, myocardial infarction, or ischemia-driven target-lesion revascularization.
Main Results:
- The in-hospital risk score (0-37 points) included factors like age, prior CABG, acute coronary syndrome, peripheral vascular disease, saphenous vein graft treatment, long lesions, small vessels, multivessel disease, and thrombus.
- The late follow-up score (0-45 points) incorporated prior CABG, diabetes mellitus, acute coronary syndrome, multivessel disease, small vessels, ejection fraction <40%, and saphenous vein graft treatment.
- Both scores demonstrated approximately 70% accuracy in predicting MACE and enabled stratification into low-, moderate-, and high-risk groups.
Conclusions:
- A validated risk score has been developed to assess both periprocedural and long-term MACE risk after PCI with DES.
- The score is applicable across a wide range of patient risk profiles and important subgroups.
- This tool supports contemporary risk assessment models for improved patient management post-PCI.
Background:
We sought to develop a risk score to estimate the risk of major adverse cardiac event (MACE) occurrence during the in-hospital and long-term follow-up periods after percutaneous coronary intervention (PCI) with drug-eluting stent (DES) implantation.
Methods:
This score was developed and validated in a single-center database encompassing all consecutive patients treated with DES between 2007 and 2014 (n = 4061). For the development of the score, we analyzed all patients treated between January 2007 and December 2012 (n = 2863) while the validation was conducted in a cohort treated between January 2013 and December 2014 (n = 1198). MACE was defined as the combination of cardiovascular death, myocardial infarction, and ischemia- driven target-lesion revascularization. Different stratification models were developed for the in-hospital (logistic regression) and late follow-up score (Cox model).
Results:
In-hospital scores ranged from 0 to 37 points and comprised: (a) age; (b) previous coronary artery bypass grafting (CABG); (c) acute coronary syndrome; (d) peripheral vascular disease; (e) treatment of saphenous vein graft; (f) long lesions; (g) small vessels; (h) multivessel disease; and (i) thrombus. The late scores ranged from 0 to 45 points and comprised: (a) previous CABG; (b) diabetes mellitus; (c) acute coronary syndrome; (d) multivessel disease; (e) small vessels; (f) ejection fraction <40%; and (g) treatment of saphenous vein graft. Patients were stratified into low-risk, moderate-risk, and high-risk groups. Both scores had close to 70% accuracy for predicting MACE.
Conclusion:
The present score was developed and validated based on contemporary models for assessing periprocedural and long-term MACE risk post PCI, throughout the full spectrum of patient risk, and important patient subgroups.
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