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Published on: August 9, 2024
Precise Score Validation in Buenos Aires 1 Registry
Florencia Muñoz1, Marcos Viruel1, Cristian Garmendia1
1Ischemic Heart Desease Program of Instituto Cardiovascular (ICBA), Buenos Aires, Argentina.
The PRECISE-DAPT score effectively identifies patients at high risk of bleeding and thrombotic events after non-ST elevation acute coronary syndromes. A score of 25 or higher signals increased risk for these adverse outcomes.
Area of Science:
- Cardiology
- Clinical Risk Prediction
Background:
- Dual antiplatelet therapy (DAPT) is crucial after percutaneous coronary intervention (PCI).
- Predicting bleeding risk in patients with non-ST elevation acute coronary syndromes (NSTE-ACS) on DAPT is essential for optimal management.
Purpose of the Study:
- To evaluate the predictive performance of the PRECISE-DAPT score for bleeding events and major adverse cardiovascular events (MACE) in NSTE-ACS patients undergoing DAPT.
- To assess the utility of the PRECISE-DAPT score in identifying high-risk patient subgroups.
Main Methods:
- Analysis of 862 NSTE-ACS patients from the Buenos Aires 1 registry.
- Calculation of the PRECISE-DAPT score upon admission.
- 15-month follow-up to assess bleeding events (BARC 2, 3, or 5) and MACE.
- Evaluation of the score as both a continuous and dichotomous variable (≥25).
Main Results:
- As a continuous variable, the PRECISE-DAPT score showed low to moderate predictive ability for BARC 2, 3, or 5 bleeding (c-statistic 0.58) and moderate ability for BARC 3 or 5 bleeding (c-statistic 0.72).
- The score demonstrated poor prediction for MACE (c-statistic 0.49).
- A dichotomous PRECISE-DAPT score ≥25 (24% of patients) was associated with significantly higher risks of both bleeding (HR 2.1) and ischemic events (HR 1.9).
Conclusions:
- The PRECISE-DAPT score, particularly when dichotomized at ≥25, effectively identifies a subgroup of NSTE-ACS patients at high risk for both bleeding and thrombotic events.
- This score can aid clinicians in tailoring DAPT duration and intensity in high-risk NSTE-ACS populations.
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