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Laboratory and non-laboratory-based risk prediction models for secondary prevention of cardiovascular disease: the
Jisheng Cui1, Andrew Forbes, Adrienne Kirby
1Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia. jisheng.cui@deakin.edu.au
Insights
Simple non-laboratory risk models effectively predict recurrent cardiovascular disease (CVD) events. These models, using factors like age and BMI, offer a valuable clinical tool for assessing patient risk.
Area of Science:
- Cardiology
- Preventive Medicine
- Biostatistics
Background:
- Recurrent cardiovascular disease (CVD) events pose a significant health burden.
- Accurate risk prediction is crucial for effective patient management and secondary prevention.
Purpose of the Study:
- To evaluate the prognostic value of risk prediction models for recurrent CVD events.
- To assess the performance of models utilizing non-laboratory data.
- To develop a risk chart for clinical use.
Main Methods:
- Cox proportional hazards models were employed to calculate risk scores in a large clinical trial cohort.
- Models were validated using calibration and discrimination analyses on data from New Zealand.
- Risk factors including age, sex, BMI, smoking, and medical history were analyzed.
Main Results:
- Non-laboratory risk factors demonstrated significant association with recurrent CVD events.
- Patients in medium and high-risk groups showed a 2-fold and 4-fold increased risk, respectively, compared to the low-risk group.
- Validated models accurately predicted risk in independent datasets.
Conclusions:
- Simpler, non-laboratory-based risk prediction models are as effective as comprehensive laboratory-based models.
- A simplified risk chart can serve as a practical tool for clinicians to assess individual CVD event risk.
Aims:
The aims of this study were to examine whether risk prediction models for recurrent cardiovascular disease (CVD) events have prognostic value, and to particularly examine the performance of those models based on non-laboratory data. We also aimed to construct a risk chart based on the risk factors that showed the strongest relationship with CVD.
Methods And Results:
Cox proportional hazards models were used to calculate a risk score for each recurrent event in a CVD patient who was enrolled in a very large randomized controlled clinical trial. Patients were then classified into groups according to quintiles of their risk score. These risk models were validated by calibration and discrimination analyses based on data from patients recruited in New Zealand for the same study. Non-laboratory-based risk factors, such as age, sex, body mass index, smoking status, angina grade, history of myocardial infarction, revascularization, stroke, diabetes or hypertension and treatment with pravastatin, were found to be significantly associated with the risk of developing a recurrent CVD event. Patients who were classified into the medium and high-risk groups had two-fold and four-fold the risk of developing a CVD event compared with those in the low-risk group, respectively. The risk prediction models also fitted New Zealand data well after recalibration.
Conclusion:
A simpler non-laboratory-based risk prediction model performed equally as well as the more comprehensive laboratory-based risk prediction models. The risk chart based on the further simplified Score Model may provide a useful tool for clinical cardiologists to assess an individual patient's risk for recurrent CVD events.
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