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Prediction of Cardiovascular and All-Cause Mortality After Myocardial Infarction in US Veterans
Bing Lu1, Daniel Posner2, Jason L Vassy3
1Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC), Veterans Affairs, Boston Healthcare System, Boston, Massachusetts; Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Public Health Sciences, University of Connecticut School of Medicine, Farmington, Connecticut.
Insights
New risk models predict cardiovascular disease (CVD) death and all-cause mortality in myocardial infarction (MI) survivors. These models identify key risk factors and can guide secondary prevention strategies for improved patient outcomes.
Area of Science:
- Cardiology
- Public Health
- Health Informatics
Background:
- Existing cardiovascular disease (CVD) death risk models may not accurately predict outcomes for myocardial infarction (MI) survivors.
- Accurate mortality risk prediction post-MI is crucial for effective secondary prevention strategies.
Purpose of the Study:
- To develop and internally validate risk prediction models for 5-year CVD death and all-cause mortality in outpatient MI survivors.
- To identify predictors associated with increased or decreased mortality risk in this patient population.
Main Methods:
- Utilized national electronic health record data from the Veterans Health Administration (2002-2012).
- Developed Cox proportional hazards models using follow-up data of 100,601 MI survivors.
- Evaluated model performance using a cross-validation approach.
Main Results:
- Identified key risk factors for CVD and all-cause death in men, including older age, smoking, heart failure, and peripheral artery disease.
- Statin and hypertension medication use, higher estimated glomerular filtration rate, and higher body mass index were associated with reduced mortality risk.
- Similar, yet distinct, predictors were observed in women; models demonstrated good calibration and predictive accuracy (C-statistics ranging from 0.75 to 0.81).
Conclusions:
- Developed and validated 5-year risk prediction models for CVD and all-cause death in MI survivors.
- Traditional risk factors, comorbidities, and undertreatment of hypertension and hyperlipidemia significantly increase mortality risk.
- These models can aid in tailoring secondary prevention for MI survivors.
Abstract:
Risk prediction models for cardiovascular disease (CVD) death developed from patients without vascular disease may not be suitable for myocardial infarction (MI) survivors. Prediction of mortality risk after MI may help to guide secondary prevention. Using national electronic record data from the Veterans Health Administration 2002 to 2012, we developed risk prediction models for CVD death and all-cause death based on 5-year follow-up data of 100,601 survivors of MI using Cox proportional hazards models. Model performance was evaluated using a cross-validation approach. During follow-up, there were 31,622 deaths and 12,901 CVD deaths. In men, older age, current smoking, atrial fibrillation, heart failure, peripheral artery disease, and lower body mass index were associated with greater risk of death from CVD or all-causes, and statin treatment, hypertension medication, estimated glomerular filtration rate level, and high body mass index were significantly associated with reduced risk of fatal outcomes. Similar associations and slightly different predictors were observed in women. The estimated Harrell's C-statistics of the final model versus the cross-validation estimates were 0.77 versus 0.77 in men and 0.81 versus 0.77 in women for CVD death. Similarly, the C-statistics were 0.75 versus 0.75 in men, 0.78 versus 0.75 in women for all-cause mortality. The predicted risk of death was well calibrated compared with the observed risk. In conclusion, we developed and internally validated risk prediction models of 5-year risk for CVD and all-cause death for outpatient survivors of MI. Traditional risk factors, co-morbidities, and lack of blood pressure or lipid treatment were all associated with greater risk of CVD and all-cause mortality.
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