AHA PREVENT-ASCVD Risk Calculator
Estimate 10-year and age-eligible 30-year risk of a first ASCVD event with the corrected AHA PREVENT base equations.
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For a clinician-reviewed primary-prevention discussion
ASCVD means atherosclerotic cardiovascular disease: disease caused by plaque in arteries that can lead to myocardial infarction or stroke. Enter current measurements and explicitly complete every selector. The result estimates risk in a population model; it does not inspect arteries, diagnose disease, or tell an individual which test or treatment to use.
About
The corrected AHA PREVENT-ASCVD base equations estimate the probability of a first atherosclerotic cardiovascular disease event—fatal or nonfatal myocardial infarction or stroke—over 10 years and, when age-eligible, 30 years. They are sex-specific, race-free population models developed from contemporary U.S. cohorts, not a diagnosis or a certainty for one person. [1, 2]
This page implements only the corrected ASCVD base equations for adults ages 30–79 without established cardiovascular disease or heart failure. It does not calculate PREVENT-CVD, PREVENT-HF, optional UACR, HbA1c, or social-deprivation models, PREVENT-Age, a 30-year PREVENT-CVD percentile, or treatment effect. [3, 4, 5]
The 10-year model is available from ages 30–79; the 30-year model is limited to ages 30–59. A percentage describes outcomes observed in people with similar modeled characteristics. It cannot inspect arteries, detect subclinical plaque or a prior silent event, or determine an individual future. [1, 5]
Formula
Interpretation
What the percentage represents
The result estimates how often a first ASCVD event occurred over the stated time horizon among people with similar modeled characteristics. A 3.6% estimate is not a predetermined 3.6% fate for one person. Both underestimation and overestimation are possible, and the model cannot diagnose myocardial infarction, stroke, coronary disease, plaque, or heart failure. Use current, clinician-verified values from the same assessment period. [1, 3]
Published worked example
In the original PREVENT report, a 50-year-old woman with total cholesterol 240 mg/dL, HDL-C 55 mg/dL, treated systolic blood pressure 160 mmHg, no statin use, no diabetes, no current smoking, and eGFR 90 mL/min/1.73 m² had an ASCVD base estimate of about 3.6% at 10 years and 20% at 30 years. This page reproduces 3.6% and 19.9% before the paper’s whole-number rounding. It is an equation check, not a normal reference patient. [1, 2]
2026 dyslipidemia categories are conditional context
| 10-year PREVENT-ASCVD estimate | Static guideline term |
|---|---|
| <3% | Low |
| 3% to <5% | Borderline |
| 5% to <10% | Intermediate |
| ≥10% | High |
The 2026 U.S. dyslipidemia guideline applies these terms in a specific lipid-management context: adults without known ASCVD or subclinical atherosclerosis and with LDL-C 70–189 mg/dL. This page does not collect LDL-C or establish whether subclinical atherosclerosis is absent, so it does not dynamically label a submitted result or turn the percentage into a medication, nonstatin therapy, or coronary calcium recommendation. The static context can support clinician–patient shared decision-making only after the applicable pathway is established. [7, 8, 9]
Base ASCVD versus other cardiovascular tools
PREVENT-ASCVD predicts a first ASCVD event. The full AHA PREVENT tool can also calculate total CVD and heart-failure outcomes and can use optional UACR, HbA1c, or social-deprivation inputs. The historical Framingham General CVD calculator uses different predictors, endpoints, populations, and calibration. Its percentage is not interchangeable with this result. The full AHA tool also provides PREVENT-Age and a 30-year PREVENT-CVD percentile; neither can be derived from this page’s ASCVD percentage. [4, 5]
Limits and appropriate use
PREVENT was developed from U.S. data. A 2026 multinational validation included 6,422,714 people across 44 observational cohorts and 18 randomized trials and found generally useful performance, but calibration varied by region. ASCVD evidence from Asia and other underrepresented regions was more limited, so the study does not prove identical accuracy in every country, health system, population, or person. This page cannot perform local recalibration. [10]
Inputs used by this ASCVD base model
| Input | Meaning on this page | Technical range or state |
|---|---|---|
| Sex coefficient | The published female or male coefficient set; it does not infer gender identity, chromosomes, hormone status, or another coefficient. | Female or male set |
| Age | Completed years at the current assessment. | 30–79 years |
| Total cholesterol and HDL-C | Current reliable values from the same assessment period; non-HDL-C is calculated as total cholesterol minus HDL-C. | TC 130–320; HDL-C 20–100 mg/dL |
| Systolic blood pressure | A representative current systolic measurement. | 90–200 mmHg |
| eGFR | A current clinically reported estimate; this page does not calculate eGFR from creatinine. | 15–140 mL/min/1.73 m² |
| Current BP treatment | Whether antihypertensive medicine is currently used. | Yes or No |
| Current statin use | Whether a statin is currently used; this is not a treatment recommendation. | Yes or No |
| Diabetes | The documented diabetes-history input used by the model. | Yes or No |
| Current smoking | Cigarette use within the previous 30 days; it does not quantify pack-years or all nicotine exposure. | Yes or No |
These limits are the implemented model’s technical input ranges, not healthy ranges, treatment targets, diagnoses, or a reason to substitute the nearest boundary. This calculator rejects an out-of-range value instead of silently capping it. [5, 6]
Model identity, correction, and reproducibility
The original methods report describes the endpoint, cohorts, predictors, splines, interactions, and sex-specific logistic models. A separate formal correction supplies corrected equation material; this implementation identifies that corrected model explicitly and retains full precision until display. The two publications are listed separately so the correction is not hidden inside the original citation. [1, 2]
What the complete AHA tool does that this page does not
The AHA PREVENT family has separate outcome equations for total cardiovascular disease, ASCVD, and heart failure, plus optional predictors in expanded models. The current official tool can also present PREVENT-Age and a 30-year PREVENT-CVD percentile. Those outputs require their own definitions and models. This page does not treat missing UACR, HbA1c, or ZIP-code/SDI data as zero and does not derive any of those outputs from the ASCVD base percentage. [3, 4, 5]
Different guidelines use different PREVENT outcomes
The 2026 U.S. dyslipidemia pathway uses PREVENT-ASCVD in its defined primary-prevention context. By contrast, the 2025 U.S. blood-pressure guideline’s 7.5% decision threshold refers to 10-year total CVD from PREVENT-CVD, not this page’s ASCVD-specific output. The two endpoints are not interchangeable, and this page does not apply that 7.5% threshold. [6, 7, 8]
Why the selectors are not a treatment simulator
Blood-pressure treatment, statin use, smoking, diabetes, and measurements must describe the actual current assessment. Changing a selector to create a hypothetical second result does not estimate the causal effect of starting or stopping therapy, stopping smoking, or changing a laboratory value. The difference between two runs is not treatment benefit and cannot select a medicine, dose, coronary calcium scan, or care plan. [3, 9]
Calibration and individual limitations
Even a well-performing population model can overestimate or underestimate absolute risk for a particular person or setting. The multinational validation supports transportability across many cohorts while also documenting regional variation and thinner evidence in some regions. Interpretation still depends on local calibration, current measurements, known or subclinical disease, LDL-C and other risk enhancers, competing illness, and patient preferences. [9, 10]
References
- Khan SS, Matsushita K, Sang Y, et al. Development and Validation of the American Heart Association’s PREVENT Equations. Circulation. 2024;149(6):430–449. PMID 37947085. PMCID PMC10910659. DOI 10.1161/CIRCULATIONAHA.123.067626.
- Correction to: Development and Validation of the American Heart Association’s PREVENT Equations. Circulation. 2024;149(11):e956. PMID 38466792. DOI 10.1161/CIR.0000000000001230.
- Khan SS, Coresh J, Pencina MJ, et al. Novel Prediction Equations for Absolute Risk Assessment of Total Cardiovascular Disease Incorporating Cardiovascular-Kidney-Metabolic Health: A Scientific Statement From the American Heart Association. Circulation. 2023;148(24):1982–2004. PMID 37947094. DOI 10.1161/CIR.0000000000001191.
- American Heart Association. Predicting Risk of cardiovascular disease EVENTs (PREVENT) Calculator. Official model and implementation information.
- American Heart Association. PREVENT Equations Quickstart Guide. 2026.
- American Heart Association. PREVENT Equations Frequently Asked Questions. Current guideline-use FAQ.
- Blumenthal RS, Morris PB, Gaudino M, et al. 2026 ACC/AHA/AACVPR/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Dyslipidemia. Circulation. 2026;153:e1154–e1276. DOI 10.1161/CIR.0000000000001423.
- Correction to: 2026 ACC/AHA/AACVPR/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Dyslipidemia. Circulation. 2026. PMID 42330109. DOI 10.1161/CIR.0000000000001457.
- American Heart Association. Top Take-Home Messages for Clinicians: Using PREVENT-ASCVD Equations for Risk-Based Lipid Management. 2026.
- Neuen BL, Major RW, Grams ME, et al. Multinational validation of the PREVENT and SCORE2 cardiovascular risk equations across 6.4 million individuals. Nature Medicine. 2026. PMID 42086979. DOI 10.1038/s41591-026-04437-z.
FAQ
It estimates the probability of a first atherosclerotic cardiovascular disease event over 10 years and, when age-eligible, 30 years. The modeled endpoint includes fatal or nonfatal myocardial infarction or stroke. It is a population-model estimate, not a diagnosis or a certainty for one person.
PREVENT-ASCVD models first atherosclerotic events. PREVENT-CVD combines ASCVD and heart-failure outcomes, while PREVENT-HF models heart failure. They have different predictor terms and endpoints, so their percentages are not interchangeable. This page implements only the ASCVD base equations.
They record the actual current treatment status at the time of the assessment because treatment status is part of the published equation. They are not controls for simulating starting or stopping treatment. The difference between two calculations is not an estimate of treatment benefit or the expected change in risk, and neither result is a prescription.
The 2026 U.S. dyslipidemia guideline uses low below 3%, borderline from 3% to below 5%, intermediate from 5% to below 10%, and high at 10% or above in a specific context: adults without known ASCVD or subclinical atherosclerosis and with LDL-C 70–189 mg/dL. Because this page does not establish those conditions, it shows the terms only as static context and does not dynamically classify a result.
No. A risk estimate is one input to a clinician–patient discussion. LDL-C, known or subclinical disease, diabetes, kidney disease, familial hypercholesterolemia, other risk enhancers, possible coronary calcium testing, competing conditions, medication tolerance, and patient preferences can change the applicable pathway. This page does not select a medicine, dose, test, or treatment.
The equations were developed and validated in U.S. adults. Multinational studies support useful discrimination in several settings, but calibration can vary by country and population. An estimate outside the U.S. therefore needs local clinical context and should not be assumed to have identical calibration.
This page implements the base ASCVD equations only. PREVENT also has optional expanded equations that can incorporate urine albumin-to-creatinine ratio, hemoglobin A1c, or a social deprivation index when available. Those are different model variants and are not silently substituted here.
No. PREVENT-ASCVD uses a contemporary race-free model, includes eGFR, and has different endpoints, populations, coefficients, and calibration. Framingham General CVD and the older Pooled Cohort Equations produce different risk estimates that should not be compared as if they were the same scale.
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Disclaimer
Educational and informational reference only. Not intended to replace professional medical advice, diagnosis, treatment, or independent verification.