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May 23, 2017BMJ1,750 citationsOpen Access

Development and validation of QRISK3 risk prediction algorithms to estimate future risk of cardiovascular disease: prospective cohort study

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JHJulia Hippisley–CoxCCCarol CouplandPBPeter Brindle

Key Result

In women, QRISK3 predicted cardiovascular disease risk with a mean 10 year risk of 4.7% and an observed risk of 5.8%, while in men, the predicted risk was 6.4% with an observed risk of 7.5%.

Key Points

  • The aim is to develop and validate the QRISK3 risk prediction algorithms to estimate 10-year cardiovascular disease risk by incorporating new risk factors.
  • Prospective open cohort study involving 1309 general practices in England.
  • Cox proportional hazards models used to develop separate risk equations for men and women.
  • Validation of scores done using a separate cohort of 328 practices.
  • Identified 363,565 incident cases of cardiovascular disease during follow-up from 50.8 million person years of observation.
  • QRISK3 explained 59.6% variation in women and 54.8% in men, indicating good model calibration and discrimination.
  • Overall performance of QRISK3 algorithms was similar to QRISK2, with inclusion of additional clinical variables enhancing prediction.

Study Design

Type

Cohort (n=2,680,478)

Multicenter

Yes

Structured PICO

Does the updated QRISK3 algorithm accurately predict the 10-year risk of cardiovascular disease in adults aged 25-84 years without prior cardiovascular disease?

P
Population
10,561,101 patients (7,889,803 in derivation cohort, 2,671,298 in validation cohort) aged 25-84 years from 1,309 general practices in England. Key inclusion: free of cardiovascular disease and not prescribed statins at baseline.
I
Intervention
QRISK3 risk prediction algorithm (incorporating new risk factors including CKD stage 3-5, systolic blood pressure variability, migraine, corticosteroids, systemic lupus erythematosus, atypical antipsychotics, severe mental illness, and erectile dysfunction)
C
Comparator
QRISK2 algorithm (Model A)
O
Outcome
Incident cardiovascular disease (composite of coronary heart disease, ischaemic stroke, or transient ischaemic attack) recorded on general practice, mortality, or hospital admission recordscomposite

The updated QRISK3 algorithm, incorporating additional clinical variables such as CKD, blood pressure variability, and specific comorbidities, accurately predicts 10-year cardiovascular risk and performs similarly overall to QRISK2 while enabling better identification of risk in specific patient subgroups.

Main Result

Effect estimate: null (95% CI null)

Absolute Event Rate: 4.7% vs 6.4%

p-value: p=null

Limitations

  • Only considered patients in England; results may not be generalizable to other populations.
  • Data primarily from general practices may be subject to recording biases.

Abstract

Objectives To develop and validate updated QRISK3 prediction algorithms to estimate the 10 year risk of cardiovascular disease in women and men accounting for potential new risk factors.Design Prospective open cohort study.Setting General practices in England providing data for the QResearch database.Participants 1309 QResearch general practices in England: 981 practices were used to develop the scores and a separate set of 328 practices were used to validate the scores. 7.89 million patients aged 25-84 years were in the derivation cohort and 2.67 million patients in the validation cohort. Patients were free of cardiovascular disease and not prescribed statins at baseline.Methods Cox proportional hazards models in the derivation cohort to derive separate risk equations in men and women for evaluation at 10 years. Risk factors considered included those already in QRISK2 (age, ethnicity, deprivation, systolic blood pressure, body mass index, total cholesterol: high density lipoprotein cholesterol ratio, smoking, family history of coronary heart disease in a first degree relative aged less than 60 years, type 1 diabetes, type 2 diabetes, treated hypertension, rheumatoid arthritis, atrial fibrillation, chronic kidney disease (stage 4 or 5)) and new risk factors (chronic kidney disease (stage 3, 4, or 5), a measure of systolic blood pressure variability (standard deviation of repeated measures), migraine, corticosteroids, systemic lupus erythematosus (SLE), atypical antipsychotics, severe mental illness, and HIV/AIDs). We also considered erectile dysfunction diagnosis or treatment in men. Measures of calibration and discrimination were determined in the validation cohort for men and women separately and for individual subgroups by age group, ethnicity, and baseline disease status.Main outcome measures Incident cardiovascular disease recorded on any of the following three linked data sources: general practice, mortality, or hospital admission records.Results 363 565 incident cases of cardiovascular disease were identified in the derivation cohort during follow-up arising from 50.8 million person years of observation. All new risk factors considered met the model inclusion criteria except for HIV/AIDS, which was not statistically significant. The models had good calibration and high levels of explained variation and discrimination. In women, the algorithm explained 59.6% of the variation in time to diagnosis of cardiovascular disease (R2, with higher values indicating more variation), and the D statistic was 2.48 and Harrell's C statistic was 0.88 (both measures of discrimination, with higher values indicating better discrimination). The corresponding values for men were 54.8%, 2.26, and 0.86. Overall performance of the updated QRISK3 algorithms was similar to the QRISK2 algorithms.Conclusion Updated QRISK3 risk prediction models were developed and validated. The inclusion of additional clinical variables in QRISK3 (chronic kidney disease, a measure of systolic blood pressure variability (standard deviation of repeated measures), migraine, corticosteroids, SLE, atypical antipsychotics, severe mental illness, and erectile dysfunction) can help enable doctors to identify those at most risk of heart disease and stroke.

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Cite This Study

Hippisley–Cox et al. (2017) conducted a cohort in cardiovascular disease (n=2,680,478). QRISK3 risk prediction algorithms vs. QRISK2 algorithms was evaluated on 10 year risk of cardiovascular disease (null, 95% CI null, p=null). In women, QRISK3 predicted cardiovascular disease risk with a mean 10 year risk of 4.7% and an observed risk of 5.8%, while in men, the predicted risk was 6.4% with an observed risk of 7.5%.

synapsesocial.com/papers/6970e34ae46c5fd093946dc0https://doi.org/10.1136/bmj.j2099
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