Implications of five different risk models in primary prevention guidelines

Author:

Sud Maneesh12345ORCID,Sivaswamy Atul4,Austin Peter C234,Abdel-Qadir Husam23456,Anderson Todd J78,Naimark David M J2345,Lee Douglas S23459ORCID,Roifman Idan12345,Thanassoulis George1011,Tu Karen23121314,Wijeysundera Harindra C12345,Ko Dennis T12345

Affiliation:

1. Schulich Heart Program, Sunnybrook Health Sciences Centre, University of Toronto , 2075 Bayview Ave, Toronto, Ontario, M4N3M5 , Canada

2. Institute of Health Policy Management , and Evaluation, , 155 College St 4th Floor, Toronto, ON M5T 3M6 , Canada

3. University of Toronto , and Evaluation, , 155 College St 4th Floor, Toronto, ON M5T 3M6 , Canada

4. ICES , Toronto , Canada

5. Department of Medicine, University of Toronto , 2075 Bayview Ave V Wing, Toronto, ON M4N 3M5 , Canada

6. Women's College Hospital, University of Toronto , 76 Grenville St, Toronto, ON M5S 1B2 , Canada

7. Libin Cardiovascular Institute of Alberta , 3310 Hospital Drive NW Calgary, Alberta T2N 4N1 , Canada

8. Cumming School of Medicine, University of Calgary , 3330 Hospital Dr NW, Calgary, AB T2N 4N1 , Canada

9. Peter Munk Cardiac Centre, University Health Network, University of Toronto , 585 University Ave, Toronto, ON M5G 2N2 , Canada

10. Department of Medicine, McGill University , 1001 Decarie Boulevard, suite D05-2212 Montreal (Quebec) H4A 3J1 Canada, Canada

11. Preventive and Genomic Cardiology, McGill University Health Centre , 1001 Decarie Blvd. Montreal, Quebec H4A 3J1 , Canada

12. North York General Hospital , Toronto Western Family Health Team, , 440 Bathurst Street Toronto, ON M5T 2S6 , Canada

13. University Health Network, University of Toronto , Toronto Western Family Health Team, , 440 Bathurst Street Toronto, ON M5T 2S6 , Canada

14. Department of Family and Community Medicine, University of Toronto , 500 University Ave Toronto, ON M5G 1V7 , Canada

Abstract

Abstract Background A lack of consensus exists across guidelines as to which risk model should be used for the primary prevention of cardiovascular disease (CVD). Our objective was to determine potential improvements in the number needed to treat (NNT) and number of events prevented (NEP) using different risk models in patients eligible for risk stratification. Methods and results A retrospective observational cohort was assembled from primary care patients in Ontario, Canada, between 1 January 2010 and 31 December 2014 and followed for up to 5 years. Risk estimation was undertaken in patients 40–75 years of age, without CVD, diabetes, or chronic kidney disease using the Framingham Risk Score (FRS), the Pooled Cohort Equations (PCEs), a recalibrated FRS (R-FRS), the Systematic Coronary Risk Evaluation 2 (SCORE2), and the low-risk region recalibrated SCORE2 (LR-SCORE2). The cohort consisted of 47 399 patients (59% women, mean age 54 years). The NNT with statins was lowest for the SCORE2 at 40, followed by the LR-SCORE2 at 41, the R-FRS at 43, the PCEs at 55, and the FRS at 65. Models that selected for individuals with a lower NNT recommended statins to fewer, but higher-risk patients. For instance, the SCORE2 recommended statins to 7.9% of patients (5-year CVD incidence 5.92%). The FRS, however, recommended statins to 34.6% of patients (5-year CVD incidence 4.01%). Accordingly, the NEP was highest for the FRS at 406 and lowest for the SCORE2 at 156. Conclusions Newer models such as the SCORE2 may improve statin allocation to higher-risk groups with a lower NNT but prevent fewer events at the population level.

Funder

Ontario Ministry of Health and Long-Term Care

Canadian Institutes of Health Research

Cardiovascular Research Fund, Tokyo

Publisher

Oxford University Press (OUP)

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