Clinical Implications of Revised Pooled Cohort Equations for Estimating Atherosclerotic Cardiovascular Disease Risk

被引:156
作者
Yadlowsky, Steve [1 ]
Hayward, Rodney A. [2 ,3 ,10 ]
Sussman, Jeremy B. [2 ,3 ,11 ]
McClelland, Robyn L. [4 ]
Min, Yuan-, I [5 ,6 ]
Basu, Sanjay [1 ,7 ,8 ,9 ]
机构
[1] Stanford Univ, Ctr Primary Care & Outcomes Res, 616 Serra St,Room E012, Stanford, CA 94305 USA
[2] Univ Michigan, Ann Arbor, MI 48109 USA
[3] Vet Affairs Ann Arbor Healthcare Syst, Ctr Clin Management Res, Ann Arbor, MI USA
[4] Univ Washington, 6200 NE 74th St, Seattle, WA 98195 USA
[5] Univ Mississippi, Med Ctr, 350 West Woodrow Wilson Ave,Suite 701, Jackson, MS 39213 USA
[6] Jackson Heart Study, Jackson, MS USA
[7] Stanford Univ, Ctr Populat Hlth Sci, Stanford, CA 94305 USA
[8] Harvard Med Sch, Ctr Primary Care, Boston, MA USA
[9] Stanford Univ, 117 Crothers Way, Stanford, CA 94305 USA
[10] VA Ann Arbor Hlth Care, 2800 Plymouth Rd,Bldg 14,G100-36, Ann Arbor, MI 48109 USA
[11] VA Ann Arbor Hlth Care, 2800 Plymouth Rd,Bldg 16,Room 335E, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
AMERICAN-COLLEGE; TASK-FORCE; CALIBRATION; PREVENTION; VALIDATION; STATINS; MODELS;
D O I
10.7326/M17-3011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The 2013 pooled cohort equations (PCEs) are central in prevention guidelines for cardiovascular disease (CVD) but can misestimate CVD risk. Objective: To improve the clinical accuracy of CVD risk prediction by revising the 2013 PCEs using newer data and statistical methods. Design: Derivation and validation of risk equations. Setting: Population-based. Participants: 26 689 adults aged 40 to 79 years without prior CVD from 6 U.S. cohorts. Measurements: Nonfatal myocardial infarction, death from coronary heart disease, or fatal or nonfatal stroke. Results: The 2013 PCEs overestimated 10-year risk for atherosclerotic CVD by an average of 20% across risk groups. Misestimation of risk was particularly prominent among black adults, of whom 3.9 million (33% of eligible black persons) had extreme risk estimates (<70% or >250% those of white adults with otherwise-identical risk factor values). Updating these equations improved accuracy among all race and sex subgroups. Approximately 11.8 million U. S. adults previously labeled high-risk (10year risk >= 7.5%) by the 2013 PCEs would be relabeled lower-risk by the updated equations. Limitations: Updating the 2013 PCEs with data from modern cohorts reduced the number of persons considered to be at high risk. Clinicians and patients should consider the potential benefits and harms of reducing the number of persons recommended aspirin, blood pressure, or statin therapy. Our findings also indicate that risk equations will generally become outdated over time and require routine updating. Conclusion: Revised PCEs can improve the accuracy of CVD risk estimates.
引用
收藏
页码:20 / +
页数:11
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