Centre for Research in Evidence-Based Practice, Bond University, Gold Coast, QLD.
Baker IDI Heart and Diabetes Institute, Melbourne, VIC.
Med J Aust. 2019 Mar;210(4):161-167. doi: 10.5694/mja2.12061. Epub 2019 Jan 18.
To evaluate the performance of the 2013 Pooled Cohort Risk Equation (PCE-ASCVD) for predicting cardiovascular disease (CVD) in an Australian population; to compare this performance with that of three frequently used Framingham-based CVD risk prediction models.
Prospective national population-based cohort study.
42 randomly selected urban and non-urban areas in six Australian states and the Northern Territory.
5453 adults aged 40-74 years enrolled in the Australian Diabetes, Obesity and Lifestyle study and followed until November 2011. We excluded participants who had CVD at baseline or for whom data required for risk model calculations were missing.
Predicted and observed 10-year CVD risks (adjusted for treatment drop-in); performance (calibration and discrimination) of four CVD risk prediction models: 1991 Framingham, 2008 Framingham, 2008 office-based Framingham, 2013 PCE-ASCVD.
The performance of the 2013 PCE-ASCVD model was slightly better than 1991 Framingham, and each was better the two 2008 Framingham risk models, both in men and women. However, all four models overestimated 10-year CVD risk, particularly for patients in higher deciles of predicted risk. The 2013 PCE-ASCVD (7.5% high risk threshold) identified 46% of men and 18% of women as being at high risk; the 1991 Framingham model (20% threshold) identified 17% of men and 2% of women as being at high risk. Only 16% of men and 11% of women identified as being at high risk by the 2013 PCE-ASCVD experienced a CV event within 10 years.
The 2013 PCE-ASCVD or 1991 Framingham should be used as CVD risk models in Australian. However, the CVD high risk threshold for initiating CVD primary preventive therapy requires reconsideration.
评估 2013 年 pooled cohort risk equation(PCE-ASCVD)在澳大利亚人群中预测心血管疾病(CVD)的性能;并与三种常用的基于Framingham 的 CVD 风险预测模型进行比较。
前瞻性全国人群队列研究。
澳大利亚六个州和北领地的 42 个随机选择的城市和非城市地区。
澳大利亚糖尿病、肥胖和生活方式研究中招募的 5453 名年龄在 40-74 岁之间的成年人,随访至 2011 年 11 月。我们排除了基线时患有 CVD 或需要计算风险模型数据的参与者。
预测和观察到的 10 年 CVD 风险(调整治疗中断);四种 CVD 风险预测模型的性能(校准和区分):1991 年Framingham、2008 年Framingham、2008 年基于办公室的Framingham、2013 年 PCE-ASCVD。
2013 年 PCE-ASCVD 模型的性能略优于 1991 年Framingham,在男性和女性中,每个模型都优于两个 2008 年Framingham 风险模型。然而,所有四个模型都高估了 10 年 CVD 风险,特别是在预测风险较高的患者中。2013 年 PCE-ASCVD(7.5%高风险阈值)确定 46%的男性和 18%的女性为高风险;1991 年Framingham 模型(20%的阈值)确定 17%的男性和 2%的女性为高风险。只有 16%的男性和 11%的女性被 2013 年 PCE-ASCVD 识别为高风险,但在 10 年内经历了 CV 事件。
在澳大利亚,应使用 2013 年 PCE-ASCVD 或 1991 年Framingham 作为 CVD 风险模型。然而,需要重新考虑启动 CVD 一级预防治疗的 CVD 高风险阈值。