...
首页> 外文期刊>IJC Heart & Vasculature >Comparative performance of pooled cohort equations and Framingham risk scores in cardiovascular disease risk classification in a slum setting in Nairobi Kenya
【24h】

Comparative performance of pooled cohort equations and Framingham risk scores in cardiovascular disease risk classification in a slum setting in Nairobi Kenya

机译:在内罗毕肯尼亚的贫民窟环境中汇集队列群体风险分数的汇集队列方程和框架风险评分的比较表现

获取原文
           

摘要

BackgroundCardiovascular diseases (CVD) cause 18 million deaths annually. Low- and middle-income countries (LMICs) account for 80% of the CVD burden, and the burden is expected to grow in the region in the coming years. Screening for and identification of individuals at high risk for CVD in primary care settings can be accomplished using available CVD risk scores. However, few of these scores have been validated/recalibrated for use in sub-Saharan Africa (SSA).MethodsPooled cohort equations (PCE) and Framingham risk scores for 10-year CVD risk were applied on 1960 men and women aged 40?years and older from the AWI-Gen (Africa, Wits-INDEPTH Partnership for GENomic studies) study 2015. Low, moderate/intermediate or high CVD risk classifications correspond to <10%, 10–20% and >20% chance of developing CVD in 10?years respectively. Agreement between the risk scores was assessed using kappa and correlation coefficients.ResultsHigh CVD risk was 10.3% in PCE 2013, 0.4% in PCE 2018, 2.9% in Framingham and 3.6% in Framingham non-laboratory scores. Conversely, low CVD risk was 62.2% in PCE 2013 and 95.6% in PCE 2018, 84.0% and 80.1% in Framingham and Framingham non-laboratory scores, respectively. A moderate agreement existed between the Framingham functions (kappa?=?0.64, 95% CI 0.59–0.68, correlation, rs?=?0.711). There was no agreement between the PCE 2013 and 2018 functions (kappa?=?0.05, 95% CI 0.04–0.06).ConclusionsNewer cohort-based data is necessary to validate and recalibrate existing CVD risk scores in order to develop appropriate functions for use in SSA.
机译:背景卡血管疾病(CVD)每年引起1800万人死亡。低收入和中等收入国家(LMICS)占CVD负担的80%,预计未来几年将在该地区增长。可以使用可用的CVD风险评分来完成在初级保健环境中为CVD的高风险筛选和鉴定个体。然而,在撒哈拉以南非洲(SSA)中,这些分数很少有验证/重新校准.Methodpooled队列的队列(PCE)和90年代男性和女性的10年的CVD风险的Framingham风险分数适用于40岁的男性和女性从AWI-Gen(非洲,基因组研究的智权伙伴关系)研究2015年。低,中/中等或高CVD风险分类对应于10%的10%,10-20%和> 20%的机会在10中开发CVD ?分别为多年。使用Kappa和相关系数评估风险评分之间的一致性。PCE 2013年的CVD风险为10.3%,PCE 2018年的0.4%,弗拉姆汉姆非实验室评分为3.6%。相反,PCE 2013年的低CVD风险为62.2%,PCE 2018年的95.6%,分别为95.6%,分别在弗拉姆和弗兰明翰非实验室评分中的84.0%和80.1%。在框架函数之间存在适度的协议(κλ=?= 0.64,95%CI 0.59-0.68,相关性,Rs?= 0.711)。 PCE 2013和2018函数之间没有达成协议(kappa?=?0.05,95%CI 0.04-0.06)。ConclusionsNewer队列基于群组的数据是必要的,以验证和重新校准现有的CVD风险分数,以便制定适当的使用功能SSA。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号