Development and Validation of Models to Predict Major Adverse Cardiovascular Events in Chronic Kidney Disease

IF 2.5 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Navdeep Tangri MD, PhD , Thomas W. Ferguson MSc , Ryan J. Bamforth MSc , Manish M. Sood MD, MSc , Pietro Ravani MD, PhD , Alix Clarke Stat MSc , Alessandro Bosi MSc , Juan J. Carrero Pharm PhD
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Abstract

Background

Accurate cardiovascular (CV) risk prediction tools may heighten awareness and monitoring, improve the use of evidence-based therapies and help inform shared decision making for patients with chronic kidney disease (CKD). The purpose of this study was to develop and externally validate a risk prediction model for incident and recurrent CV events across all stages of CKD using commonly available demographics and laboratory data.

Methods

A series of models were developed using administrative and laboratory data (n=36,317) from Manitoba, Canada, between April 1, 2006, and December 31, 2018, with external validation in health system’s data from Alberta, Canada (n=95,191), and Stockholm, Sweden (n=83,000). Adults with incident CKD stages G1-G4 were followed for the occurrence of major adverse cardiovascular events (MACE) (myocardial infraction, stroke, and CV death), and MACE including hospitalization for heart failure (MACE+). Discrimination and calibration were evaluated using the area under the receiver operating characteristic curve (AUC), Brier scores, and plots of observed vs predicted risk, and the models were compared to an existing model from the Chronic Renal Insufficiency Cohort (CRIC).

Results

In the Alberta cohort, the AUCs for predicting MACE and MACE+ were 0.77 (0.77-0.77) and 0.80 (0.79-0.80), respectively. In the Stockholm cohort, the model achieved an AUC of 0.87 (0.86-0.87) for predicting MACE and 0.88 (0.88-0.88) for MACE+. Overall performance was improved relative to CRIC.

Conclusions

A model including commonly available administrative data and laboratory results can predict the risk of MACE and MACE+ outcomes among individuals with CKD.
慢性肾脏疾病主要不良心血管事件预测模型的建立和验证
准确的心血管(CV)风险预测工具可以提高对慢性肾脏疾病(CKD)患者的认识和监测,改善循证治疗的使用,并有助于为共同决策提供信息。本研究的目的是利用常用的人口统计学和实验室数据,开发并外部验证CKD各阶段发生和复发性心血管事件的风险预测模型。方法利用2006年4月1日至2018年12月31日期间来自加拿大马尼托巴省的行政和实验室数据(n=36,317)建立了一系列模型,并对来自加拿大阿尔伯塔省(n= 95191)和瑞典斯德哥尔摩(n=83,000)的卫生系统数据进行了外部验证。随访G1-G4期CKD成人主要不良心血管事件(MACE)(心肌梗死、卒中和CV死亡)的发生情况,MACE包括心力衰竭住院(MACE+)。使用受试者工作特征曲线下面积(AUC)、Brier评分和观察风险与预测风险对照图评估鉴别和校准,并将模型与慢性肾功能不全队列(CRIC)的现有模型进行比较。结果在Alberta队列中,预测MACE和MACE+的auc分别为0.77(0.77-0.77)和0.80(0.79-0.80)。在斯德哥尔摩队列中,该模型预测MACE的AUC为0.87(0.86-0.87),预测MACE+的AUC为0.88(0.88-0.88)。总体表现相对于CRIC有所改善。结论一个包括常用管理数据和实验室结果的模型可以预测CKD患者MACE和MACE+结局的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CJC Open
CJC Open Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.30
自引率
0.00%
发文量
143
审稿时长
60 days
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