一种新的风险评分模型,用于预测肾移植候选者中是否存在严重的冠状动脉疾病。

Luís Henrique Wolff Gowdak, Flávio Jota de Paula, Luiz Antônio Machado César, Luiz Aparecido Bortolotto, José Jayme Galvão de Lima
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引用次数: 10

摘要

背景:肾移植候选人患冠状动脉疾病(CAD)的风险很高。我们试图开发一种新的风险评分模型,以确定肾移植候选者发生显著CAD的测试前概率。方法:对1060名肾移植候选人进行了全面的心血管风险评估。被认为有CAD高风险的患者(年龄≥50岁,患有糖尿病(DM)或心血管疾病(CVD)),或有无创检测提示CAD的患者被转诊进行冠状动脉造影(n=524)。显著的CAD定义为管腔狭窄≥70%。建立了一个二元逻辑回归模型,并将每个变量的逻辑回归系数B乘以10,四舍五入到下一个整数。对于每个患者,计算相应的风险评分,并构建受试者操作特征(ROC)曲线。结果:模型的最终方程为风险评分=(年龄×0.4)+(DM×9)+(CVD×14),CAD的概率(%)=(风险评分×2)-23。CAD诊断准确性的相应ROC为0.75(P结论:我们开发了一个简单的临床风险评分来确定肾移植候选者中发生显著CAD的测试前概率。该模型可能有助于那些直接参与治疗考虑移植的终末期肾病患者的人,以降低目前阻碍这些患者长期预后的心血管事件的发生率nts。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A new risk score model to predict the presence of significant coronary artery disease in renal transplant candidates.

A new risk score model to predict the presence of significant coronary artery disease in renal transplant candidates.

A new risk score model to predict the presence of significant coronary artery disease in renal transplant candidates.

A new risk score model to predict the presence of significant coronary artery disease in renal transplant candidates.

Background: Renal transplant candidates are at high risk of coronary artery disease (CAD). We sought to develop a new risk score model to determine the pre-test probability of the occurrence of significant CAD in renal transplant candidates.

Methods: A total of 1,060 renal transplant candidates underwent a comprehensive cardiovascular risk evaluation. Patients considered at high risk of CAD (age ≥50 years, with either diabetes mellitus (DM) or cardiovascular disease (CVD)), or having noninvasive testing suggestive of CAD were referred for coronary angiography (n = 524). Significant CAD was defined by the presence of luminal stenosis ≥70%. A binary logistic regression model was built, and the resulting logistic regression coefficient B for each variable was multiplied by 10 and rounded to the next whole number. For each patient, a corresponding risk score was calculated and the receiver operating characteristic (ROC) curve was constructed.

Results: The final equation for the model was risk score = (age × 0.4) + (DM × 9) + (CVD × 14) and for the probability of CAD (%) = (risk score × 2) - 23. The corresponding ROC for the accuracy of the diagnosis of CAD was 0.75 (P <0.0001) in the developmental model.

Conclusions: We developed a simple clinical risk score to determine the pre-test probability of significant CAD in renal transplant candidates. This model may help those directly involved in the care of patients with end-stage renal disease being considered for transplantation in an attempt to reduce the rate of cardiovascular events that presently hampers the long-term prognosis of such patients.

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