预测非心脏手术肾衰竭患者术后心脏事件和死亡率:一项外部验证研究。

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Kidney360 Pub Date : 2025-04-09 DOI:10.34067/KID.0000000811
Gurpreet S Pabla, Navdeep Tangri, Reid H Whitlock, Thomas Ferguson, Tyrone G Harrison
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引用次数: 0

摘要

背景:接受非心脏手术的肾衰竭患者发生心脏不良事件和死亡的风险很高,然而现有的围手术期风险预测工具在这些患者中并不有效。最近,从加拿大阿尔伯塔的一个肾衰竭队列中开发了三个模型。在这项研究中,我们在加拿大马尼托巴省的肾衰竭手术队列中评估了这些阿尔伯塔模型。方法:该队列包括来自加拿大马尼托巴省的成年人(≥18岁),既往存在肾衰竭(估计肾小球滤过率< 15 mL/min/1.73m2或接受维护性透析),2007-2019年期间接受非心脏手术。主要结局是30天内急性心肌梗死、心脏骤停、室性心律失常和全因死亡率的综合结果。这三个模型包括越来越多的变量:人口统计学和手术特征(模型1)、合并症(模型2)和术前白蛋白和血红蛋白(模型3)。使用受试者工作特征曲线下面积(AUC-ROC)、校准和马尼托巴数据的Brier评分来评估模型的性能。通过对所有三个模型应用阿尔伯塔模型系数来预测马尼托巴数据的结果,以及对马尼托巴数据使用逻辑回归重新估计阿尔伯塔模型预测系数,对这一点进行了评估。结果:我们在4175名参与者中进行了12082次手术;共观察到569个结局(4.7%)。这三个模型在两种方法下都表现良好,使用具有Alberta系数的模型,AUC-ROC范围为0.821(模型1)至0.874(模型3)。模型1、2和3的校正斜率分别为1.32、1.40和1.24。改装后,AUC-ROC范围为0.830(模型1)~ 0.861(模型3)。所有重新估计的模型的校准斜率近似为1。在所有原始和重新估计的模型中,Brier分数仍< 0.1。结论:我们的外部验证研究证实,在加拿大艾伯塔省开发的肾衰竭特异性术后结局模型在地理上不同的加拿大人群中表现良好。未来的研究应该探索这些模型在不同环境下的表现,并评估其临床效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting Postoperative Cardiac Events and Mortality for People with Kidney Failure Having Non-Cardiac Surgery: An External Validation Study.

Background: Patients with kidney failure undergoing non-cardiac surgery are at high risk of adverse cardiac events and mortality, however existing perioperative risk prediction tools for these outcomes are not valid in these patients. Recently, three models were developed from a kidney failure cohort in Alberta, Canada. In this study, we evaluated these Alberta models in a kidney failure cohort that had surgery in Manitoba, Canada.

Methods: The cohort included adults from Manitoba, Canada (≥ 18 years) with pre-existing kidney failure (estimated glomerular filtration rate < 15 mL/min/1.73m2 or receiving maintenance dialysis) undergoing non-cardiac surgeries between 2007-2019. The primary outcome was a composite of acute myocardial infarction, cardiac arrest, ventricular arrhythmia, and all-cause mortality within 30 days. The three models included an increasing number of variables: demographics and surgical characteristics (model 1), comorbidities (model 2), and preoperative albumin and hemoglobin (model 3). Model performance was evaluated using Area Under the Receiver Operating Characteristic Curve (AUC-ROC), calibration, and Brier score on Manitoba data. This was evaluated by applying Alberta model coefficients for all three models to predict outcomes on Manitoba data, and also by re-estimating the Alberta model predictor coefficients using logistic regression on Manitoba data.

Results: We identified 12,082 surgeries performed in 4,175 participants; 569 outcomes were observed (4.7%). All three models performed well with both approaches, with AUC-ROC ranging from 0.821 (model 1) to 0.874 (model 3) using the models with Alberta coefficients. Calibration slopes were 1.32, 1.40, and 1.24 for models 1, 2, and 3, respectively. Upon refitting, AUC-ROC ranged from 0.830 (model 1) to 0.861 (model 3). Calibration slopes approximated 1 across all the re-estimated models. Brier scores remained < 0.1 across all original and re-estimated models.

Conclusions: Our external validation study confirmed that the kidney failure specific postoperative outcome models developed in Alberta, Canada, performed well in a geographically distinct Canadian population. Future research should explore the performance of these models in different settings and evaluate their clinical impact with prospective implementation.

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Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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