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Clinical prediction models for progression of chronic kidney disease to end-stage kidney failure under pre-dialysis nephrology care: results from the Chronic Kidney Disease Japan Cohort Study

机译:慢性肾病进展到透析前肾脏病肾衰竭进展的临床预测模型:慢性肾病日本队列研究结果

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BackgroundReliable prediction tools are needed to identify patients with chronic kidney disease (CKD) at greater risk of developing end-stage kidney failure (ESKF). We developed and validated clinical prediction models (CPMs) for CKD progression to ESKF under pre-dialysis nephrology care using CKD-Japan Cohort (CKD-JAC) data.MethodsWe prospectively followed up 2034 participants with CKD, defined as an estimated glomerular filtration rate (eGFR) less than 60mL/min/1.73m(2), aged 20-75years for a mean of 3.15years. We randomly divided the overall analysis set into development and validation cohorts. In the development cohort, CPMs were developed using Cox proportional hazard regression, and the goodness of fit was evaluated. In the validation cohort, discrimination and calibration of the developed CPMs were evaluated. We also validated developed CPMs in the dataset with the bootstrap method.ResultsESKF onset was observed in 206 and 216 patients in the development (20.3%) and validation (21.2%) cohorts, respectively. Goodness of fit, discrimination, and calibration were worse for a simple model including age, sex, and eGFR than for a complicated model (plus albuminuria, systolic blood pressure, diabetes, serum albumin, and hemoglobin). The mean absolute difference between the observed and predictive probabilities of ESKF onset at 3years was lower for the complicated model than for the simple model (1.57 vs. 1.87%).ConclusionsCPMs employing readily available data could precisely predict progression to ESKF in patients with CKD stage G3a to G5. These developed CPMs may facilitate more appropriate clinical care and shared decision-making between clinicians and patients.
机译:需要应对患有慢性肾病(CKD)的患者进行慢性肾疾病(ESKF)的风险需要核糖预测工具。我们开发和验证了使用CKD-日本队列(CKD-JAC)DATA的透析肾脏护理下对ESKF进行CKD进展的临床预测模型(CPMS)。近期随访2034名与CKD的参与者,定义为估计的肾小球过滤速率( EGFR)小于60毫升/分钟/ 1.73米(2),均为3.15年的平均值为20-75岁。我们随机划分到开发和验证队列的整体分析。在发展队列中,CPMS使用COX比例危险回归开发,评价拟合的良好。在验证队列中,评估开发CPM的歧视和校准。我们还经过验证在数据集中的开发CPMS,并在206日和216名患者中观察到Bootstrap方法。对于包括年龄,性别和egf的简单模型而不是复杂的模型(加上白蛋白尿,收缩压,糖尿病,血清白蛋白和血红蛋白),良好的适应性,歧视和校准更差。复杂模型比简单模型(1.57对1.87%)的复杂模型的观察到和预测性概率之间的平均绝对差异降低g3a到g5。这些已发达的CPM可以促进更适合临床医生和患者之间的共同决策。

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