Nomogram to Estimate the Risk of Chronic Kidney Disease-Associated Pruritus in Patients with End-Stage Renal Disease Undergoing Peritoneal Dialysis: Model Development and Validation Study

被引:0
|
作者
Gu, Wen [1 ,2 ]
Zhang, Ming [1 ]
Liang, Changna [2 ]
Ma, Shaohui [1 ]
Wang, Xiaopei [2 ]
Yuan, Huijie [1 ]
Luo, Zhaoyao [1 ]
Lv, Jing [2 ]
机构
[1] Xi An Jiao Tong Univ, Dept Med Imaging, Affiliated Hosp 1, Xian, Peoples R China
[2] Xi An Jiao Tong Univ, Kidney Hosp, Dept Nephrol, Affiliated Hosp 1, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
End-stage renal disease; Chronic kidney disease-associated pruritus; Nomogram; Peritoneal dialysis; Interleukin-6; UREMIC PRURITUS; PLASMA HISTAMINE; HEMODIALYSIS; INFLAMMATION; OUTCOMES; INVENTORY;
D O I
10.1159/000539786
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Chronic kidney disease-associated pruritus (CKD-aP) frequently occurs in patients with end-stage renal disease (ESRD) undergoing peritoneal dialysis (PD) and presents a therapeutic challenge to physicians owing to the diversity of its pathogenesis. Herein, we developed and validated a nomogram model for individualized risk estimation of CKD-aP and investigated the possible causes of CKD-aP in PD patients. Methods: We retrospectively screened patients with CKD-aP who underwent PD between 2021 and 2023 at the First Affiliated Hospital of Xi'an Jiaotong University Peritoneal Dialysis Center. Nomograms for each outcome were computed from multivariate logistic regression models with the least absolute shrinkage and selection operator regression and univariate logistic regression for variable selection. The discriminative ability was estimated by Harrell's C-index, and the accuracy was assessed graphically with a calibration curve plot. Models were validated internally using bootstrapping and externally by calculating their performance on a validation cohort. Decision curve analysis was used to assess the model's clinical usefulness. Results: In all, a total of 487 patients were entered in the analysis, including 325 in the development cohort and 162 in the validation cohort. The final nomogram incorporated five variables: age, interleukin-6, hemoglobin, residual urine volume, and renal Kt/V. The C-index of the model was 0.733 (95% CI: 0.679-0.787), and the calibration curve was a straight line with a slope close to 1. Both internal and external validations confirmed the model's good performance, with C-index of 0.725 (95% CI: 0.662-0.774) and 0.706 (95% CI: 0.623-0.789), respectively. Decision curve analysis showed that the nomogram had good clinical benefits. Conclusion: Our study proposes a nomogram model for CKD-aP risk assessment in ESRD patients with PD. This nomogram might help in clinical decision-making and evidence-based selection of therapy. We conducted a study to better understand and predict the risk of CKD-associated pruritus, a common itching condition in patients with severe kidney disease undergoing peritoneal dialysis. Our research included an analysis of the risk factors associated with this condition. Using information from uremic pruritus patients, we developed a special tool that takes into account factors such as a patient's age, certain blood markers, hemoglobin levels, residual urine volume, and renal Kt/V. This tool is designed to help doctors estimate a patient's likelihood of developing CKD-associated pruritus. Our results show that this tool is not only accurate but also practical for use in medical settings, aiding doctors in making informed treatment decisions.
引用
收藏
页码:755 / 767
页数:13
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