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Development of a nomogram for predicting hyperkalemia in advanced chronic kidney disease
Jonathan S Chávez-Iñiguez1,2, R Lizzete Ornelas-Ruvalcaba1,2, Gonzalo Rodríguez-García1
1Nephrology Department, Hospital Civil de Guadalajara Fray Antonio Alcalde, Guadalajara, Jalisco, Mexico.
Insights
Predicting hyperkalemia (HyperK) in advanced chronic kidney disease (CKD) is difficult. New sex-specific nomograms accurately identify low-risk patients, enabling personalized outpatient nephrology care and reducing intensive monitoring needs.
Area of Science:
- Nephrology
- Internal Medicine
- Clinical Prediction Models
Background:
- Hyperkalemia (HyperK) is a serious complication in advanced chronic kidney disease (CKD).
- Predicting HyperK in outpatient settings is challenging.
- Current risk stratification methods lack precision for individualized care.
Purpose of the Study:
- To identify independent predictors of HyperK in advanced CKD patients.
- To develop and validate sex-specific nomograms for HyperK risk prediction.
- To support personalized management strategies in outpatient nephrology.
Main Methods:
- Retrospective cohort study of 395 patients with CKD stages 4-5.
- Logistic regression with LASSO selection for predictor identification.
- Development and validation of sex-specific nomograms using AUROC and calibration plots.
Main Results:
- 76% of patients developed HyperK during follow-up.
- Predictors included higher creatinine, calcium, age; lower risk with higher sodium, hemoglobin, obesity, thiazides.
- Sex-specific nomograms showed good discrimination (AUROC 0.78 men, 0.81 women) and high negative predictive value (>95%).
Conclusions:
- Validated, sex-specific nomograms enable accurate, individualized HyperK risk prediction in advanced CKD.
- These tools can identify low-risk patients, potentially reducing intensive monitoring.
- Findings support personalized management in outpatient nephrology settings.
Abstract:
Hyperkalemia (HyperK) is a potentially life-threatening complication in advanced chronic kidney disease (CKD), yet its prediction in real-world outpatient settings remains challenging. In a retrospective cohort study including 395 patients with CKD stages 4-5, all with baseline serum potassium levels within the normal range, followed for up to 2.2 years. Clinical, biochemical, and pharmacological variables were obtained from electronic health records, and logistic regression with LASSO selection was applied to identify independent predictors of HyperK. Sex-stratified nomograms were developed to facilitate individualized risk estimation, and model performance was assessed using AUROC, calibration plots, and internal validation with 1,000 bootstrap resamples. During follow-up, 303 patients (76%) developed HyperK. Independent predictors included higher serum creatinine, calcium, and age, while higher sodium levels, hemoglobin, obesity, and thiazide use were associated with lower risk. In adjusted models, men had a 49% lower risk of HyperK (OR 0.51, 95% CI 0.28-0.92). Sex-specific nomograms demonstrated good discrimination, with AUROC of 0.78 in men and 0.81 in women, and calibration analyses confirmed adequate model fit. Importantly, both models showed a high negative predictive value (>95%), supporting their use in safely identifying low-risk patients who may require less intensive monitoring. Secondary analyses showed that higher phosphate was independently associated with mortality (OR 1.74, 95% CI 1.04-2.93), while increased creatinine predicted the need for kidney replacement therapy (OR 1.29, 95% CI 1.08-1.56). These findings provide validated, sex-specific nomograms that enable individualized risk prediction of HyperK in advanced CKD, supporting personalized management in outpatient nephrology care.
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