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Identifying individuals at risk of needing CKD associated medications in a European kidney disease cohort
Eleni Stamellou1,2, Turgay Saritas3, Marc Froissart4
1Division of Nephrology and Clinical Immunology, RWTH University of Aachen, Aachen, Germany. stamellou.eleni@gmail.com.
Predicting future medication needs in advanced chronic kidney disease (CKD) using patient data can guide treatment decisions. This approach may allow for reduced follow-up frequency for patients with low predicted needs for erythropoiesis-stimulating agents (ESAs) and phosphate binders.
Area of Science:
- Nephrology
- Pharmacotherapy
- Clinical Prediction Models
Background:
- Chronic kidney disease (CKD) management involves various pharmacotherapies.
- Accurate prediction of future medication needs can optimize clinical decision-making and patient follow-up schedules.
Purpose of the Study:
- To identify predictors for the future use of specific pharmacotherapies in patients with advanced CKD (stage G4/G5).
- To assess the potential for these predictions to inform follow-up frequency.
Main Methods:
- A prospective cohort study across six European countries analyzed demographic, comorbidity, hospitalization, laboratory, and mortality data.
- Logistic regression models were used to identify variables predicting the use of vitamin D receptor agonists (VDRA), phosphate binders, erythropoiesis-stimulating agents (ESAs), and iron.
- Model performance was evaluated using C-statistics in derivation and validation cohorts.
Main Results:
- The study included 2196 patients with CKD stage G4/G5.
- Combinations of age, diabetes status, iPTH, calcium, hemoglobin, and serum albumin levels predicted medication use (C-statistics ranging from 0.63 to 0.73).
- Sixteen percent of patients had a predicted likelihood of less than 20% for requiring these medications.
Conclusions:
- Patient characteristics can predict the need for erythropoiesis-stimulating agents (ESAs) and phosphate binders within a two-year period in a multi-country CKD cohort.
- This predictive capability holds potential for reducing follow-up frequency in low-risk CKD patients.
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