Hyperpolypharmacy in patients with chronic kidney disease and its impact on clinical outcomes

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Authors: Agathe Mouheb, Marie Metzger, Natalia Alencar de Pinho, Christian Jacquelinet, Maurice Laville, Ziad A Massy, Sophie Liabeuf, Solène M. Laville, CKD-REIN STUDY GROUP, Dorothée Cannet, Christian Combe, Denis Fouque
+59 more Luc Frimat, Aghilès Hamroun, Yves-Édouard Herpe, Oriane Lambert, Céline Lange, Pascal Morel, Christophe Pascal, Roberto Pecoits-Filho, Joost Schantsra, Bénédicte Stengel, Investigators, T. Hannedouche, B. Moulin, A. Klein, C. Combe, J. P. Bourdenx, A. Keller, C. Delclaux, B. Vendrely, B. Deroure, A. Lacraz, T. Lobbedez, I. Landru, Z. Massy, P. Lang, X. Belenfant, E. Thervet, P. Urena, M. Delahousse, C. Vela, M. Essig, D. Clément, H. Sekhri, M. Smati, M. Jamali, B. Hacq, V. Panescu, M. Bellou, Luc Frimat, N. Kamar, C. Noël, F. Glowacki, N. Maisonneuve, R. Azar, M. Hoffmann, M. Hourmant, A. Testa, D. Besnier, G. Choukroun, G. Lambrey, S. Burtey, G. Lebrun, E. Magnant, M. Laville, D. Fouque, L. Juillard, C. Chazot, P. Zaoui, F. Kuentz
Cited by: 1
References: 28

Abstract

Hyperpolypharmacy (≥ 10 daily medications) is frequent in patients with chronic kidney disease (CKD), but its impact remains poorly characterized. This study, based on 3,011 non-dialyzed, non-transplant CKD outpatients from the CKD-REIN cohort (eGFR < 60 mL/min/1.73 m 2 ) aimed to describe drug burden and assess associations between hyperpolypharmacy and adverse outcomes. Drug prescription, kidney function, adverse drug reactions (ADRs), hospitalizations, kidney replacement therapy and deaths before KRT were prospectively recorded over five years. Median age was 69 years and mean eGFR was 34 mL/min/1.73 m 2 . At baseline, 80% of the cohort had polypharmacy (≥ 5 daily medications), and 33% had hyperpolypharmacy. These rates remained stable over time. Diabetes, dyslipidemia, and a history of cardiovascular and respiratory diseases were the main contributors to hyperpolypharmacy status. Hyperpolypharmacy was associated with greater likelihoods of an ADR (hazard ratio (HR) [95% confidence interval (CI)] 1.21 [1.04–1.40]), hospitalization (HR [95%CI] 1.34 [1.18–1.51]) and death before KRT (HR [95%CI] 1.46 [1.17–1.82]). Among patients with eGFR ≥ 30 mL/min/1.73m 2 , hyperpolypharmacy also raised the risk of KRT initiation (HR [95%CI] 1.46 [1.00–2.13]), but not in those with eGFR < 30 (HR [95%CI] 0.94 [0.78–1.14]). These results identify hyperpolypharmacy as a significant concern in CKD and underscore the importance of regular medication reviews to reduce adverse outcomes.

Fields of Study & Subjects

Diabetes Treatment and Management Heart Failure Treatment and Management Chronic Kidney Disease and Diabetes

Publication details

Journal / source
Scientific Reports
Publisher
Springer Science and Business Media LLC
Volume
16
Issue
1
Pages
2653–2653
Publication date
20 January 2026
Language
EN