Patterns of medication use and the burden of polypharmacy in patients with chronic kidney disease: the German Chronic Kidney Disease study

Author:

Schmidt Insa M1,Hübner Silvia2,Nadal Jennifer3,Titze Stephanie2,Schmid Matthias3,Bärthlein Barbara45,Schlieper Georg6ORCID,Dienemann Thomas2,Schultheiss Ulla T7,Meiselbach Heike2,Köttgen Anna7,Flöge Jürgen6,Busch Martin8,Kreutz Reinhold1,Kielstein Jan T9ORCID,Eckardt Kai-Uwe210

Affiliation:

1. Department of Clinical Pharmacology and Toxicology, Charité–Universitätsmedizin Berlin, Berlin, Germany

2. Department of Nephrology and Hypertension, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany

3. Department of Medical Biometry, Informatics, and Epidemiology, University Hospital, Bonn, Germany

4. Department of Medical Informatics, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany

5. Medical Centre for Information and Communication Technology, University Hospital Erlangen, Erlangen, Germany

6. Division of Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany

7. Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center-University of Freiburg, Freiburg, Germany

8. Department of Internal Medicine III, University Hospital Jena, Jena, Germany

9. Medical Clinic V – Nephrology, Rheumatology, Blood Purification, Academic Teaching Hospital Braunschweig, Braunschweig, Germany

10. Department of Nephrology and Medical Intensive Care, Charité–Universitätsmedizin Berlin, Berlin, Germany

Abstract

Abstract Background Patients with chronic kidney disease (CKD) bear a substantial burden of comorbidities leading to the prescription of multiple drugs and a risk of polypharmacy. However, data on medication use in this population are scarce. Methods A total of 5217 adults with an estimated glomerular filtration rate (eGFR) between 30 and 60 mL/min/1.73 m2 or an eGFR ≥60 mL/min/1.73m2 and overt proteinuria (>500 mg/day) were studied. Self-reported data on current medication use were assessed at baseline (2010–12) and after 4 years of follow-up (FU). Prevalence and risk factors associated with polypharmacy (defined as the regular use of five or more drugs per day) as well as initiation or termination of polypharmacy were evaluated using multivariable logistic regression. Results The prevalence of polypharmacy at baseline and FU was almost 80%, ranging from 62% in patients with CKD Stage G1 to 86% in those with CKD Stage G3b. The median number of different medications taken per day was eight (range 0–27). β-blockers, angiotensin-converting enzyme inhibitors and statins were most frequently used. Increasing CKD G stage, age and body mass index, diabetes mellitus, cardiovascular disease and a history of smoking were significantly associated with both the prevalence of polypharmacy and its maintenance during FU. Diabetes mellitus was also significantly associated with the initiation of polypharmacy [odds ratio (OR) 2.46, (95% confidence interval 1.36–4.45); P = 0.003]. Conclusion Medication burden in CKD patients is high. Further research appears warranted to address the implications of polypharmacy, risks of drug interactions and strategies for risk reduction in this vulnerable patient population.

Funder

German Ministry of Education and Research

KfH Foundation for Preventive Medicine

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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