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

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          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 m 2 or an eGFR ≥60 mL/min/1.73m 2 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.

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          Most cited references36

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          Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies.

          To estimate the incidence of serious and fatal adverse drug reactions (ADR) in hospital patients. Four electronic databases were searched from 1966 to 1996. Of 153, we selected 39 prospective studies from US hospitals. Data extracted independently by 2 investigators were analyzed by a random-effects model. To obtain the overall incidence of ADRs in hospitalized patients, we combined the incidence of ADRs occurring while in the hospital plus the incidence of ADRs causing admission to hospital. We excluded errors in drug administration, noncompliance, overdose, drug abuse, therapeutic failures, and possible ADRs. Serious ADRs were defined as those that required hospitalization, were permanently disabling, or resulted in death. The overall incidence of serious ADRs was 6.7% (95% confidence interval [CI], 5.2%-8.2%) and of fatal ADRs was 0.32% (95% CI, 0.23%-0.41%) of hospitalized patients. We estimated that in 1994 overall 2216000 (1721000-2711000) hospitalized patients had serious ADRs and 106000 (76000-137000) had fatal ADRs, making these reactions between the fourth and sixth leading cause of death. The incidence of serious and fatal ADRs in US hospitals was found to be extremely high. While our results must be viewed with circumspection because of heterogeneity among studies and small biases in the samples, these data nevertheless suggest that ADRs represent an important clinical issue.
            • Record: found
            • Abstract: found
            • Article: not found

            Potentially inappropriate medications in the elderly: the PRISCUS list.

            Certain drugs are classified as potentially inappropriate medications (PIM) for the elderly because they carry an increased risk of adverse drug events in this patient group. PIM lists from other countries are of limited usefulness in Germany because different drugs are on the market in each country and prescribing practices vary as well. Thus, a list of potentially inappropriate medications for the elderly was developed specifically for use in Germany. A preliminary PIM list suitable for the German market was created on the basis of a selective literature search and a qualitative analysis of published international PIM lists. The final German PIM list was developed by means of a comprehensive, structured expert survey in two rounds (a so-called Delphi process). 83 drugs in a total of 18 drug classes were rated as potentially inappropriate for elderly patients. For 46 drugs, the experts came to no clear decision after the second Delphi round. For cases in which the administration of a PIM is clinically necessary, the final PRISCUS list contains recommendations for clinical practice, e.g. monitoring of laboratory values and dose adaptation. Therapeutic alternatives are also listed. Potentially inappropriate medications carry the risk of causing adverse drug events in the elderly. A drawback of using a Delphi process to generate a PIM list, as was done for the new German list, is that little scientific evidence is currently available for the evaluation of active substances, potential therapeutic alternatives, and indicated monitoring procedures. Thus, the validity and practicability of the PRISCUS list remain to be demonstrated (and the same holds for PIM lists already published in other countries). It should be used as a component of an overall concept for geriatric pharmacotherapy in which polypharmacy and interacting medications are avoided, and doses are regularly re-evaluated.
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              • Article: not found

              Health outcomes associated with polypharmacy in community-dwelling older adults: a systematic review.

              To summarize evidence regarding the health outcomes associated with polypharmacy, defined as number of prescribed medications, in older community-dwelling persons.

                Author and article information

                Journal
                Clin Kidney J
                Clin Kidney J
                ckj
                Clinical Kidney Journal
                Oxford University Press
                2048-8505
                2048-8513
                October 2019
                24 May 2019
                24 May 2019
                : 12
                : 5
                : 663-672
                Affiliations
                [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
                Author notes
                Correspondence and offprint requests to: Insa M. Schmidt; E-mail: ischmidt1@ 123456bwh.harvard.edu
                Author information
                http://orcid.org/0000-0001-6050-5842
                http://orcid.org/0000-0001-8110-9064
                Article
                sfz046
                10.1093/ckj/sfz046
                6768303
                31584562
                e934207c-605a-4e9b-86d2-c4278357c7a0
                © The Author(s) 2019. Published by Oxford University Press on behalf of ERA-EDTA.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 24 October 2018
                Page count
                Pages: 10
                Funding
                Funded by: German Ministry of Education and Research
                Award ID: FKZ 01ER 0804
                Award ID: 01ER 0818
                Award ID: 01ER 0819
                Award ID: 01ER 0820
                Award ID: 01ER 0821
                Funded by: KfH Foundation for Preventive Medicine
                Categories
                CKD

                Nephrology
                chronic kidney disease,gckd study,medication use,polypharmacy,prescription patterns
                Nephrology
                chronic kidney disease, gckd study, medication use, polypharmacy, prescription patterns

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