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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

机译:慢性肾脏病患者的药物使用方式和多药负担:德国慢性肾脏病研究

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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?msup2/sup or an eGFR ≥60?mL/min/1.73msup2/sup 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.
机译:背景患有慢性肾脏疾病(CKD)的患者承担着大量合并症,导致多种药物的处方和多药风险。但是,有关该人群药物使用的数据很少。方法共有5217名成年人的肾小球滤过率(eGFR)估计在30至60?mL / min / 1.73?m 2 或eGFR≥60?mL / min / 1.73m 研究了2 和明显的蛋白尿(> 500?mg /天)。在基线期(2010-12年)和随访4年(FU)后,对当前使用药物的自我报告数据进行了评估。使用多变量Logistic回归评估与多元药房(定义为每天常规使用五种或更多药物)以及起始或终止多元药房相关的患病率和风险因素。结果在基线和FU时,多药房的患病率接近80%,从CKD G1期患者的62%到CKD G3b期患者的86%。每天服用不同药物的中位数为八(范围为0-27)。最常使用β受体阻滞剂,血管紧张素转化酶抑制剂和他汀类药物。 CKD G分期,年龄和体重指数,糖尿病,心血管疾病和吸烟史的增加与FU期间多药房的流行及其维持密切相关。糖尿病也与多药业的启动显着相关[赔率(OR)2.46,(95%置信区间1.36-4.45); P≥0.003]。结论CKD患者的用药负担较高。似乎有必要进行进一步的研究,以解决这种弱势患者群体中多药店的影响,药物相互作用的风险以及降低风险的策略。

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