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首页> 外文期刊>Advances in chronic kidney disease >Drug Disposition Issues in CKD: Implications for Drug Discovery and Regulatory Approval
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Drug Disposition Issues in CKD: Implications for Drug Discovery and Regulatory Approval

机译:CKD中的药物处置问题:对药物发现和监管批准的影响

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摘要

Patients with chronic kidney disease (CKD) have several comorbidities that require pharmacologic intervention including hypertension, diabetes, anemia, and cardiovascular disease. Advanced CKD patients (eg, treated with hemodialysis) take an average of 12 medications concurrently and are known to suffer from an increased number of medication-related adverse drug events. Recent basic and clinical research has identified altered renal and nonrenal drug clearance in CKD as one mediator of the increased adverse drug events observed in this patient population. This review will briefly describe pharmacokinetic considerations in CKD, review the Food and Drug Administration guidelines for performing pharmacokinetic studies in CKD patients, and outline the roles of academia, industry, and regulatory agencies in improving drug safety in CKD patients. (C) 2016 by the National Kidney Foundation, Inc. All rights reserved.
机译:患有慢性肾脏疾病(CKD)的患者有几种合并症需要药物干预,包括高血压,糖尿病,贫血和心血管疾病。晚期CKD患者(例如接受血液透析治疗的患者)平均同时服用12种药物,并且已知患有与药物相关的不良药物事件数量增加。最近的基础和临床研究已经确定,CKD中肾脏和非肾脏药物清除率的改变是该患者人群中不良药物事件增加的一种媒介。这篇综述将简要描述CKD中的药代动力学注意事项,回顾食品和药物管理局在CKD患者中进行药代动力学研究的指南,并概述学术界,行业和监管机构在改善CKD患者的药物安全性中的作用。 (C)美国国家肾脏基金会,2016年。保留所有权利。

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