Weill Cornell Medical College, 1300 York Ave LC-423, New York, NY 10065, USA.
J Clin Pharmacol. 2012 Jan;52(1 Suppl):7S-9S. doi: 10.1177/0091270011413587.
Since the 1960s, systematic studies of drug action in renal failure have found many differences between patients with renal failure and those without. Impaired excretion of drugs was known much earlier and was related to glomerular filtration rate. Kunin first tabulated the pharmacokinetics of antimicrobials and dosage recommendations for azotemic patients in 1967. Other effects of renal failure on drug action include increases in some pathways of drug metabolism with decreases in others and no change in the rest. Some changes in specific drug distribution, drug-protein binding, and drug sensitivity have been demonstrated. This knowledge makes the response of an azotemic patient to a specific dose of a specific drug more predictable than before. This predictability makes drug therapy both safer and more effective for azotemic patients.
自 20 世纪 60 年代以来,对肾衰竭患者药物作用的系统研究发现,肾衰竭患者与非肾衰竭患者之间存在许多差异。更早之前就已经发现药物排泄受损与肾小球滤过率有关。1967 年,Kunin 首次列出了抗菌药物的药代动力学和氮质血症患者的剂量建议。肾衰竭对药物作用的其他影响包括某些药物代谢途径增加,而其他途径减少,其余不变。已经证明了某些特定药物分布、药物-蛋白结合和药物敏感性的变化。这些知识使得氮质血症患者对特定剂量的特定药物的反应比以前更具可预测性。这种可预测性使氮质血症患者的药物治疗更加安全和有效。