Department of Internal Medicine, Medical School Hannover, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.
Curr Pharm Biotechnol. 2011 Dec;12(12):2015-9. doi: 10.2174/138920111798808275.
On September 11, 1945 Maria Schafstaat was the first patient who successfully underwent a dialysis treatment for acute kidney injury (AKI), formerly known as acute renal failure. Since then, the number of patients with AKI is increasing worldwide. Today AKI is generally one feature of a multiple organ dysfunction syndrome (MODS), which develops in response to major surgery, cardiogenic shock or sepsis. Several clinical studies have shown that early and appropriate antibiotic therapy in those patients is of utter importance, yet it remains one of the most difficult challenges to meet. Even in critically ill patients with conserved renal function a myriad of pathophysiological changes, resulting in increased volume of distribution, decreased protein binding and altered hepatic drug clearance, makes appropriate antibiotic dosin difficult. Adequate pharmacotherapy, i.e. dose of anti-infective agens is becoming even more complicated if it has to be tailored to counteract their removal by different modes and intensities of renal replacement therapy. This review summarizes our sparse knowledge about pharmacokinetic studies and dosing recommendations of drugs in patients with AKI undergoing continuous renal replacement therapies (CRRTs) such as continuous venovenous hemofiltration (CVVH) as well as extended dialysis (ED), an increasingly used method to treat patients with AKI in the intensive care setting. We reflect on failure of several large prospective controlled studies to show a survival benefit of higher doses of renal replacement therapy, a finding that might be caused by the fact that we still adhere to dosing guidelines for antibiotics which are at best ineffectual but might also lead to potentially dangerous underdosing of these life saving drugs. Lastly we address possible strategies to overcome the lack of knowledge, the lack of data and the lack of interest in this important area of critical care medicine. Improvement of clinical outcomes and reduction of antibiotic resistance in this patient population will require nephrologist, intensivists and pharmacists to work together.
1945 年 9 月 11 日,Maria Schafstaat 是首位成功接受透析治疗急性肾损伤(AKI)的患者,AKI 以前称为急性肾衰竭。从那时起,全世界 AKI 患者的数量一直在增加。如今,AKI 通常是多器官功能障碍综合征(MODS)的一个特征,MODS 是对大手术、心源性休克或败血症的反应。几项临床研究表明,早期和适当的抗生素治疗对这些患者至关重要,但这仍然是最难满足的挑战之一。即使在肾功能正常的危重症患者中,由于分布容积增加、蛋白结合减少和肝药物清除改变等多种病理生理变化,也使得抗生素剂量难以确定。如果必须通过不同模式和强度的肾脏替代疗法来调整抗生素剂量以抵消其清除,那么适当的药物治疗(即抗感染药物的剂量)就变得更加复杂。本文综述了我们对接受连续肾脏替代治疗(如连续静脉-静脉血液滤过(CVVH)和扩展透析(ED))的 AKI 患者的药物药代动力学研究和剂量建议的有限认识。我们反思了几项大型前瞻性对照研究未能显示更高剂量肾脏替代治疗的生存获益,这一发现可能是由于我们仍然坚持使用抗生素剂量指南,这些指南要么无效,要么可能导致这些救命药物潜在危险的剂量不足。最后,我们探讨了克服这一重要重症监护医学领域缺乏知识、数据和关注的可能策略。改善该患者群体的临床结局和减少抗生素耐药性需要肾脏病专家、重症监护专家和药剂师共同努力。