Nation Roger L, Rigatto Maria Helena P, Falci Diego R, Zavascki Alexandre P
Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville 3052, Australia.
Infectious Diseases Service, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre 90035-903, Brazil.
Antibiotics (Basel). 2019 Mar 14;8(1):24. doi: 10.3390/antibiotics8010024.
Polymyxins are valuable antimicrobials for the management of multidrug-resistant Gram-negative bacteria; however, nephrotoxicity associated with these drugs is a very common side effect that occurs during treatment. This article briefly reviews nephrotoxic mechanisms and risk factors for polymyxin-associated acute kidney injury (AKI) and discusses dosing strategies that may mitigate kidney damage without compromising antimicrobial activity. Polymyxins have a very narrow therapeutic window and patients requiring treatment with these drugs are frequently severely ill and have multiple comorbidities, which increases the risk of AKI. Notably, there is a significant overlap between therapeutic and toxic plasma polymyxin concentrations that substantially complicates dose selection. Recent dosing protocols for both colistin and polymyxin B have been developed and may help fine tune dose adjustment of these antibiotics. Minimizing exposure to modifiable risk factors, such as other nephrotoxic agents, is strongly recommended. The dose should be carefully selected, particularly in high-risk patients. The administration of oxidative stress-reducing drugs is a promising strategy to ameliorate polymyxin-associated AKI, but still requires support from clinical studies.
多粘菌素是治疗多重耐药革兰氏阴性菌的重要抗菌药物;然而,这些药物相关的肾毒性是治疗期间非常常见的副作用。本文简要回顾了多粘菌素相关急性肾损伤(AKI)的肾毒性机制和危险因素,并讨论了在不影响抗菌活性的情况下减轻肾损伤的给药策略。多粘菌素的治疗窗非常窄,需要使用这些药物治疗的患者通常病情严重且有多种合并症,这增加了发生AKI的风险。值得注意的是,治疗性和毒性血浆多粘菌素浓度之间存在显著重叠,这使得剂量选择变得非常复杂。最近已经制定了针对黏菌素和多粘菌素B的给药方案,可能有助于微调这些抗生素的剂量调整。强烈建议尽量减少接触可改变的危险因素,如其他肾毒性药物。应谨慎选择剂量,尤其是在高危患者中。使用减轻氧化应激的药物是改善多粘菌素相关AKI的一种有前景的策略,但仍需要临床研究的支持。