Slama Thomas G
Department of Infectious Diseases, Indiana University School of Medicine, Indianapolis, Indiana 46260, USA.
Crit Care. 2008;12(5):233. doi: 10.1186/cc6994. Epub 2008 Oct 29.
Antipseudomonal carbapenems have played a useful role in our antimicrobial armamentarium for 20 years. However, a review of their use during that period creates concern that their clinical effectiveness is critically dependent on attainment of an appropriate dosing range. Unfortunately, adequate carbapenem dosing is missed for many reasons, including benefit/risk misconceptions, a narrow therapeutic window for imipenem and meropenem (due to an increased rate of seizures at higher doses), increasingly resistant pathogens requiring higher doses than are typically given, and cost containment issues that may limit their use. To improve the use of carbapenems, several initiatives should be considered: increase awareness about appropriate treatment with carbapenems across hospital departments; determine optimal dosing regimens for settings where multidrug resistant organisms are more likely encountered; use of, or combination with, an alternative antimicrobial agent having more favorable pharmacokinetic, pharmacodynamic, or adverse event profile; and administer a newer carbapenem with lower propensity for resistance development (for example, reduced expression of efflux pumps or greater stability against carbapenemases).
抗假单胞菌碳青霉烯类药物在我们的抗菌药物库中已发挥了20年的有益作用。然而,回顾其在此期间的使用情况,令人担忧的是其临床疗效严重依赖于达到适当的给药范围。不幸的是,由于多种原因未能实现碳青霉烯类药物的充分给药,包括对利弊的误解、亚胺培南和美罗培南的治疗窗较窄(因高剂量时癫痫发作率增加)、越来越多的耐药病原体需要比通常给予剂量更高的剂量,以及可能限制其使用的成本控制问题。为改善碳青霉烯类药物的使用,应考虑多项举措:提高医院各科室对碳青霉烯类药物适当治疗的认识;确定在更可能遇到多重耐药菌的环境中的最佳给药方案;使用具有更有利的药代动力学、药效学或不良事件特征的替代抗菌药物或与之联合使用;以及使用耐药性发展倾向较低的新型碳青霉烯类药物(例如,外排泵表达减少或对碳青霉烯酶稳定性更高)。