Department of Pharmacy, Division of Pediatric Pharmacy, The Johns Hopkins Hospital.
Clin Infect Dis. 2014 May;58(10):1439-48. doi: 10.1093/cid/ciu069. Epub 2014 Feb 5.
Antibiotic resistance in conjunction with the erosion of the drug development pipeline may lead us into a bleak future, a "post-antibiotic era." Because of a shortage of studies addressing treatment options for multidrug-resistant Gram-negative (MDRGN) infections in children, data must be extrapolated from the adult literature. However, even adult studies are limited by significant methodological flaws. We are in urgent need of pediatric specific pharmacokinetic/pharmacodynamic data for agents with activity against MDRGN infections as well as improved clinical outcomes studies. For the time being, we must rely on in vitro studies, observational data, and clinical experience to guide our therapeutic decisions. In this review, we discuss treatment considerations for infections caused by extended-spectrum β-lactamase-producing organisms, AmpC β-lactamase-producing organisms, carbapenem-resistant Enterobacteriaceae, carbapenem-resistant Pseudomonas aeruginosa, and carbapenem-resistant Acinetobacter baumannii in the pediatric population.
抗生素耐药性加上药物研发管道的侵蚀,可能会使我们陷入一个黯淡的未来,即“后抗生素时代”。由于缺乏针对儿童多重耐药革兰氏阴性(MDRGN)感染的治疗选择的研究,数据必须从成人文献中推断出来。然而,即使是成人研究也受到严重方法学缺陷的限制。我们急需针对具有抗 MDRGN 感染活性的药物以及改善临床结果的研究获得儿科特定的药代动力学/药效学数据。目前,我们必须依靠体外研究、观察性数据和临床经验来指导我们的治疗决策。在这篇综述中,我们讨论了在儿科人群中由产生超广谱β-内酰胺酶的生物体、产生 AmpC β-内酰胺酶的生物体、耐碳青霉烯类肠杆菌科、耐碳青霉烯类铜绿假单胞菌和耐碳青霉烯类鲍曼不动杆菌引起的感染的治疗注意事项。