Paterson David L
University of Queensland, Clinical Research Centre, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
Clin Infect Dis. 2008 Sep 15;47 Suppl 1:S14-20. doi: 10.1086/590062.
Serious infections with gram-negative pathogens continue to be associated with considerable mortality. Increasing antibiotic resistance in organisms such as Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae is contributing to difficulties with choosing antibiotics to prescribe for these infections. Optimization of therapy against these organisms starts with the initial empirical antibiotic choice. Surveillance data and hospital or unit antibiograms may inform this decision, although individualization of the initial regimen on the basis of prior antibiotic use and prior isolation of resistant pathogens may be more important. Combinations of antibiotics are often required empirically, and "combination antibiograms" may need to be developed for this purpose. Preliminary data suggest that extending the time over which a dose of antipseudomonal beta-lactam antibiotics is infused may improve clinical outcomes; however, this idea remains to be confirmed in randomized trials. The role of direct susceptibility testing in aiding more-rapid initiation of appropriate antibiotic therapy is also being studied. When identification and susceptibility testing is complete, the antibiotic regimen for infections due to gram-negative pathogens can be "fine tuned." On some occasions, this fine tuning necessitates the introduction of "salvage" antibiotics, such as colistin or tigecycline; on others, it necessitates de-escalation and early termination of therapy. The lack of new antibiotic options against gram-negative pathogens underscores the need for optimization of current therapies and prevention of the spread of these organisms.
革兰氏阴性病原体引起的严重感染仍然与相当高的死亡率相关。铜绿假单胞菌、鲍曼不动杆菌和肺炎克雷伯菌等微生物的抗生素耐药性不断增加,这给选择用于治疗这些感染的抗生素带来了困难。针对这些微生物的治疗优化始于最初的经验性抗生素选择。监测数据以及医院或科室的抗菌谱图可为这一决策提供参考,不过,根据先前的抗生素使用情况和先前分离出的耐药病原体对初始治疗方案进行个体化调整可能更为重要。经验性治疗通常需要联合使用抗生素,为此可能需要制定“联合抗菌谱图”。初步数据表明,延长抗假单胞菌β-内酰胺类抗生素的输注时间可能会改善临床结局;然而,这一观点仍有待在随机试验中得到证实。直接药敏试验在帮助更快开始适当抗生素治疗方面的作用也正在研究中。当鉴定和药敏试验完成后,针对革兰氏阴性病原体感染的抗生素治疗方案可以进行“微调”。在某些情况下,这种微调需要引入“挽救性”抗生素,如黏菌素或替加环素;在其他情况下,则需要降阶梯治疗并提前终止治疗。针对革兰氏阴性病原体缺乏新的抗生素选择凸显了优化当前治疗方法以及预防这些微生物传播的必要性。