Bassetti Matteo, Peghin Maddalena, Vena Antonio, Giacobbe Daniele Roberto
Clinica Malattie Infettive, Azienda Sanitaria Universitaria Integrata di Udine, Presidio Ospedaliero Universitario Santa Maria della Misericordia, Udine, Italy.
Department of Health Sciences, University of Genoa, Genoa, Italy.
Front Med (Lausanne). 2019 Apr 16;6:74. doi: 10.3389/fmed.2019.00074. eCollection 2019.
The treatment of multidrug-resistant Gram-negative bacteria (MDR-GNB) infections in critically ill patients presents many challenges. Since an effective treatment should be administered as soon as possible, resistance to many antimicrobial classes almost invariably reduces the probability of adequate empirical coverage, with possible unfavorable consequences. In this light, readily available patient's medical history and updated information about the local microbiological epidemiology remain critical for defining the baseline risk of MDR-GNB infections and firmly guiding empirical treatment choices, with the aim of avoiding both undertreatment and overtreatment. Rapid diagnostics and efficient laboratory workflows are also of paramount importance both for anticipating diagnosis and for rapidly narrowing the antimicrobial spectrum, with de-escalation purposes and in line with antimicrobial stewardship principles. Carbapenem-resistant Enterobacteriaceae, , and are being reported with increasing frequencies worldwide, although with important variability across regions, hospitals and even single wards. In the past few years, new treatment options, such as ceftazidime/avibactam, meropenem/vaborbactam, ceftolozane/tazobactam, plazomicin, and eravacycline have become available, and others will become soon, which have provided some much-awaited resources for effectively counteracting severe infections due to these organisms. However, their optimal use should be guaranteed in the long term, for delaying as much as possible the emergence and diffusion of resistance to novel agents. Despite important progresses, pharmacokinetic/pharmacodynamic optimization of dosages and treatment duration in critically ill patients has still some areas of uncertainty requiring further study, that should take into account also resistance selection as a major endpoint. Treatment of severe MDR-GNB infections in critically ill patients in the near future will require an expert and complex clinical reasoning, of course taking into account the peculiar characteristics of the target population, but also the need for adequate empirical coverage and the more and more specific enzyme-level activity of novel antimicrobials with respect to the different resistance mechanisms of MDR-GNB.
治疗重症患者的多重耐药革兰氏阴性菌(MDR - GNB)感染面临诸多挑战。由于应尽快给予有效治疗,对多种抗菌药物类别产生耐药性几乎总会降低充分经验性覆盖的可能性,并可能带来不良后果。有鉴于此, readily available patient's medical history(此处“readily available”表述有误,应是“patient's readily available medical history”,即患者现成的病史)和有关当地微生物流行病学的最新信息对于确定MDR - GNB感染的基线风险以及坚定地指导经验性治疗选择至关重要,目的是避免治疗不足和过度治疗。快速诊断和高效的实验室工作流程对于预期诊断以及迅速缩小抗菌谱也至关重要,这符合降阶梯治疗目的且符合抗菌药物管理原则。耐碳青霉烯类肠杆菌科细菌在全球范围内的报告频率日益增加,尽管在不同地区、医院甚至单个病房存在重要差异。在过去几年中,新的治疗选择,如头孢他啶/阿维巴坦、美罗培南/瓦博巴坦、头孢洛扎/他唑巴坦、普拉佐米星和依拉环素已可供使用,其他药物也将很快上市,这些为有效应对由这些微生物引起的严重感染提供了一些期待已久的资源。然而,从长远来看,应保证它们的最佳使用,以尽可能延迟对新型药物耐药性的出现和传播。尽管取得了重要进展,但重症患者剂量和治疗持续时间的药代动力学/药效学优化仍存在一些需要进一步研究的不确定领域,这也应将耐药性选择作为主要终点考虑在内。在不久的将来,治疗重症患者的严重MDR - GNB感染将需要专业且复杂的临床推理,当然要考虑目标人群的特殊特征,还要考虑充分经验性覆盖的必要性以及新型抗菌药物针对MDR - GNB不同耐药机制的越来越具体的酶水平活性。