College of Pharmacy, University of Rhode Island, Kingston, RI, USA.
Westchester Medical Center, New York Medical College, Valhalla, NY, USA.
Ann Med. 2022 Dec;54(1):1686-1700. doi: 10.1080/07853890.2022.2085881.
The progressive increase in antibiotic resistance in recent decades calls for urgent development of new antibiotics and antibiotic stewardship programs to help select appropriate treatments with the goal of minimising further emergence of resistance and to optimise clinical outcomes. Three new tetracycline-class antibiotics, eravacycline, omadacycline, and tigecycline, have been approved within the past 15 years, and represent a new era in the use of tetracyclines. These drugs overcome the two main mechanisms of acquired tetracycline-class resistance and exhibit a broad spectrum of activity against gram-positive, gram-negative, anaerobic, and atypical pathogens, including many drug-resistant strains. We provide an overview of the three generations of tetracycline-class drugs, focussing on the efficacy, safety, and clinical utility of these three new third-generation tetracycline-class drugs. We also consider various scenarios of unmet clinical needs where patients might benefit from re-engagement with tetracycline-class antibiotics including outpatient treatment options, patients with known β-lactam antibiotic allergy, reducing the risk of infection, and their potential as monotherapy in polymicrobial infections while minimising the risk of any potential drug-drug interaction. KEY MESSAGESThe long-standing safety profile and broad spectrum of activity of tetracycline-class antibiotics made them a popular choice for treatment of various bacterial infections; unfortunately, antimicrobial resistance has limited the utility of the early-generation tetracycline agents.The latest generation of tetracycline-class antibiotics, including eravacycline, tigecycline, and omadacycline, overcomes the most common acquired tetracycline resistance mechanisms.Based on characteristics and clinical data, these newer tetracycline agents provide an effective antibiotic option in the treatment of approved indications in patients with unmet clinical needs - including patients with severe penicillin allergy, with renal or hepatic insufficiency, recent infection, or polymicrobial infections, and those at risk of drug-drug interactions.
近年来,抗生素耐药性的逐渐增加要求紧急开发新的抗生素和抗生素管理计划,以帮助选择合适的治疗方法,最大限度地减少进一步出现耐药性,并优化临床结果。在过去的 15 年中,有三种新的四环素类抗生素——依拉环素、奥马环素和替加环素获得批准,这代表了四环素类药物使用的新时代。这些药物克服了获得性四环素类耐药的两个主要机制,具有广泛的活性,可对抗革兰氏阳性、革兰氏阴性、厌氧和非典型病原体,包括许多耐药菌株。我们概述了三代四环素类药物,重点介绍了这三种新的第三代四环素类药物的疗效、安全性和临床实用性。我们还考虑了各种未满足的临床需求场景,在这些场景中,患者可能会从重新使用四环素类抗生素中受益,包括门诊治疗选择、已知对β-内酰胺类抗生素过敏的患者、降低感染风险,以及它们在混合感染中作为单一疗法的潜力,同时最大限度地降低任何潜在药物相互作用的风险。
四环素类抗生素的长期安全特性和广泛的活性使其成为治疗各种细菌感染的首选药物;不幸的是,抗菌耐药性限制了早期一代四环素类药物的应用。
最新一代的四环素类抗生素,包括依拉环素、替加环素和奥马环素,克服了最常见的获得性四环素耐药机制。
基于特性和临床数据,这些新型四环素类药物为有未满足临床需求的患者(包括严重青霉素过敏、肾功能或肝功能不全、近期感染或混合感染以及有药物相互作用风险的患者)提供了有效的抗生素治疗选择,可用于治疗批准的适应证。