University of Groningen, University Medical Center Groningen, Department of Clinical Pharmacy and Pharmacology, Groningen, The Netherlands.
National Institute for Public Health and the Environment, National Mycobacteria Reference Laboratory, Bilthoven, The Netherlands.
Antimicrob Agents Chemother. 2019 Jan 29;63(2). doi: 10.1128/AAC.01489-18. Print 2019 Feb.
Multi- and extensively drug-resistant tuberculosis (M/XDR-TB) has become an increasing threat not only in countries where the TB burden is high but also in affluent regions, due to increased international travel and globalization. Carbapenems are earmarked as potentially active drugs for the treatment of To better understand the potential of carbapenems for the treatment of M/XDR-TB, the aim of this review was to evaluate the literature on currently available , , and clinical data on carbapenems in the treatment of and to detect knowledge gaps, in order to target future research. In February 2018, a systematic literature search of PubMed and Web of Science was performed. Overall, the results of the studies identified in this review, which used a variety of carbapenem susceptibility tests on clinical and laboratory strains of , are consistent. , the activity of carbapenems against is increased when used in combination with clavulanate, a BLaC inhibitor. However, clavulanate is not commercially available alone, and therefore, it is impossible in practice to prescribe carbapenems in combination with clavulanate at this time. Few studies have been performed, including one prospective, two observational, and seven retrospective clinical studies to assess the effectiveness, safety, and tolerability of three different carbapenems (imipenem, meropenem, and ertapenem). We found no clear evidence at the present time to select one particular carbapenem among the different candidate compounds to design an effective M/XDR-TB regimen. Therefore, more clinical evidence and dose optimization substantiated by hollow-fiber infection studies are needed to support repurposing carbapenems for the treatment of M/XDR-TB.
耐多药和广泛耐药结核病(M/XDR-TB)不仅在结核病负担高的国家,而且在富裕地区也构成了日益严重的威胁,这是由于国际旅行和全球化的增加所致。碳青霉烯类抗生素被指定为治疗耐多药和广泛耐药结核病的潜在有效药物。为了更好地了解碳青霉烯类抗生素治疗 M/XDR-TB 的潜力,本综述旨在评估目前可用于治疗耐多药和广泛耐药结核病的碳青霉烯类抗生素的文献,以及关于碳青霉烯类抗生素治疗耐多药和广泛耐药结核病的临床数据,并发现知识空白,以便针对未来的研究。2018 年 2 月,对 PubMed 和 Web of Science 进行了系统的文献检索。总的来说,本综述中确定的研究结果一致,这些研究使用了各种碳青霉烯类抗生素敏感性试验,对耐多药和广泛耐药结核分枝杆菌的临床和实验室菌株进行了评估。结果表明,当碳青霉烯类抗生素与克拉维酸(一种 BLaC 抑制剂)联合使用时,其对耐多药和广泛耐药结核分枝杆菌的活性增加。然而,克拉维酸目前并未单独上市,因此实际上不可能在此时开处方联合使用碳青霉烯类抗生素和克拉维酸。仅有少数耐多药和广泛耐药结核病的研究,包括一项前瞻性研究、两项观察性研究和七项回顾性临床研究,评估了三种不同碳青霉烯类抗生素(亚胺培南、美罗培南和厄他培南)的有效性、安全性和耐受性。目前,我们没有明确的证据可以在不同候选化合物中选择一种特定的碳青霉烯类抗生素来设计有效的耐多药和广泛耐药结核病方案。因此,需要更多的临床证据和空心纤维感染研究来支持碳青霉烯类抗生素在耐多药和广泛耐药结核病治疗中的重新定位。