First case report of a vertebral osteomyelitis caused by carbapenem-resistant Enterobacter cloacae treated with imipenem/cilastatin/relebactam prolonged infusion then meropenem/vaborbactam in continuous infusion.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2024-10-30 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1347306
Paul Laffont-Lozes, Tayma Naciri, Alix Pantel, Aurélie Martin, Anne-Sophie Pruvot-Occean, Vincent Haignere, Paul Loubet, Albert Sotto, Romaric Larcher
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引用次数: 0

Abstract

Introduction: Bone and joint infections (BJIs) caused by multidrug-resistant bacteria are becoming more frequent. However, data on the use of novel β-lactam/β-lactamase inhibitors, such as imipenem/cilastatin/relebactam (I-R) and meropenem/vaborbactam (MVB), to treat BJIs is lacking. Furthermore, prolonged infusions of these β-lactams should theoretically optimize pharmacokinetic/pharmacodynamics target in these indications, but there are currently no reports on this type of infusions, especially in the setting of BJI.

Case presentation: We report a case of a vertebral osteomyelitis caused by carbapenem-resistant Enterobacter cloacae successfully treated with extended-infusion of I-R (1.25 g q6h over 2 h), then with continuous infusion of MVB (2 g q4h as over 4 h). Therapeutic drug monitoring confirmed that extended-infusion of I-R and continuous infusion of MVB achieved serum concentrations up to 12 mg/L of imipenem and 19 mg/L of meropenem, respectively.

Conclusion: The favourable outcome of this patient treated for a vertebral osteomyelitis caused by carbapenem-resistant E. cloacae suggest that extended- and continuous infusions of I-R and MVB, are promising regimens for treatment of BJIs caused by carbapenem-resistant Enterobacterales.

首例耐碳青霉烯类肠杆菌引起的脊椎骨髓炎病例报告,患者先接受亚胺培南/西司他丁/雷巴坦长期输注治疗,然后接受美罗培南/伐硼巴坦持续输注治疗。
导言:耐多药细菌引起的骨与关节感染(BJI)越来越频繁。然而,目前还缺乏使用新型β-内酰胺/β-内酰胺酶抑制剂(如亚胺培南/西司他丁/雷巴坦(I-R)和美罗培南/伐硼内酰胺(MVB))治疗骨关节感染的数据。此外,在这些适应症中,长时间输注这些β-内酰胺类药物理论上应可优化药代动力学/药效学目标,但目前还没有关于这种输注方式的报道,尤其是在 BJI 的情况下:我们报告了一例由耐碳青霉烯类肠杆菌引起的椎体骨髓炎病例,患者先接受了 I-R 延长输注(1.25 克,q6h,持续 2 小时),然后又接受了 MVB 持续输注(2 克,q4h,持续 4 小时)。治疗药物监测证实,延长输注 I-R 和持续输注 MVB 可使亚胺培南和美罗培南的血清浓度分别达到 12 毫克/升和 19 毫克/升:结论:这名由耐碳青霉烯类肠杆菌引起的脊椎骨髓炎患者的良好疗效表明,延长输注 I-R 和持续输注 MVB 是治疗由耐碳青霉烯类肠杆菌引起的 BJI 的有效方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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