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氨曲南与阿维巴坦联合用于治疗产金属β-内酰胺酶革兰阴性菌的研究进展:体外研究与临床病例的系统评价

The Revival of Aztreonam in Combination with Avibactam against Metallo-β-Lactamase-Producing Gram-Negatives: A Systematic Review of In Vitro Studies and Clinical Cases.

作者信息

Mauri Carola, Maraolo Alberto Enrico, Di Bella Stefano, Luzzaro Francesco, Principe Luigi

机构信息

Clinical Microbiology and Virology Unit, "A. Manzoni" Hospital, 23900 Lecco, Italy.

First Division of Infectious Diseases, Cotugno Hospital, AORN dei Colli, 80131 Naples, Italy.

出版信息

Antibiotics (Basel). 2021 Aug 20;10(8):1012. doi: 10.3390/antibiotics10081012.

DOI:10.3390/antibiotics10081012
PMID:34439062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8388901/
Abstract

Infections caused by metallo-β-lactamase (MBL)-producing and are increasingly reported worldwide and are usually associated with high mortality rates (>30%). Neither standard therapy nor consensus for the management of these infections exist. Aztreonam, an old β-lactam antibiotic, is not hydrolyzed by MBLs. However, since many MBL-producing strains co-produce enzymes that could hydrolyze aztreonam (e.g., AmpC, ESBL), a robust β-lactamase inhibitor such as avibactam could be given as a partner drug. We performed a systematic review including 35 in vitro and 18 in vivo studies on the combination aztreonam + avibactam for infections sustained by MBL-producing Gram-negatives. In vitro data on 2209 Gram-negatives were available, showing the high antimicrobial activity of aztreonam (MIC ≤ 4 mg/L when combined with avibactam) in 80% of MBL-producing , 85% of and 6% of MBL-producing . Clinical data were available for 94 patients: 83% of them had bloodstream infections. Clinical resolution within 30 days was reported in 80% of infected patients. Analyzing only patients with bloodstream infections (64 patients), death occurred in 19% of patients treated with aztreonam + ceftazidime/avibactam. The combination aztreonam + avibactam appears to be a promising option against MBL-producing bacteria (especially , much less for ) while waiting for new antimicrobials.

摘要

由产金属β-内酰胺酶(MBL)的细菌引起的感染在全球范围内的报道日益增多,且通常与高死亡率(>30%)相关。目前对于这些感染既没有标准治疗方法,也没有管理共识。氨曲南是一种老一代的β-内酰胺抗生素,不会被MBL水解。然而,由于许多产MBL的菌株还会共同产生能水解氨曲南的酶(如AmpC、超广谱β-内酰胺酶),因此可以给予一种强效的β-内酰胺酶抑制剂如阿维巴坦作为联合用药。我们进行了一项系统评价,纳入了35项关于氨曲南+阿维巴坦联合用于产MBL革兰阴性菌所致感染的体外研究和18项体内研究。有2209株革兰阴性菌的体外数据,结果显示氨曲南(与阿维巴坦联合时MIC≤4mg/L)对80%的产MBL大肠埃希菌、85%的肺炎克雷伯菌和6%的产MBL铜绿假单胞菌具有高抗菌活性。有94例患者的临床数据:其中83%患有血流感染。80%的感染患者在30天内临床症状缓解。仅分析血流感染患者(64例),接受氨曲南+头孢他啶/阿维巴坦治疗的患者中有19%死亡。在等待新型抗菌药物出现期间,氨曲南+阿维巴坦联合用药似乎是对抗产MBL细菌(尤其是大肠埃希菌,对铜绿假单胞菌效果差得多)的一个有前景的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/cdae25c21440/antibiotics-10-01012-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/ebceaebc359e/antibiotics-10-01012-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/cd90ad5382ca/antibiotics-10-01012-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/cdae25c21440/antibiotics-10-01012-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/ebceaebc359e/antibiotics-10-01012-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/cd90ad5382ca/antibiotics-10-01012-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8388901/cdae25c21440/antibiotics-10-01012-g003.jpg

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