[New β‑lactam antibiotics and β‑lactamase inhibitors against multidrug-resistant Gram-negative bacteria]

Alexander Mischnik1, Christoph Lübbert2, Nico T Mutters3

  • 1Klinik für Infektiologie und Mikrobiologie, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee 160, 23562, Lübeck, Deutschland. alexander.mischnik@uksh.de.

Der Internist
|September 29, 2018
PubMed
Abstract

Insights

New antibiotics offer options against multidrug-resistant Gram-negative bacteria (MDR-GN), but challenges remain for metallo-β-lactamase (MBL) producers. Further research is needed on efficacy, toxicity, and dosing for these critical infections.

Area of Science:

  • Infectious Diseases
  • Pharmacology
  • Microbiology

Background:

  • The global rise of multidrug-resistant Gram-negative bacteria (MDR-GN) presents a significant public health challenge.
  • Limited treatment options are available for MDR-GN infections, with few new drugs in late-stage development or approved.

Purpose of the Study:

  • To review current data on novel beta-lactam antibiotics and beta-lactamase inhibitor combinations for treating MDR-GN infections.
  • This review excludes new macrolides, ketolides, and aminoglycosides.

Main Methods:

  • A selective literature search was conducted on published data and registered trials.
  • Key agents reviewed include ceftazidime/avibactam, ceftolozane/tazobactam, imipenem/cilastatin + relebactam, meropenem/vaborbactam, aztreonam/avibactam, and cefiderocol.

Main Results:

  • New antimicrobial agents provide additional treatment choices for MDR-GN infections.
  • These agents demonstrate efficacy against beta-lactamase-producing bacteria, but effectiveness varies.
  • Currently, no adequate treatment options exist for infections caused by metallo-beta-lactamase (MBL) producers.

Conclusions:

  • Clinical data are limited and derived from heterogeneous patient groups, making direct comparisons difficult.
  • Early resistance development has been observed.
  • The optimal use, including toxicity and dosing in organ dysfunction or failure, requires further clarification.

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