Novel Antibiotics for Gram-Negative Nosocomial Pneumonia

Author:

Almyroudi Maria Panagiota1ORCID,Chang Aina23,Andrianopoulos Ioannis4ORCID,Papathanakos Georgios4ORCID,Mehta Reena256ORCID,Paramythiotou Elizabeth7ORCID,Koulenti Despoina28

Affiliation:

1. Emergency Department, Attikon University Hospital, National and Kapodistrian University of Athens, 12462 Athens, Greece

2. Department of Critical Care Medicine, King’s College Hospital NHS Foundation Trust, London SE5 9RS, UK

3. Department of Haematology, King’s College London, London SE5 9RS, UK

4. Department of Critical Care, University Hospital of Ioannina, University of Ioannina, 45110 Ioannina, Greece

5. Pharmacy Department, King’s College Hospital NHS Foundation Trust, London SE5 9RS, UK

6. School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, Kings College London, London SE5 9RS, UK

7. Department of Critical Care, Laikon Hospital, 11527 Athens, Greece

8. Antibiotic Optimisation Group, UQ Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane 4029, Australia

Abstract

Nosocomial pneumonia, including hospital-acquired pneumonia and ventilator-associated pneumonia, is the leading cause of death related to hospital-acquired infections among critically ill patients. A growing proportion of these cases are attributed to multi-drug-resistant (MDR-) Gram-negative bacteria (GNB). MDR-GNB pneumonia often leads to delayed appropriate treatment, prolonged hospital stays, and increased morbidity and mortality. This issue is compounded by the increased toxicity profiles of the conventional antibiotics required to treat MDR-GNB infections. In recent years, several novel antibiotics have been licensed for the treatment of GNB nosocomial pneumonia. These novel antibiotics are promising therapeutic options for treatment of nosocomial pneumonia by MDR pathogens with certain mechanisms of resistance. Still, antibiotic resistance remains an evolving global crisis, and resistance to novel antibiotics has started emerging, making their judicious use crucial to prolong their shelf-life. This article presents an up-to-date review of these novel antibiotics and their current role in the antimicrobial armamentarium. We critically present data for the pharmacokinetics/pharmacodynamics, the in vitro spectrum of antimicrobial activity and resistance, and in vivo data for their clinical and microbiological efficacy in trials. Where possible, available data are summarized specifically in patients with nosocomial pneumonia, as this cohort may exhibit ‘critical illness’ physiology that affects drug efficacy.

Publisher

MDPI AG

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