Literature DB >> 28162982

Revival of old antibiotics: needs, the state of evidence and expectations.

Hiba Zayyad1, Noa Eliakim-Raz2, Leonard Leibovici2, Mical Paul3.   

Abstract

The gap between the emergence of antibiotic resistance and new antibiotic development has drawn attention to old antibiotics whose spectrum of coverage frequently comprises highly resistant bacteria. However, these antibiotics have frequently not undergone the structured process of antibiotic development of modern antibiotics, from pharmacokinetic/pharmacodynamic (PK/PD) studies establishing safe and effective dosing, establishment of susceptibility breakpoints, to clinical trials establishing clinical safety and effectiveness. In this review, we highlight the gaps for which we need old antibiotics in community- and hospital-acquired infections. Reviewing recently published and ongoing randomised controlled trials (RCTs) shows advances in our understanding of the efficacy and effectiveness of oral fosfomycin, mecillinam and nitrofurantoin for cystitis, and of trimethoprim/sulfamethoxazole for complicated skin infections caused by methicillin-resistant Staphylococcus aureus (MRSA) in the community. Summarising older evidence shows the inferiority of chloramphenicol versus modern antibiotics for severe infections. We lack studies on severe infections caused by carbapenem-resistant Gram-negative bacteria and other multidrug-resistant (MDR) bacteria in hospitalised and critically ill patients; ongoing studies assessing colistin and intravenous fosfomycin might fill in some gaps. In the re-development process of old antibiotics, we mandate modern PK/PD studies comprising special populations as well as RCTs addressing the target population of patients in need of these antibiotics powered to examine patient-relevant outcomes. Structured antibiotic re-development from the laboratory to evidence-based treatment recommendations requires public funding, multidisciplinary collaboration, international co-ordination, and methods to streamline the recruitment of critically ill patients infected by MDR bacteria.
Copyright © 2017 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.

Entities:  

Keywords:  Carbapenem-resistant Enterobacteriaceae; Carbapenem-resistant Gram-negative bacteria; Evidence-based medicine; MRSA; Polymyxins

Mesh:

Substances:

Year:  2017        PMID: 28162982     DOI: 10.1016/j.ijantimicag.2016.11.021

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  9 in total

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2.  Tet38 Efflux Pump Contributes to Fosfomycin Resistance in Staphylococcus aureus.

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Authors:  S M S Ng; J S P Sioson; J M Yap; F M Ng; H S V Ching; J W P Teo; R Jureen; J Hill; C S B Chia
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2017-10-10       Impact factor: 3.267

4.  The Role of fosA in Challenges with Fosfomycin Susceptibility Testing of Multispecies Klebsiella pneumoniae Carbapenemase-Producing Clinical Isolates.

Authors:  Zachary S Elliott; Katie E Barry; Heather L Cox; Nicole Stoesser; Joanne Carroll; Kasi Vegesana; Shireen Kotay; Anna E Sheppard; Alex Wailan; Derrick W Crook; Hardik Parikh; Amy J Mathers
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5.  Unraveling Mechanisms and Epidemic Characteristics of Nitrofurantoin Resistance in Uropathogenic Enterococcus faecium Clinical Isolates.

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6.  Bactericidal Activity of Sodium Bituminosulfonate against Staphylococcus aureus.

Authors:  Elisa Heuser; Karsten Becker; Evgeny A Idelevich
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7.  Activity of fosfomycin against nosocomial multiresistant bacterial pathogens from Croatia: a multicentric study.

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Journal:  Croat Med J       Date:  2018-04-30       Impact factor: 1.351

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Authors:  Mikaeel Young; Ali Ozcan; Briana Lee; Tyler Maxwell; Thomas Andl; Parthiban Rajasekaran; Melanie J Beazley; Laurene Tetard; Swadeshmukul Santra
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Review 9.  Treatment options for K. pneumoniae, P. aeruginosa and A. baumannii co-resistant to carbapenems, aminoglycosides, polymyxins and tigecycline: an approach based on the mechanisms of resistance to carbapenems.

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Journal:  Infection       Date:  2020-09-01       Impact factor: 3.553

  9 in total

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