Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>

Antimicrobial combinations are at the moment the only potential treatment option for pandrug-resistant <i>A. baumannii</i>. A systematic review was conducted in PubMed and Scopus for studies reporting the activity of antimicrobial combinations against <i>A. baumannii</i> resi...

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Autores principales: Stamatis Karakonstantis, Petros Ioannou, George Samonis, Diamantis P. Kofteridis
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:4ecb6916b7fd4a9d9b648d1d5bdb55512021-11-25T16:23:14ZSystematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>10.3390/antibiotics101113442079-6382https://doaj.org/article/4ecb6916b7fd4a9d9b648d1d5bdb55512021-11-01T00:00:00Zhttps://www.mdpi.com/2079-6382/10/11/1344https://doaj.org/toc/2079-6382Antimicrobial combinations are at the moment the only potential treatment option for pandrug-resistant <i>A. baumannii</i>. A systematic review was conducted in PubMed and Scopus for studies reporting the activity of antimicrobial combinations against <i>A. baumannii</i> resistant to all components of the combination. The clinical relevance of synergistic combinations was assessed based on concentrations achieving synergy and PK/PD models. Eighty-four studies were retrieved including 818 eligible isolates. A variety of combinations (<i>n</i> = 141 double, <i>n</i> = 9 triple) were tested, with a variety of methods. Polymyxin-based combinations were the most studied, either as double or triple combinations with cell-wall acting agents (including sulbactam, carbapenems, glycopeptides), rifamycins and fosfomycin. Non-polymyxin combinations were predominantly based on rifampicin, fosfomycin, sulbactam and avibactam. Several combinations were synergistic at clinically relevant concentrations, while triple combinations appeared more active than the double ones. However, no combination was consistently synergistic against all strains tested. Notably, several studies reported synergy but at concentrations unlikely to be clinically relevant, or the concentration that synergy was observed was unclear. Selecting the most appropriate combinations is likely strain-specific and should be guided by in vitro synergy evaluation. Furthermore, there is an urgent need for clinical studies on the efficacy and safety of such combinations.Stamatis KarakonstantisPetros IoannouGeorge SamonisDiamantis P. KofteridisMDPI AGarticle<i>Acinetobacter</i>pandrug-resistantantimicrobial combinationssynergyTherapeutics. PharmacologyRM1-950ENAntibiotics, Vol 10, Iss 1344, p 1344 (2021)
institution DOAJ
collection DOAJ
language EN
topic <i>Acinetobacter</i>
pandrug-resistant
antimicrobial combinations
synergy
Therapeutics. Pharmacology
RM1-950
spellingShingle <i>Acinetobacter</i>
pandrug-resistant
antimicrobial combinations
synergy
Therapeutics. Pharmacology
RM1-950
Stamatis Karakonstantis
Petros Ioannou
George Samonis
Diamantis P. Kofteridis
Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>
description Antimicrobial combinations are at the moment the only potential treatment option for pandrug-resistant <i>A. baumannii</i>. A systematic review was conducted in PubMed and Scopus for studies reporting the activity of antimicrobial combinations against <i>A. baumannii</i> resistant to all components of the combination. The clinical relevance of synergistic combinations was assessed based on concentrations achieving synergy and PK/PD models. Eighty-four studies were retrieved including 818 eligible isolates. A variety of combinations (<i>n</i> = 141 double, <i>n</i> = 9 triple) were tested, with a variety of methods. Polymyxin-based combinations were the most studied, either as double or triple combinations with cell-wall acting agents (including sulbactam, carbapenems, glycopeptides), rifamycins and fosfomycin. Non-polymyxin combinations were predominantly based on rifampicin, fosfomycin, sulbactam and avibactam. Several combinations were synergistic at clinically relevant concentrations, while triple combinations appeared more active than the double ones. However, no combination was consistently synergistic against all strains tested. Notably, several studies reported synergy but at concentrations unlikely to be clinically relevant, or the concentration that synergy was observed was unclear. Selecting the most appropriate combinations is likely strain-specific and should be guided by in vitro synergy evaluation. Furthermore, there is an urgent need for clinical studies on the efficacy and safety of such combinations.
format article
author Stamatis Karakonstantis
Petros Ioannou
George Samonis
Diamantis P. Kofteridis
author_facet Stamatis Karakonstantis
Petros Ioannou
George Samonis
Diamantis P. Kofteridis
author_sort Stamatis Karakonstantis
title Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>
title_short Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>
title_full Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>
title_fullStr Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>
title_full_unstemmed Systematic Review of Antimicrobial Combination Options for Pandrug-Resistant <i>Acinetobacter baumannii</i>
title_sort systematic review of antimicrobial combination options for pandrug-resistant <i>acinetobacter baumannii</i>
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/4ecb6916b7fd4a9d9b648d1d5bdb5551
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