Therapeutic options for difficult-to-treat A
Acinetobacter Infections
/ drug therapy
Acinetobacter baumannii
/ drug effects
Anti-Bacterial Agents
/ therapeutic use
Drug Resistance, Multiple, Bacterial
Fluoroquinolones
/ therapeutic use
Humans
Microbial Sensitivity Tests
Randomized Controlled Trials as Topic
beta-Lactamase Inhibitors
/ therapeutic use
beta-Lactams
/ therapeutic use
Acinetobacter
MDR
XDR
cefiderocol
durlobactam/sulbactam
eravacycline
Journal
Expert opinion on pharmacotherapy
ISSN: 1744-7666
Titre abrégé: Expert Opin Pharmacother
Pays: England
ID NLM: 100897346
Informations de publication
Date de publication:
Feb 2021
Feb 2021
Historique:
pubmed:
12
9
2020
medline:
24
2
2021
entrez:
11
9
2020
Statut:
ppublish
Résumé
Treatment of severe infections due to The present perspective provides a personal view on both current and future agents for the treatment of severe DTR-AB infections. We currently are in a transition era for the treatment of DTR-AB infections, where in the past 20 years, polymyxin-based regimens have become the most used approach (although possibly suboptimal, there were few or no alternatives) and where in the next 20 years, polymyxins will likely be replaced by less toxic novel agents as first-line choices. Two novel antimicrobial agents have been recently approved that show activity against DTR-AB, cefiderocol and eravacycline, while durlobactam/sulbactam is in phase-3 of clinical development. In the near future, these agents could become important first-line choices for the treatment of DTR-AB within approved indications, or for off-label indications in the absence of dependable alternatives. Good-quality post-marketing experiences remain necessary for arising clinically relevant questions and guiding the design of further dedicated randomized controlled trials to stably optimize the use of novel agents for DTR-AB infections in the next decades.
Identifiants
pubmed: 32915685
doi: 10.1080/14656566.2020.1817386
doi:
Substances chimiques
Anti-Bacterial Agents
0
Fluoroquinolones
0
beta-Lactamase Inhibitors
0
beta-Lactams
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM