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Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Therapeutics for Vancomycin-Resistant Enterococcal Bloodstream Infections
Kelly A Cairns1,2, Andrew A Udy3,4, Trisha N Peel1
1Department of Infectious Diseases, The Alfred Hospital and Central Clinical School, Monash University, Melbourne, Victoria, Australia.
Abstract:
Vancomycin-resistant enterococci (VRE) are common causes of bloodstream infections (BSIs) with high morbidity and mortality rates. They are pathogens of global concern with a limited treatment pipeline. Significant challenges exist in the management of VRE BSI, including drug dosing, the emergence of resistance, and the optimal treatment for persistent bacteremia and infective endocarditis. Therapeutic drug monitoring (TDM) for antimicrobial therapy is evolving for VRE-active agents; however, there are significant gaps in the literature for predicting antimicrobial efficacy for VRE BSIs. To date, TDM has the greatest evidence for predicting drug toxicity for the three main VRE-active antimicrobial agents daptomycin, linezolid, and teicoplanin. This article presents an overview of the treatment options for VRE BSIs, the role of antimicrobial dose optimization through TDM in supporting clinical infection management, and challenges and perspectives for the future.
Insights
Vancomycin-resistant enterococci (VRE) bloodstream infections pose significant treatment challenges. Optimizing antimicrobial dosing through therapeutic drug monitoring (TDM) is crucial for managing VRE infections and improving patient outcomes.
Area of Science:
- Infectious Diseases
- Clinical Pharmacology
- Microbiology
Background:
- Vancomycin-resistant enterococci (VRE) are a major cause of hospital-acquired bloodstream infections (BSIs), associated with high morbidity and mortality.
- Limited treatment options and emerging resistance complicate VRE BSI management, necessitating strategies for antimicrobial dose optimization.
- Challenges include drug dosing, resistance, persistent bacteremia, and infective endocarditis treatment.
Purpose of the Study:
- To provide an overview of current treatment strategies for VRE BSIs.
- To discuss the role of therapeutic drug monitoring (TDM) in optimizing antimicrobial therapy for VRE infections.
- To highlight challenges and future perspectives in managing VRE BSIs.
Main Methods:
- Review of existing literature on VRE BSI treatment and therapeutic drug monitoring (TDM).
- Analysis of evidence for TDM in predicting drug toxicity and efficacy of VRE-active agents.
- Discussion of clinical management challenges and future research directions.
Main Results:
- Therapeutic drug monitoring (TDM) shows the most evidence for predicting drug toxicity with daptomycin, linezolid, and teicoplanin.
- Significant gaps exist in predicting antimicrobial efficacy for VRE BSIs using TDM.
- Optimizing antimicrobial dosing through TDM is a key area for supporting clinical infection management.
Conclusions:
- Effective management of VRE BSIs requires careful consideration of treatment options and antimicrobial dosing.
- Therapeutic drug monitoring (TDM) plays a vital role in optimizing antimicrobial therapy, particularly for toxicity prediction.
- Further research is needed to address gaps in predicting antimicrobial efficacy for VRE BSIs through TDM.
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