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Updated: Jun 3, 2026

Design of Cecal Ligation and Puncture and Intranasal Infection Dual Model of Sepsis-Induced Immunosuppression
Published on: June 15, 2019
[Collateral damage and hospital infections]
Miodrag Vrbić1, Biljana Vrbić, Radmila Velicković-Radovanovanović
1Klinika za zarazne bolesti, Klinicki centar Nis, Nis. mvrbic@eunet.rs
Abstract:
COLLATERAL DAMAGE: Implies negative ecological effects of antibiotic therapy, characterized by the selection of resistant microorganisms and adverse colonization or injections with their multi-resistant species. MICROBIAL RESISTANCE: Is mediated by various mechanisms, the presence of which is determined by the nature of antibiotic effects and origin of the agent. Its most important aspect is multiple resistance, most commonly conditioned by the presence of several different resistance genes localized in the form of common units on gene transport elements (integrons, transposons, plasmids). It is further developed by way of mutation-guided alterations in the environments with a strong, selective antibiotic pressure, such as hospital conditions. HOSPITAL INFECTIONS: Bacteremias and pneumonias, above all, are nowadays the principal cause of hospital morbidity and mortality. More than 70% of agents causing them are resistant to at least one of the antibiotics to which they were sensitive once, and multi-resistance is their very common feature as well. Currently valid recommendations for the treatment of nosocomial bacteremias and pneumonias are the empirical application of broad spectrum antibiotics, de-escalation treatment, short therapy course. use of bactericidal antibiotics, and optimization of their pharmacodynamics. in that regard, a combined treatment with carbapenems and glycopeptides reduces the probability of inadequate onset of treatment and the risk of further development of microbial resistance (in some cases it also mediates the establishment of earlier sensitivity), it shortens treatment time, and reduces treatment costs. Further improvement of such a treatment involves a possible adjustment to the well known and regularly monitored local incidence and resistance of microbial agents.
Insights
Antibiotic therapy can lead to collateral damage by promoting microbial resistance. Combined treatments with carbapenems and glycopeptides offer a strategy to combat hospital infections and reduce resistance development.
Area of Science:
- Microbiology
- Pharmacology
- Infectious Diseases
Context:
- Antibiotic therapy exerts ecological pressure, selecting for resistant microorganisms.
- Hospital-acquired infections, particularly bacteremias and pneumonias, are significant causes of morbidity and mortality.
- A high prevalence of multi-drug resistant pathogens complicates the treatment of nosocomial infections.
Purpose:
- To explore the mechanisms and consequences of antibiotic-induced microbial resistance.
- To evaluate current treatment strategies for hospital-acquired infections.
- To assess the efficacy of combined antibiotic therapies in managing resistant pathogens.
Summary:
- Collateral damage from antibiotics includes the selection and proliferation of multi-resistant microorganisms.
- Microbial resistance is driven by gene transfer elements like integrons and transposons, exacerbated by hospital environments.
- Combined therapy with carbapenems and glycopeptides shows promise in reducing treatment failures and resistance.
- Treatment optimization involves tailoring empirical broad-spectrum antibiotic use to local resistance patterns.
Impact:
- Reduced incidence of inadequate treatment onset for nosocomial infections.
- Decreased risk of further microbial resistance development.
- Shorter treatment durations and lower healthcare costs associated with hospital-acquired infections.
- Improved patient outcomes through optimized antimicrobial pharmacodynamics and de-escalation strategies.
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