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Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Late onset ventilator-associated pneumonia due to multidrug-resistant Acinetobacter spp.: experience with tigecycline
D Curcio1, F Fernández, J Vergara
1Infectología Institucional SRL, Buenos Aires, Argentina. djcurcio@gmail.com
Abstract:
The aim of the study was to evaluate the clinical success rate of 73 patients with ventilator-associated pneumonia (VAP) caused by multidrug-resistant (MDR)-Acinetobacter spp. treated with tigecycline in seven intensive Care Units in Argentina and to determine which predictor variables were significant in this context. Clinical success in our patients was 69.86% (Ci= 58.65-81.07%) 51/73, without significant differences between patients with VAP due to MDR-Acinetobacter spp. carbapenem-susceptible or carbapenem-resistant and only susceptible to colistin, minocyline and tigecycline (70% 44/73 vs. 69% 29/73 respectively, p=0.9006), and between patients who received <48h of prior antibiotics (including those who did not receive any) and those who received >48h of prior antibiotics (73.3% 22/30 vs 67.4% 29/43 respectively, p=0.7791). Age >67 and using other method than BAL for respiratory sampling were identified as predicting variables for negative clinical outcome. Our results suggest that tigecycline may be an acceptable alternative for therapy in patients with VAP caused by MDR-Acinetobacter spp. Nevertheless, only controlled clinical trials will provide the evidence to support approval for new indications.
Insights
Tigecycline shows a 69.86% clinical success rate for treating ventilator-associated pneumonia (VAP) caused by multidrug-resistant Acinetobacter spp. Older age and non-bronchoalveolar lavage sampling predict negative outcomes.
Area of Science:
- Infectious Diseases
- Critical Care Medicine
- Antimicrobial Stewardship
Background:
- Ventilator-associated pneumonia (VAP) poses a significant challenge, particularly when caused by multidrug-resistant (MDR) Acinetobacter spp.
- Limited treatment options exist for VAP due to MDR Acinetobacter infections, necessitating evaluation of alternative therapies.
Purpose of the Study:
- To assess the clinical success rate of tigecycline in treating VAP caused by MDR Acinetobacter spp.
- To identify predictor variables associated with clinical outcomes in this patient population.
Main Methods:
- A retrospective study evaluating 73 patients with VAP due to MDR Acinetobacter spp. treated with tigecycline across seven intensive care units.
- Analysis of clinical success rates and identification of significant predictor variables for treatment outcomes.
Main Results:
- Overall clinical success rate with tigecycline was 69.86% (51/73 patients).
- No significant differences in success rates were observed based on carbapenem resistance or prior antibiotic duration.
- Age over 67 and non-bronchoalveolar lavage (BAL) respiratory sampling were identified as predictors of negative clinical outcomes.
Conclusions:
- Tigecycline appears to be a viable therapeutic option for VAP caused by MDR Acinetobacter spp.
- Further evidence from controlled clinical trials is needed to support tigecycline's approval for new indications in VAP treatment.
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