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Updated: Apr 7, 2026

Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Unveiling Antibiotic Resistance in Ventilator-Associated Pneumonia Patients: A Comprehensive Analysis
Arti Agrawal1, Pragya Shakya1, Parul Garg1
1Microbiology, Sarojini Naidu Medical College, Agra, IND.
Ventilator-associated pneumonia (VAP) is common in ICUs, driven by multidrug-resistant Gram-negative bacteria like Acinetobacter baumannii. Early culture-guided treatment is vital to combat resistance and improve patient outcomes.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Microbiology
Background:
- Ventilator-associated pneumonia (VAP) is a significant healthcare-associated infection, particularly in resource-limited settings with prevalent multidrug-resistant organisms.
- Assessing the bacteriological profile and antimicrobial susceptibility of endotracheal aspirates is crucial for VAP management.
Purpose of the Study:
- To determine the bacteriological profile and antimicrobial susceptibility patterns of endotracheal aspirates in VAP patients.
- To compare microbial distribution between early-onset and late-onset VAP.
Main Methods:
- A descriptive cross-sectional study included adult patients mechanically ventilated for over 48 hours with suspected VAP (CPIS score >6).
- Endotracheal aspirates were cultured semi-quantitatively (≥10⁵ CFU/mL significant), and antimicrobial susceptibility testing was performed.
- Demographic data, risk factors, isolates, and resistance patterns were analyzed using chi-square tests.
Main Results:
- VAP incidence was 32.7% (195/596 patients), with an incidence density of 33.6 per 1000 ventilator-days.
- Gram-negative pathogens predominated (76.1% early vs. 78% late VAP), with Acinetobacter baumannii being the most common isolate.
- Extensive multidrug resistance was observed; only polymyxin B and colistin showed universal susceptibility. Carbapenem susceptibility varied, with higher sensitivity in late-onset A. baumannii.
Conclusions:
- The high burden of VAP is driven by multidrug-resistant Gram-negative organisms, especially Acinetobacter baumannii and Klebsiella pneumoniae.
- Strengthened antimicrobial stewardship, resistance surveillance, and VAP prevention bundles are urgently needed.
- Early culture-guided de-escalation is essential for optimizing patient outcomes and controlling antimicrobial resistance.
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