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Updated: Aug 9, 2025

Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Ventilator-Associated Pneumonia in Immunosuppressed Patients
Louis Kreitmann1,2,3, Alexandre Gaudet1,4, Saad Nseir1,5
1Médecine Intensive Réanimation, CHU de Lille, F-59000 Lille, France.
Ventilator-associated lower respiratory tract infections (VA-LTRI), including pneumonia (VAP) and tracheobronchitis (VAT), may occur less frequently in immunocompromised patients. This review examines VAP/VAT features, diagnosis, and outcomes in this vulnerable population.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Immunology
Background:
- Immunocompromised patients represent a growing segment of critically-ill individuals, facing heightened risks of healthcare-associated infections.
- Ventilator-associated lower respiratory tract infections (VA-LTRI), encompassing ventilator-associated pneumonia (VAP) and tracheobronchitis (VAT), are common in intensive care units (ICUs).
Purpose of the Study:
- To review the specific characteristics of VAP and VAT in immunocompromised patients.
- To discuss recent findings challenging previous beliefs on VAP/VAT incidence and multidrug-resistant (MDR) bacteria in this population.
Main Methods:
- Narrative review of recent literature on VAP and VAT in immunocompromised patients.
- Discussion of diagnostic approaches, including invasive sampling (e.g., bronchoscopy with bronchoalveolar lavage) and molecular tools.
- Examination of epidemiological data, pathogen prevalence (including opportunistic pathogens), and treatment strategies.
Main Results:
- Contrary to prior assumptions, VAP and VAT incidence may be lower in immunocompromised patients compared to non-immunocompromised individuals.
- The association between immunosuppression and MDR bacterial VAP/VAT has been recently questioned.
- Gram-negative bacteria are common, but opportunistic pathogens require specific diagnostic consideration in immunocompromised hosts.
Conclusions:
- Immunocompromised status may not increase VAP/VAT incidence, and the role of MDR bacteria needs re-evaluation.
- Accurate etiological diagnosis is crucial for effective treatment selection in these patients.
- Further research is needed to understand the impact of immunosuppression on VAP/VAT outcomes and optimize empirical antibiotic regimens.
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