4.7 Article

Ventilator-Associated Tracheobronchitis and Pneumonia: Thinking Outside the Box

Journal

CLINICAL INFECTIOUS DISEASES
Volume 51, Issue -, Pages S59-S66

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1086/653051

Keywords

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Funding

  1. Bard
  2. Pfizer
  3. Merck
  4. Covidien
  5. Wyeth
  6. Sanofi Pasteur
  7. Ortho McNeil
  8. Bard Pharmaceuticals
  9. US Food and Drug Administration
  10. Infectious Diseases Society of America
  11. American College of Chest Physicians
  12. American Thoracic Society
  13. Society of Critical Care Medicine
  14. Pharmaceutical Research and Manufacturers of America
  15. AstraZeneca Pharmaceuticals
  16. Forest Pharmaceuticals

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Lower respiratory tract infections in intubated patients include ventilator-associated tracheobronchitis (VAT) and ventilator-associated pneumonia (VAP). These infections are increasingly caused by multidrug-resistant bacteria, which colonize the patient's oropharynx and enter the lower respiratory tract around the endotracheal tube cuff or through the lumen. Progression of colonization to VAT and, in some patients, to VAP is related to the quantity, types, and virulence of invading bacteria versus containment by host defenses. Diagnostic criteria for VAT and VAP overlap in terms of clinical signs and symptoms, and they share similar microbiologic criteria when endotracheal sputum aspirate samples are used. In addition, the diagnosis of VAP requires a new and persistent infiltrate on a chest radiograph, which may be difficult to assess in critically ill patients, and a significant bacterial culture of a endtotracheal aspirate or bronchoalveolar lavage specimen. Current guidelines for the management of VAP strongly recommend the use of early, appropriate empirical antibiotic therapy based on patient risk factors for multidrug-resistant pathogens. An alternative model focused on VAT, using serial surveillance of endotracheal aspirate specimens to identify multidrug-resistant pathogens and their antibiotic susceptibilities, would allow earlier, targeted antibiotic treatment that could improve outcomes in patients, prevent VAP, and provide an attractive model for clinical research trials.

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