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Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Conference summary: ventilator-associated pneumonia
1Service de Réanimation Médicale, Institut de Cardiologie, Hôpital Pitié-Salpêtrière, 43-87 bd de l'Hôpital, 75651 Paris Cedex 13, France. jean.chastre@psl.ap-hop-paris.fr
Abstract:
Ventilator-associated pneumonia (VAP), which is usually defined as an infection occurring greater than 48 hours after hospital admission in a patient requiring mechanical ventilation, is an entity that should be viewed as a subcategory of health-care-associated pneumonia, which includes any patient who was hospitalized in an acute care hospital for 2 or more days within 90 days of the infection; resided in a nursing home or long-term care facility; received recent antibiotic therapy, chemotherapy, or wound care within the past 30 days of the current infection; or attended a hospital or hemodialysis clinic. VAP is the most frequent intensive-care-unit (ICU)-acquired infection among patients receiving mechanical ventilation. In contrast to infections of other frequently involved organs (eg, urinary tract and skin), for which mortality is low, the mortality rate for VAP ranges from 20% to 50% and can reach 70% in some specific settings or when lung infection is caused by high-risk pathogens and/or when initial antibiotic therapy is inappropriate. Although the attributable mortality rate for VAP is still debated, it has been shown that these infections prolong both the duration of ventilation and the duration of ICU stay. These prolonged hospitalizations underscore the considerable financial burden imposed by the development of VAP. The causes of VAP are many and may vary by hospital, patient population, and type of ICU, emphasizing the need for timely, local surveillance data. In many cases infection is caused by multiple-drug-resistant pathogens. Risk factors for such resistant microorganisms are the duration of mechanical ventilation, prior antibiotic treatment, and contact with the health care system. Preventive measures should be guided with regard to a full understanding of pathogenesis and epidemiology. Because respiratory-tract colonization of ICU patients is generally very complex, corresponding to a mix of self-colonization and cross-transmission, only a multifaceted and multidisciplinary program can be effective. Antimicrobial therapy of patients with VAP should follow a 2-stage process. The first stage involves administering broad-spectrum antibiotics to avoid inappropriate treatment in patients with true bacterial pneumonia. The second stage focuses on trying to achieve this objective without over-using and abusing antibiotics, combining a number of different steps, such as stopping therapy in patients with a low probability of the disease, streamlining treatment once the etiologic agent is known, switching to monotherapy after days 3-5, and shortening duration of therapy to 7-8 days, as dictated by the patient's clinical response to therapy and information about the bacteriology of the infection.
Insights
Ventilator-associated pneumonia (VAP) is a common intensive-care-unit (ICU) infection with high mortality. Effective VAP management requires understanding its causes and implementing multifaceted prevention and antimicrobial therapy strategies.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Hospital Epidemiology
Background:
- Ventilator-associated pneumonia (VAP) is a frequent intensive-care-unit (ICU)-acquired infection in mechanically ventilated patients.
- VAP is a subcategory of health-care-associated pneumonia with significant mortality rates (20%-50%), potentially reaching 70%.
- It prolongs mechanical ventilation and ICU stays, imposing a considerable financial burden.
Framework:
- VAP pathogenesis and epidemiology are complex, influenced by patient-specific factors and often involving multiple-drug-resistant pathogens.
- Risk factors for resistant microorganisms include duration of mechanical ventilation, prior antibiotic use, and healthcare system contact.
- Multifaceted, multidisciplinary programs are essential for effective prevention due to complex respiratory tract colonization.
Implementation:
- Antimicrobial therapy for VAP involves a two-stage process: initial broad-spectrum antibiotics followed by de-escalation.
- Strategies include stopping therapy in low-probability cases, streamlining treatment based on identified pathogens, and switching to monotherapy.
- Shortening therapy duration to 7-8 days is guided by clinical response and bacteriology.
Implications:
- Timely, local surveillance data is crucial for guiding preventive measures and understanding VAP causes.
- Optimizing antimicrobial use is key to combating resistance while effectively treating VAP.
- A comprehensive approach integrating prevention and tailored therapy is vital for improving patient outcomes and reducing healthcare costs.
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