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Published on: July 2, 2013
Aerosol polymyxin and pneumonia in seriously ill patients
Abstract:
Pneumonia caused by Pseudomonas aeruginosa occurs frequently in critically ill patients and is associated with a mortality rate of 70 per cent. An aerosol of polymyxin B was administered (2.5 mg per kilogram per day) to the upper airways of 292 patients in a respiratory-surgical intensive-care unit during a seven-month period, in an attempt to prevent Ps. aeruginosa pneumonia. Although only one of the patients studied acquired pneumonia due to Ps. aeruginosa, 10 others acquired pneumonia caused by a polymysinx-resistant organism. Seven pneumonias were caused by organisms not frequently pathogenic to man (flavobacteria, serratia and Streptococcus faecalis). The mortality rate for acquired pneumonia in this study, 64 per cent, is greater than that in previous studies in which either no polymyxin or cyclic polymyxin therapy was used. Continuous use of polymyxin B aerosol appears to be a dangerous form of therapy.
Insights
Continuous polymyxin B aerosol therapy for critically ill patients did not prevent Pseudomonas aeruginosa pneumonia but led to resistant organisms and high mortality. This therapy is considered dangerous.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Pharmacology
Background:
- Pseudomonas aeruginosa pneumonia is a severe complication in critically ill patients, carrying a high mortality rate.
- Preventing ventilator-associated pneumonia (VAP) caused by multidrug-resistant organisms is a significant challenge in intensive care units.
Purpose of the Study:
- To evaluate the efficacy of aerosolized polymyxin B in preventing Pseudomonas aeruginosa pneumonia in a respiratory-surgical intensive care unit.
- To assess the safety and impact of polymyxin B aerosol on the development of resistant pathogens.
Main Methods:
- A prospective study involving 292 critically ill patients in a respiratory-surgical ICU over seven months.
- Administration of aerosolized polymyxin B (2.5 mg/kg/day) to the upper airways of patients.
- Monitoring for the development of pneumonia, causative organisms, and patient mortality.
Main Results:
- Only one case of Pseudomonas aeruginosa pneumonia occurred, suggesting prevention of this specific pathogen.
- Ten patients developed pneumonia caused by polymyxin-resistant organisms.
- Seven pneumonias were attributed to less common pathogens, including flavobacteria, serratia, and Streptococcus faecalis.
- The overall mortality rate for hospital-acquired pneumonia in the study group was 64%.
Conclusions:
- Continuous aerosolized polymyxin B is ineffective in preventing Pseudomonas aeruginosa pneumonia and may promote the emergence of resistant organisms.
- The use of polymyxin B aerosol in this context was associated with a high mortality rate, exceeding that of previous studies.
- Continuous polymyxin B aerosol therapy is considered a dangerous intervention in critically ill patients.
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