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Reduction of bacterial resistance with inhaled antibiotics in the intensive care unit
Lucy B Palmer1, Gerald C Smaldone
1Pulmonary, Critical Care and Sleep Division, Department of Medicine, State University of New York at Stony Brook, Stony Brook, New York.
Rationale:
Multidrug-resistant organisms (MDRO) are the dominant airway pathogens in the intensive care unit (ICU) and present a major treatment challenge to intensivists. Aerosolized antibiotics (AA) result in airway concentrations of drug 100-fold greater than the minimal inhibitory concentration of most bacteria including MDRO. These levels, without systemic toxicity, may eradicate MDRO and reduce the pressure for selection of new resistant organisms.
Objectives:
To determine if AA effectively eradicate MDRO in the intubated patient without promoting new resistance.
Methods:
In a double-blind placebo-controlled study, critically ill intubated patients were randomized if they exhibited signs of respiratory infection (purulent secretions and Clinical Pulmonary Infection Score ≥6). Using a well-characterized aerosol delivery system, AA or saline placebo was given for 14 days or until extubation. The responsible clinician determined administration of systemic antibiotics for ventilator-associated pneumonia and any other infection.
Measurements And Main Results:
AA eradicated 26 of 27 organisms present at randomization compared with 2 of 23 organisms with placebo (P < 0.0001). AA eradicated the original resistant organism on culture and Gram stain at end of treatment in 14 out of 16 patients compared with 1 of 11 for placebo (P < 0.001). New drug resistance to AA was not seen. Compared with AA, resistance to systemic antibiotics significantly increased in placebo patients (P = 0.03). Compared with placebo, AA significantly reduced Clinical Pulmonary Infection Score (mean ± SEM, 9.3 ± 2.7 to 5.3 ± 2.6 vs. 8.0 ± 23 to 8.6 ± 2.10; P = 0.0008).
Conclusions:
In chronically intubated critically ill patients, AA successfully eradicated existing MDRO organisms and reduced the pressure from systemic agents for new respiratory resistance. Clinical trial registered with www.clinicaltrials.gov (NCT 01878643).
Insights
Aerosolized antibiotics (AA) effectively eradicated multidrug-resistant organisms (MDRO) in intubated patients. This treatment reduced resistance development compared to systemic antibiotics, improving patient outcomes.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Pulmonary Medicine
Background:
- Multidrug-resistant organisms (MDRO) are a significant challenge in intensive care units (ICUs).
- Aerosolized antibiotics (AA) achieve high airway concentrations without systemic toxicity.
- AA may offer a strategy to combat MDRO and prevent further resistance.
Purpose of the Study:
- To evaluate the efficacy of aerosolized antibiotics (AA) in eradicating MDRO in intubated patients.
- To determine if AA promotes the development of new antibiotic resistance.
- To assess the impact of AA on clinical outcomes and resistance patterns.
Main Methods:
- A double-blind, placebo-controlled study was conducted on critically ill, intubated patients with respiratory infections.
- Patients received either AA or saline placebo via a specialized delivery system for 14 days or until extubation.
- Systemic antibiotics were administered at the discretion of the clinician for ventilator-associated pneumonia or other infections.
Main Results:
- AA eradicated 26 of 27 MDROs compared to 2 of 23 with placebo (P < 0.0001).
- Existing MDROs were eradicated in 14/16 patients receiving AA versus 1/11 receiving placebo (P < 0.001).
- No new resistance to AA was observed; placebo patients showed increased resistance to systemic antibiotics (P = 0.03).
- AA significantly reduced the Clinical Pulmonary Infection Score (P = 0.0008).
Conclusions:
- Aerosolized antibiotics are effective in eradicating existing MDROs in chronically intubated, critically ill patients.
- AA reduces the selection pressure for new resistance compared to systemic antibiotic use.
- This approach offers a promising strategy for managing MDRO infections in the ICU.
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