Aerosolized antibiotics in mechanically ventilated patients: Delivery and response

Objectives: To determine whether aerosolized antibiotics can be delivered efficiently to the lower respiratory tract in mechanically ventilated patients and to define possible clinical responses to these agents. Design: Prospective serial study with cases as their own control. Setting: A 10-bed respiratory care unit for patients with chronic respiratory failure in a tertiary university hospital. Patients: Ventilator dependent patients who are otherwise medically stable. All subjects had a tracheostomy in place, were colonized with Gram-negative organisms, and produced purulent secretions which could be sampled daily. Interventions: Six patients received nine courses of nebulized therapy, which consisted of treatments every 8 hrs of gentamicin (80 mg) or amikacin (400 mg) for 14 to 21 days. Measurements and Main Results: Doses to the lung were measured using radiolabeled aerosols and antibiotic concentrations in sputum. The response was assessed by a) changes in the volume of respiratory secretions; b) effect on bacterial cultures; and c) changes in the inflammatory calls end mediators of inflammation of the respiratory secretions (interleukin-1β [IL-1β], tumor necrosis factor-α [TNF-α], soluble intercellular adhesion molecule-1 [sICAM-1], and human leukocyte elastase). On average, patients inhaled 35.4 ± 5.08% (SD) of the initial drug placed in the nebulizer (neb-charge). Of this neb-charge, 9.50 ± 2.78% was found on the respirator tubing and tracheostomy tube and 21.9 ± 7.15% was actually deposited in the lungs. The remainder of the neb-charge was sequestered in the nebulizer or exhaled. Trough sputum concentrations averaged 4.3 ± 3.2 mg/mL/mg neb-charge (range 234 to 520 μg/mL) and increased to 16.6 ± 8.1 μg/mL/mg neb-charge (range 1005 to 5839 μg/mL) immediately after therapy (p = .011). Serum concentrations were undetectable in most determinations except for a single patient who was in renal failure (8.7 μg/mL amikacin). Treatment caused a significant reduction in the volume of secretions (p = .002). Weekly cultures revealed eradication of Pseudomonas species, Serratia marcescens, and Enterobacter aerogenes in most of the trials. Before antibiotic treatment, concentrations of IL-1β were higher than those reported in acute respiratory distress syndrome. Throughout the duration of the study, IL-1β correlated significantly with the absolute number of macrophages, neutrophils, and lymphocytes, respectively (r(t) = .55, p = .002; r² = .50, p < .0004, r² = .36, p = .005). TNF-α concentrations correlated with lymphocytes and neutrophils, respectively (r² = .27, p = .013, r² = .21, p = .033). sICAM- 1 concentrations increased two-fold (p < .001) during treatment and then returned to baseline. The volume of secretions was related to neutrophil and IL-1β concentrations, respectively (r² = .25, p = .008, r² = .35, p = .006). Conclusions: Nebulizer delivery of aerosolized aminoglycosides is efficient end predictable. In our clinical model, aerosolized antibiotics can make a significant impact on respiratory secretions. Their efficacy in treatment of critically ill patients remains to be determined.