In vitro evaluation of radio-labeled aerosol delivery via a variable-flow infant CPAP system

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Abstract

Background: Nasal CPAP is widely used in neonatal ICUs. Aerosolized medications such as inhaled steroids and β agonists are commonly administered in-line through nasal CPAP, especially to infants with bronchopulmonary dysplasia. We hypothesized that aerosol delivery to the lungs via variable-flow nasal CPAP in an in vitro model would be unreliable, and that the delivery would depend on the position of the aerosol generator within the nasal CPAP circuit. Methods: We used a system that employed a test lung placed in a plastic jar and subjected to negative pressure. Simulated inspiration effort was measured with a heated-wire anemometer. We used technetium-99m-labeled diethylene triamine penta-acetic acid as our aerosol. The nebulizer was placed either close to the humidifier or close to the nasal prongs in the circuit, and patient effort was simulated with a minute ventilation of 0.4 L/min. Results: Relative aerosol delivery to the infant test lung with the nebulizer close to the humidifier was extremely low (0.3 ± 0.4%), whereas placing the nebulizer close to the nasal prongs resulted in significantly (P

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Farney, K. D., Kuehne, B. T., Gibson, L. A., Nelin, L. D., & Shepherd, E. G. (2014). In vitro evaluation of radio-labeled aerosol delivery via a variable-flow infant CPAP system. Respiratory Care, 59(3), 340–344. https://doi.org/10.4187/respcare.01904

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