Many patients who need airway clearance therapies are also prescribed inhaled therapies. Different clinical scenarios include patients receiving invasive ventilatory support and others who are not. The latter group can use a positive expiratory pressure or oscillating positive expiratory pressure device that allows concurrent airway clearance and nebulization without affecting aerosol characteristics.1 These patients can also use intrapulmonary percussive ventilation (IPV).2,3 Previous studies have reported that IPV generates a submicronic aerosol and that it was an inefficient delivery device.4,5 Reychler et al4 reported that, in healthy adults, IPV produced lower lung deposition (2.5%) of a radiolabeled aerosol and had more interindividual variability (104%) than a jet nebulizer. In another study,5 investigators reported 0.8% and 5.6% intrapulmonary deposition for IPV and for a jet nebulizer, respectively, measuring urinary excretion of amikacin.
Patients receiving invasive mechanical ventilation have limited options for combined airway clearance and inhaled therapies. They could use inline aerosol administration while receiving high-frequency chest oscillation, or they could use IPV. A study using an adult model reported that superimposing IPV with conventional mechanical ventilation can result in auto-PEEP and an increase in tidal volume.6 Another study using a pediatric model with IPV reported low aerosol delivery and no difference between IPV operation in easy or hard settings.7
Information regarding the drug delivery of aerosols generated by IPV in patients receiving mechanical ventilation are limited.7 We welcome newer information to better understand how IPV can be used to deliver aerosols. In this issue of Respiratory Care, Karashima et al8 publish an in vitro study about albuterol delivery in a model of an intubated adult. The authors delivered IPV at different pressures and frequencies, of operation, and they used a model that could replicate different respiratory mechanics. They used IPV connected to the endotracheal tube but not connected to the ventilator circuit. The authors reported albuterol delivery after the endotracheal tube between 0.4% and 2% for each of the tested conditions.8
Karashima and colleagues found that the addition of the endotracheal tube resulted in a decrease in output from 2.8% to 2% (see article Fig. 1, filters A and B). They also reported that the ventilator of the phasitron lost 15.2% of the aerosol (see article Fig. 1, filter C). Unfortunately, the authors did not perform a mass balance, and 80% of the aerosol was unaccounted for. The authors reported an increase in albuterol delivery when the IPV settings were changed from easy to hard, which resulted in higher tidal volumes.8 These results contradict previous data that found no difference between the easy and hard settings in a pediatric model using IPV superimposed with conventional mechanical ventilation.7 Differences in investigational setup might explain these differences. Karashima et al8 also reported that when the respiratory mechanics were set at high resistance, albuterol delivery decreased regardless of the compliance. They also found that high peak inspiratory pressures, even up to 80 cm H2O, occurred during IPV therapy. These data are in agreement with those of Dellamonica et al6 and should serve as warning that these patients must be carefully monitored for the development of complications.
One problem with translating these findings into clinical practice is that the IPV configuration used by the authors required breaking the circuit. This practice carries 2 potential problems: increasing the risk for ventilator-associated pneumonia, and potential lung de-recruitment in patients ventilated with high PEEP.9,10 Other studies using the manufacturer's adapter, which allows the operation of the device without disconnecting the patient from the ventilator circuit, provided information that could be used for patients who are not good candidates for disconnection from the ventilator circuit.6,7
In summary, this study increases our knowledge regarding aerosol delivery with IPV in patients receiving invasive mechanical ventilation. The findings confirm that IPV provides inefficient drug delivery, and that it should be carefully used in these populations due to the reported increase in pressures that could result in the development of barotrauma.
Footnotes
- Correspondence: Ariel Berlinski MD FAARC, University of Arkansas for Medical Sciences, Department of Pediatrics, Pulmonary Medicine, 1 Children's Way, Slot 512-17, Little Rock, AR 72202. E-mail: berlinskiariel{at}uams.edu.
Dr Berlinski has disclosed relationships with Cempra Therapeutics, Mylan, Novartis, Vertex, Abbvie, Aptalis, Therapeutic Development Network, National Institutes of Health, and Trudell Medical International.
See the Original Study on Page 502
- Copyright © 2019 by Daedalus Enterprises
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