Deposition studies of aerosol delivery by nasal cannula to infants.


Journal

Pediatric pulmonology
ISSN: 1099-0496
Titre abrégé: Pediatr Pulmonol
Pays: United States
ID NLM: 8510590

Informations de publication

Date de publication:
08 2019
Historique:
received: 14 11 2018
revised: 05 03 2019
accepted: 12 03 2019
pubmed: 2 4 2019
medline: 24 3 2020
entrez: 2 4 2019
Statut: ppublish

Résumé

Nasal cannulas are used to provide oxygen support for infants and have been considered as a means for delivering aerosols to the lungs. To measure mucociliary clearance in the lungs of infants with congenital heart defects, we delivered radiopharmaceutical aerosols via a nasal cannula. Here we report on the pulmonary and nasal deposition of these aerosols. A total of 18 infants (median age = 26 days; quartiles = 11-74 days) performed clearance measurements soon before or after corrective cardiac surgery. The regional aerosol deposition was assessed using gamma camera imaging. Cannula flow rate significantly affected pulmonary dosing. Flow rates useful for oxygen support were associated with low pulmonary deposition (2 L/min; mean, 4.5% of deposited dose; range, 2%-9%; n = 7) and high nasal deposition. Much lower cannula flow rates increased the pulmonary deposition (0.2 L/min; mean, 33.5% of deposited dose; range, 15%-51%; n = 5; P = 0.005 vs 2 L/min). The ratio of nose/lung dosing was approximately 26:1 at 2 L/min and 2:1 at 0.2 L/min. Bench studies demonstrated cannula output rates of 10.2 ± 1.7% (2 L/min) and 3.3 ± 0.4% (0.2 L/min) of the loaded nebulizer dose during a 2-minute delivery. Combining in vitro and in vivo results, we estimate that 0.46% of the loaded nebulizer dose reaches the lungs at 2 L/min vs 1.10% at 0.2 L/min during a 2-minute delivery. With the delivery system used here, pulmonary aerosol delivery via nasal cannula was very inefficient at the flow rates required to provide oxygen support. Even at low flows, nasal deposition was substantial and local toxicity must be considered.

Identifiants

pubmed: 30932345
doi: 10.1002/ppul.24326
doi:

Substances chimiques

Aerosols 0
Oxygen S88TT14065

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1319-1325

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Timothy E Corcoran (TE)

Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Chemical and Petroleum Engineering Department, University of Pittsburgh, Pittsburgh, Pennsylvania.
Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.

Al Saville (A)

Respiratory Department, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

Phillip S Adams (PS)

Department of Anesthesiology and Perioperative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Darragh J Johnston (DJ)

Chemical and Petroleum Engineering Department, University of Pittsburgh, Pittsburgh, Pennsylvania.

Michael R Czachowski (MR)

Nuclear Medicine Department, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

Yuliya A Domnina (YA)

Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Jiuann-Huey Lin (JH)

Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Daniel J Weiner (DJ)

Pediatric Pulmonary Medicine, Allergy, and Immunology, University of Pittsburgh, Pittsburgh, Pennsylvania.

Alex S Huber (AS)

Chemical and Petroleum Engineering Department, University of Pittsburgh, Pittsburgh, Pennsylvania.

Joan Sanchez De Toledo (J)

Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Cecilia W Lo (CW)

Department of Developmental Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.

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