Bubble bilevel ventilation facilitates gas exchange in anesthetized rabbits.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
02 2021
Historique:
received: 22 01 2019
accepted: 15 04 2020
revised: 14 04 2020
pubmed: 2 5 2020
medline: 15 1 2022
entrez: 2 5 2020
Statut: ppublish

Résumé

Bubble continuous positive airway pressure is an established therapy for infants in respiratory distress. In resource-limited settings, few treatment options exist for infants requiring further respiratory support. A bubble bilevel device has been developed to provide nonelectric, time-cycled, pressure-limited respiratory support. We compared the efficacy of bubble bilevel ventilation with conventional mechanical ventilation in sedated rabbits. Six adult rabbits under inhaled isoflurane general anesthesia were ventilated by alternating intervals of conventional and bubble bilevel ventilation for three 10-15-min periods. During each period, interval arterial blood gas (ABG) measurements were obtained after at least 10 min on the respective mode of ventilation. The bubble bilevel system was able to deliver the following pressures: 20/7, 15/5, 12/5, 8/5 cm H This study demonstrates promising in vivo results on the efficacy of a novel bubble bilevel device, which may prove useful for infants in respiratory distress. Given the lack of personnel, funds or infrastructure to provide neonatal mechanical ventilation in resource-limited settings, additional low-cost, low-tech treatments are necessary to save infant lives. Bubble bilevel ventilation reliably delivers two levels of airway pressure to anesthetized rabbits resulting in normalization of blood gases comparable to those achieved on a traditional ventilator. If proven effective, simple technologies like this device have the potential to significantly impact neonatal mortality due to respiratory distress globally.

Sections du résumé

BACKGROUND
Bubble continuous positive airway pressure is an established therapy for infants in respiratory distress. In resource-limited settings, few treatment options exist for infants requiring further respiratory support. A bubble bilevel device has been developed to provide nonelectric, time-cycled, pressure-limited respiratory support. We compared the efficacy of bubble bilevel ventilation with conventional mechanical ventilation in sedated rabbits.
METHODS
Six adult rabbits under inhaled isoflurane general anesthesia were ventilated by alternating intervals of conventional and bubble bilevel ventilation for three 10-15-min periods. During each period, interval arterial blood gas (ABG) measurements were obtained after at least 10 min on the respective mode of ventilation.
RESULTS
The bubble bilevel system was able to deliver the following pressures: 20/7, 15/5, 12/5, 8/5 cm H
CONCLUSION
This study demonstrates promising in vivo results on the efficacy of a novel bubble bilevel device, which may prove useful for infants in respiratory distress.
IMPACT
Given the lack of personnel, funds or infrastructure to provide neonatal mechanical ventilation in resource-limited settings, additional low-cost, low-tech treatments are necessary to save infant lives. Bubble bilevel ventilation reliably delivers two levels of airway pressure to anesthetized rabbits resulting in normalization of blood gases comparable to those achieved on a traditional ventilator. If proven effective, simple technologies like this device have the potential to significantly impact neonatal mortality due to respiratory distress globally.

Identifiants

pubmed: 32357365
doi: 10.1038/s41390-020-0928-0
pii: 10.1038/s41390-020-0928-0
pmc: PMC7223040
doi:

Substances chimiques

Gases 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

622-627

Références

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Auteurs

Stephen C John (SC)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA. scjres@gmail.com.

Azmath Mohammed (A)

Beaumont Medical Center, Royal Oak, MI, USA.

Joseph T Church (JT)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

Anna V John (AV)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

Elena M Perkins (EM)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

Jennifer S McLeod (JS)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

Benjamin D Carr (BD)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

Sue Smith (S)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

J Hudson Barnett (JH)

Western Michigan University, Kalamazoo, MI, USA.

Peter A Gustafson (PA)

Western Michigan University, Kalamazoo, MI, USA.

Macdonald Dick (M)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

Sunil P John (SP)

C.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI, USA.

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