Aeration strategy at birth influences the physiological response to surfactant in preterm lambs.


Journal

Archives of disease in childhood. Fetal and neonatal edition
ISSN: 1468-2052
Titre abrégé: Arch Dis Child Fetal Neonatal Ed
Pays: England
ID NLM: 9501297

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 18 09 2018
revised: 26 11 2018
accepted: 19 12 2018
pubmed: 10 9 2019
medline: 2 11 2019
entrez: 10 9 2019
Statut: ppublish

Résumé

The influence of pressure strategies to promote lung aeration at birth on the subsequent physiological response to exogenous surfactant therapy has not been investigated. To compare the effect of sustained inflation (SI) and a dynamic positive end-expiratory pressure (PEEP) manoeuvre at birth on the subsequent physiological response to exogenous surfactant therapy in preterm lambs. Steroid-exposed preterm lambs (124-127 days' gestation; n=71) were randomly assigned from birth to either (1) positive-pressure ventilation (PPV) with no recruitment manoeuvre; (2) SI until stable aeration; or (3) 3 min dynamic stepwise PEEP strategy (maximum 14-20 cmH Compliance increased after surfactant only in the DynPEEP group (p<0.0001, repeated measures analysis of variance), being 0.17 (0.10, 0.23) mL/kg/cmH A DynPEEP strategy at birth may improve the response to early surfactant therapy, whereas rapid lung inflation with SI creates non-uniform aeration that appears to inhibit surfactant efficacy.

Sections du résumé

BACKGROUND BACKGROUND
The influence of pressure strategies to promote lung aeration at birth on the subsequent physiological response to exogenous surfactant therapy has not been investigated.
OBJECTIVES OBJECTIVE
To compare the effect of sustained inflation (SI) and a dynamic positive end-expiratory pressure (PEEP) manoeuvre at birth on the subsequent physiological response to exogenous surfactant therapy in preterm lambs.
METHODS METHODS
Steroid-exposed preterm lambs (124-127 days' gestation; n=71) were randomly assigned from birth to either (1) positive-pressure ventilation (PPV) with no recruitment manoeuvre; (2) SI until stable aeration; or (3) 3 min dynamic stepwise PEEP strategy (maximum 14-20 cmH
RESULTS RESULTS
Compliance increased after surfactant only in the DynPEEP group (p<0.0001, repeated measures analysis of variance), being 0.17 (0.10, 0.23) mL/kg/cmH
CONCLUSIONS CONCLUSIONS
A DynPEEP strategy at birth may improve the response to early surfactant therapy, whereas rapid lung inflation with SI creates non-uniform aeration that appears to inhibit surfactant efficacy.

Identifiants

pubmed: 31498776
pii: archdischild-2018-316240
doi: 10.1136/archdischild-2018-316240
doi:

Substances chimiques

Pulmonary Surfactants 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

F587-F593

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: DGT and RLD have previously received grant funding from Chiesi Farmaceutici unrelated to this study.

Auteurs

David Gerald Tingay (DG)

Neonatology, Royal Children's Hospital, Parkville, Victoria, Australia.
Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.
Neonatal Research, The Royal Women's Hospital, Parkville, Victoria, Australia.

Andrea Togo (A)

Neonatology, Royal Children's Hospital, Parkville, Victoria, Australia.

Prue M Pereira-Fantini (PM)

Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.

Martijn Miedema (M)

Neonatology, Royal Children's Hospital, Parkville, Victoria, Australia.
Neonatology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Karen E McCall (KE)

Neonatology, Royal Children's Hospital, Parkville, Victoria, Australia.
Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.

Elizabeth J Perkins (EJ)

Neonatology, Royal Children's Hospital, Parkville, Victoria, Australia.
Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.

Jessica Thomson (J)

Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.

Georgie Dowse (G)

Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.

Magdy Sourial (M)

Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.

Raffaele L Dellacà (RL)

TBM Lab, Dipartimento di Elettronica, Informazione e BioIngegneria (DEIB), Politecnico di Milano University, Milan, Italy.

Peter G Davis (PG)

Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Neonatal Research, The Royal Women's Hospital, Parkville, Victoria, Australia.
Department of Obstetrics and Gynaecology, University of Melbourne, Melbourne, Victoria, Australia.

Peter Anderson Dargaville (PA)

Neonatal Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Neonatal and Paediatric Intensive Care Unit, Royal Hobart Hospital, Hobart, Tasmania, Australia.
Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.

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Classifications MeSH