TY - JOUR
T1 - Initial Observations on the Effect of Repeated Surfactant Dose on Lung Volume and Ventilation in Neonatal Respiratory Distress Syndrome
AU - Kallio, Merja
AU - van der Zwaag, Anne-Sea
AU - Waldmann, Andreas D.
AU - Rahtu, Marika
AU - Miedema, Martijn
AU - Papadouri, Thalia
AU - van Kaam, Anton H.
AU - Rimensberger, Peter C.
AU - Bayford, Richard
AU - Frerichs, Inéz
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Background: Exogenous surfactant administration is an essential part of respiratory distress syndrome treatment in preterm infants. Current guidelines recommend the first dose to be given as early as possible, followed by an additional dose if symptoms persist. The effect of additional dosing on regional ventilation and lung volume has not been investigated so far. Objectives: The aim of this study was to assess changes in ventilation distribution, lung volume, and gas exchange following repeated surfactant dosing in invasively ventilated neonates. Method: Preterm infants requiring invasive ventilation and repeated surfactant treatment, and participating in the prospective observational multicenter trial "Continuous Regional Analysis Device for neonate Lung (CRADL)" were included in this analysis. Ventilation distribution, end-expiratory lung impedance (EELZ), and tidal impedance variation were determined by electrical impedance tomography together with clinical parameters before and after repeat endotracheal surfactant treatment. Results: Nine neonates (gestational age 32.7 ± 2.7 weeks, weight 1,724 ± 691 g) received an additional dose of surfactant at a median postnatal age of 33.5 h (IQR 9.1-46.6). One patient was excluded from the analysis due to simultaneous interventions confounding data analysis. Repeated surfactant dose did not significantly affect ventilation distribution. There were no significant changes in EELZ or tidal impedance variation. SpO2/FiO2 increased from 248 ± 104 to 367 ± 92 (p = 0.001), while FiO2 was reduced from 0.41 ± 0.20 to 0.27 ± 0.10 (p = 0.004). Expiratory tidal volume fell from 4.3 ± 0.6 to 3.0 ± 1.2 mL/kg (p = 0.03), while other ventilator and clinical parameters remained stable. Conclusions: Repeated surfactant dose during invasive ventilation improves oxygenation without measurable changes in EELZ or ventilation distribution.
AB - Background: Exogenous surfactant administration is an essential part of respiratory distress syndrome treatment in preterm infants. Current guidelines recommend the first dose to be given as early as possible, followed by an additional dose if symptoms persist. The effect of additional dosing on regional ventilation and lung volume has not been investigated so far. Objectives: The aim of this study was to assess changes in ventilation distribution, lung volume, and gas exchange following repeated surfactant dosing in invasively ventilated neonates. Method: Preterm infants requiring invasive ventilation and repeated surfactant treatment, and participating in the prospective observational multicenter trial "Continuous Regional Analysis Device for neonate Lung (CRADL)" were included in this analysis. Ventilation distribution, end-expiratory lung impedance (EELZ), and tidal impedance variation were determined by electrical impedance tomography together with clinical parameters before and after repeat endotracheal surfactant treatment. Results: Nine neonates (gestational age 32.7 ± 2.7 weeks, weight 1,724 ± 691 g) received an additional dose of surfactant at a median postnatal age of 33.5 h (IQR 9.1-46.6). One patient was excluded from the analysis due to simultaneous interventions confounding data analysis. Repeated surfactant dose did not significantly affect ventilation distribution. There were no significant changes in EELZ or tidal impedance variation. SpO2/FiO2 increased from 248 ± 104 to 367 ± 92 (p = 0.001), while FiO2 was reduced from 0.41 ± 0.20 to 0.27 ± 0.10 (p = 0.004). Expiratory tidal volume fell from 4.3 ± 0.6 to 3.0 ± 1.2 mL/kg (p = 0.03), while other ventilator and clinical parameters remained stable. Conclusions: Repeated surfactant dose during invasive ventilation improves oxygenation without measurable changes in EELZ or ventilation distribution.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85072219540&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/31505498
U2 - 10.1159/000502612
DO - 10.1159/000502612
M3 - Article
C2 - 31505498
VL - 116
SP - 385
EP - 389
JO - Neonatology
JF - Neonatology
SN - 1661-7800
IS - 4
ER -