Short-Term Outcome after Repeated Less Invasive Surfactant Administration: A Retrospective Cohort Study

Kleijkers L.M.P.a· Van Der Spil J.b· Janssen L.C.E.a· Dieleman J.P.c· Andriessen P.van Kaam A.H.b,d· Onland W.b,d· Niemarkt H.J.a

Author affiliations

aDepartment of Pediatrics, Máxima Medical Centre, Veldhoven, The Netherlands
bDepartment of Neonatology, Emma’s Children Hospital, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands
cMMC Academy, Máxima Medical Centre, Veldhoven, The Netherlands
dAmsterdam Reproduction & Development, Amsterdam, The Netherlands

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Article / Publication Details

First-Page Preview

Abstract of Original Paper

Received: April 04, 2022
Accepted: July 20, 2022
Published online: September 20, 2022

Number of Print Pages: 8
Number of Figures: 1
Number of Tables: 4

ISSN: 1661-7800 (Print)
eISSN: 1661-7819 (Online)

For additional information: https://www.karger.com/NEO

Abstract

Introduction: Less invasive surfactant administration (LISA) to preterm infants is associated with decreased risk for death or BPD. After LISA, a considerable proportion requires a second dose of surfactant because of ongoing respiratory distress syndrome, raising a clinical dilemma between intubation or performing a repeated LISA (re-LISA) procedure. We aim to assess efficacy of re-LISA in avoiding subsequent nasal continuous positive airway pressure failure (need for intubation in the first 72 h of life; CPAP-F), to identify factors associated with subsequent CPAP-F, and to compare short-term outcomes following re-LISA to surfactant retreatment by endotracheal intubation and mechanical ventilation. Methods: This was an observational retrospective study in two Dutch NICUs. Inclusion criterion was infants with gestational age <32 0/7 weeks requiring a second surfactant dose. Multivariate logistic regression analysis was performed. Results: Of 209 infants requiring second surfactant dose, 132 received re-LISA. Subsequent CPAP-F was observed in 56 (42%) infants and was associated with extreme prematurity (OR 2.6, 95% CI: 1.2–5.8) and FiO2>0.5 (OR 5.4, 95% CI: 2.0–14.7). Infants receiving re-LISA had a lower risk of death or BPD compared to infants intubated for the second surfactant dose (OR 0.4, 95% CI: 0.2–0.9). Infants with CPAP-F after re-LISA had similar outcomes compared to those intubated for second surfactant dose. Conclusion: Re-LISA is effective in reducing CPAP-F and is associated with lower risk of death or BPD compared to retreatment via an endotracheal tube. Infants failing CPAP after re-LISA have similar outcomes compared to intubated infants. These findings support the use of re-LISA in preterm infants with ongoing RDS.

© 2022 S. Karger AG, Basel

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First-Page Preview

Abstract of Original Paper

Received: April 04, 2022
Accepted: July 20, 2022
Published online: September 20, 2022

Number of Print Pages: 8
Number of Figures: 1
Number of Tables: 4

ISSN: 1661-7800 (Print)
eISSN: 1661-7819 (Online)

For additional information: https://www.karger.com/NEO

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