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Quality assessment and response to less invasive surfactant administration (LISA) without sedation
BACKGROUND: Although sedative premedication for endotracheal intubation is considered standard of care, less invasive surfactant administration (LISA) is often performed without sedative premedication. The aim of this study was to assess success rates, technical quality and vital parameters in LISA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223491/ https://www.ncbi.nlm.nih.gov/pubmed/31450233 http://dx.doi.org/10.1038/s41390-019-0552-z |
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author | de Kort, Ellen Kusters, Suzanne Niemarkt, Hendrik van Pul, Carola Reiss, Irwin Simons, Sinno Andriessen, Peter |
author_facet | de Kort, Ellen Kusters, Suzanne Niemarkt, Hendrik van Pul, Carola Reiss, Irwin Simons, Sinno Andriessen, Peter |
author_sort | de Kort, Ellen |
collection | PubMed |
description | BACKGROUND: Although sedative premedication for endotracheal intubation is considered standard of care, less invasive surfactant administration (LISA) is often performed without sedative premedication. The aim of this study was to assess success rates, technical quality and vital parameters in LISA without sedative premedication. METHODS: Prospective observational study in 86 neonates <32 weeks’ gestation. LISA was performed according to a standardized protocol without use of sedative premedication. Outcome measures were success rates of LISA attempts, reasons for failure and quality of technical conditions. In 37 neonates, heart rate and oxygen saturation levels from 20 min before until 30 min after start of LISA were collected. RESULTS: In 48% of LISAs the first attempt failed and in 34% quality of technical conditions was inadequate. The success rate was significantly correlated with quality of technical conditions and experience of the performer. Desaturations <80% occurred in 54% of patients while bradycardia <80/min did not occur. CONCLUSION: This study shows a relatively low success rate of the first attempt of LISA, frequent inadequacy of technical quality and frequent oxygen desaturations. These effects may be improved by the use of sedative premedication. |
format | Online Article Text |
id | pubmed-7223491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-72234912020-05-15 Quality assessment and response to less invasive surfactant administration (LISA) without sedation de Kort, Ellen Kusters, Suzanne Niemarkt, Hendrik van Pul, Carola Reiss, Irwin Simons, Sinno Andriessen, Peter Pediatr Res Clinical Research Article BACKGROUND: Although sedative premedication for endotracheal intubation is considered standard of care, less invasive surfactant administration (LISA) is often performed without sedative premedication. The aim of this study was to assess success rates, technical quality and vital parameters in LISA without sedative premedication. METHODS: Prospective observational study in 86 neonates <32 weeks’ gestation. LISA was performed according to a standardized protocol without use of sedative premedication. Outcome measures were success rates of LISA attempts, reasons for failure and quality of technical conditions. In 37 neonates, heart rate and oxygen saturation levels from 20 min before until 30 min after start of LISA were collected. RESULTS: In 48% of LISAs the first attempt failed and in 34% quality of technical conditions was inadequate. The success rate was significantly correlated with quality of technical conditions and experience of the performer. Desaturations <80% occurred in 54% of patients while bradycardia <80/min did not occur. CONCLUSION: This study shows a relatively low success rate of the first attempt of LISA, frequent inadequacy of technical quality and frequent oxygen desaturations. These effects may be improved by the use of sedative premedication. Nature Publishing Group US 2019-08-27 2020 /pmc/articles/PMC7223491/ /pubmed/31450233 http://dx.doi.org/10.1038/s41390-019-0552-z Text en © International Pediatric Research Foundation, Inc 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Clinical Research Article de Kort, Ellen Kusters, Suzanne Niemarkt, Hendrik van Pul, Carola Reiss, Irwin Simons, Sinno Andriessen, Peter Quality assessment and response to less invasive surfactant administration (LISA) without sedation |
title | Quality assessment and response to less invasive surfactant administration (LISA) without sedation |
title_full | Quality assessment and response to less invasive surfactant administration (LISA) without sedation |
title_fullStr | Quality assessment and response to less invasive surfactant administration (LISA) without sedation |
title_full_unstemmed | Quality assessment and response to less invasive surfactant administration (LISA) without sedation |
title_short | Quality assessment and response to less invasive surfactant administration (LISA) without sedation |
title_sort | quality assessment and response to less invasive surfactant administration (lisa) without sedation |
topic | Clinical Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223491/ https://www.ncbi.nlm.nih.gov/pubmed/31450233 http://dx.doi.org/10.1038/s41390-019-0552-z |
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