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Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions
BACKGROUND: We investigated the association between cerebral tissue oxygen saturation (cStO(2)) measured by near-infrared spectroscopy (NIRS) and cerebral lesions including intraventricular hemorrhage (IVH) and periventricular leukomalacia (PVL). METHODS: Preterm infants <1,500 g received continu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039301/ https://www.ncbi.nlm.nih.gov/pubmed/35498781 http://dx.doi.org/10.3389/fped.2022.809248 |
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author | Schwab, Angelika L. Mayer, Benjamin Bassler, Dirk Hummler, Helmut D. Fuchs, Hans W. Bryant, Manuel B. |
author_facet | Schwab, Angelika L. Mayer, Benjamin Bassler, Dirk Hummler, Helmut D. Fuchs, Hans W. Bryant, Manuel B. |
author_sort | Schwab, Angelika L. |
collection | PubMed |
description | BACKGROUND: We investigated the association between cerebral tissue oxygen saturation (cStO(2)) measured by near-infrared spectroscopy (NIRS) and cerebral lesions including intraventricular hemorrhage (IVH) and periventricular leukomalacia (PVL). METHODS: Preterm infants <1,500 g received continuous cStO(2) monitoring, initiated at the earliest time possible and recorded until 72 h of life. Mean cStO(2) over periods of 5, 15, 30 min and 1 h were calculated. To calculate the burden of cerebral hypoxia, we defined a moving threshold based on the 10th percentile of cStO(2) of healthy study participants and calculated the area under the threshold (AUT). cStO(2) <60% for >5 min was regarded a critical event. The study was registered on clinicaltrials.gov (ID NCT01430728, URL: https://clinicaltrials.gov/ct2/show/NCT01430728?id=NCT01430728&draw=2&rank=1). RESULTS: Of 162 infants (gestational age: mean 27.2 weeks, standard deviation 20 days; birth weight: mean 852 g, standard deviation 312 g) recorded, 24/12 (14.8%/7.4) developed any/severe IVH/PVL. Mean cStO(2) was significantly lower in infants with IVH/PVL as well as severe IVH/PVL. In addition, we observed critical events defined by mean cStO(2) over 5 min <60% in four infants with severe IVH/PVL during NIRS monitoring. AUT showed no statistically significant difference between outcome groups. CONCLUSION: These findings suggest that cStO(2) is lower in infants developing IVH/PVL. This may be related to lower oxygenation and/or perfusion and implies that cStO(2) could potentially serve as an indicator of imminent cerebral lesions. |
format | Online Article Text |
id | pubmed-9039301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90393012022-04-27 Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions Schwab, Angelika L. Mayer, Benjamin Bassler, Dirk Hummler, Helmut D. Fuchs, Hans W. Bryant, Manuel B. Front Pediatr Pediatrics BACKGROUND: We investigated the association between cerebral tissue oxygen saturation (cStO(2)) measured by near-infrared spectroscopy (NIRS) and cerebral lesions including intraventricular hemorrhage (IVH) and periventricular leukomalacia (PVL). METHODS: Preterm infants <1,500 g received continuous cStO(2) monitoring, initiated at the earliest time possible and recorded until 72 h of life. Mean cStO(2) over periods of 5, 15, 30 min and 1 h were calculated. To calculate the burden of cerebral hypoxia, we defined a moving threshold based on the 10th percentile of cStO(2) of healthy study participants and calculated the area under the threshold (AUT). cStO(2) <60% for >5 min was regarded a critical event. The study was registered on clinicaltrials.gov (ID NCT01430728, URL: https://clinicaltrials.gov/ct2/show/NCT01430728?id=NCT01430728&draw=2&rank=1). RESULTS: Of 162 infants (gestational age: mean 27.2 weeks, standard deviation 20 days; birth weight: mean 852 g, standard deviation 312 g) recorded, 24/12 (14.8%/7.4) developed any/severe IVH/PVL. Mean cStO(2) was significantly lower in infants with IVH/PVL as well as severe IVH/PVL. In addition, we observed critical events defined by mean cStO(2) over 5 min <60% in four infants with severe IVH/PVL during NIRS monitoring. AUT showed no statistically significant difference between outcome groups. CONCLUSION: These findings suggest that cStO(2) is lower in infants developing IVH/PVL. This may be related to lower oxygenation and/or perfusion and implies that cStO(2) could potentially serve as an indicator of imminent cerebral lesions. Frontiers Media S.A. 2022-04-12 /pmc/articles/PMC9039301/ /pubmed/35498781 http://dx.doi.org/10.3389/fped.2022.809248 Text en Copyright © 2022 Schwab, Mayer, Bassler, Hummler, Fuchs and Bryant. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Schwab, Angelika L. Mayer, Benjamin Bassler, Dirk Hummler, Helmut D. Fuchs, Hans W. Bryant, Manuel B. Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions |
title | Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions |
title_full | Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions |
title_fullStr | Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions |
title_full_unstemmed | Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions |
title_short | Cerebral Oxygenation in Preterm Infants Developing Cerebral Lesions |
title_sort | cerebral oxygenation in preterm infants developing cerebral lesions |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039301/ https://www.ncbi.nlm.nih.gov/pubmed/35498781 http://dx.doi.org/10.3389/fped.2022.809248 |
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