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Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy
AIM: To describe early cerebral oxygenation (cSO(2)) and fractional tissue oxygen extraction (FTOE) values and their evolution over the first days of life in infants with all grades of hypoxic‐ischaemic encephalopathy (HIE) and to determine whether cSO(2) and FTOE measured early (6 and 12 h) can pre...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545024/ https://www.ncbi.nlm.nih.gov/pubmed/35869794 http://dx.doi.org/10.1111/apa.16493 |
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author | Garvey, Aisling A. O'Toole, John M. Livingstone, Vicki Walsh, Brian Moore, Michael Pavel, Andreea M. Panaite, Lavinia Ryan, Mary Anne Boylan, Geraldine B. Murray, Deirdre M. Dempsey, Eugene M. |
author_facet | Garvey, Aisling A. O'Toole, John M. Livingstone, Vicki Walsh, Brian Moore, Michael Pavel, Andreea M. Panaite, Lavinia Ryan, Mary Anne Boylan, Geraldine B. Murray, Deirdre M. Dempsey, Eugene M. |
author_sort | Garvey, Aisling A. |
collection | PubMed |
description | AIM: To describe early cerebral oxygenation (cSO(2)) and fractional tissue oxygen extraction (FTOE) values and their evolution over the first days of life in infants with all grades of hypoxic‐ischaemic encephalopathy (HIE) and to determine whether cSO(2) and FTOE measured early (6 and 12 h) can predict short‐term outcome. METHODS: Prospective, observational study of cerebral near‐infrared spectroscopy (NIRS) in infants >36 weeks' gestation with HIE. Ten one‐hour epochs of cSO(2) and FTOE were extracted for each infant over the first 84 h. Infants with moderate and severe HIE received therapeutic hypothermia (TH). Abnormal outcome was defined as abnormal magnetic resonance imaging (MRI) and/or death. RESULTS: Fifty‐eight infants were included (28 mild, 24 moderate, 6 severe). Median gestational age was 39.9 weeks (IQR 38.1–40.7) and birthweight was 3.35 kgs (IQR 2.97–3.71). cSO(2) increased and FTOE decreased over the first 24 h in all grades of HIE. Compared to the moderate group, infants with mild HIE had significantly higher cSO(2) at 6 h (p = 0.003), 9 h (p = 0.009) and 12 h (p = 0.032) and lower FTOE at 6 h (p = 0.016) and 9 h (0.029). cSO(2) and FTOE at 6 and 12 h did not predict abnormal outcome. CONCLUSION: Infants with mild HIE have higher cSO(2) and lower FTOE than those with moderate or severe HIE in the first 12 h of life. cSO(2) increased in all grades of HIE over the first 24 h regardless of TH status. |
format | Online Article Text |
id | pubmed-9545024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95450242022-10-14 Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy Garvey, Aisling A. O'Toole, John M. Livingstone, Vicki Walsh, Brian Moore, Michael Pavel, Andreea M. Panaite, Lavinia Ryan, Mary Anne Boylan, Geraldine B. Murray, Deirdre M. Dempsey, Eugene M. Acta Paediatr Original Articles & Brief Reports AIM: To describe early cerebral oxygenation (cSO(2)) and fractional tissue oxygen extraction (FTOE) values and their evolution over the first days of life in infants with all grades of hypoxic‐ischaemic encephalopathy (HIE) and to determine whether cSO(2) and FTOE measured early (6 and 12 h) can predict short‐term outcome. METHODS: Prospective, observational study of cerebral near‐infrared spectroscopy (NIRS) in infants >36 weeks' gestation with HIE. Ten one‐hour epochs of cSO(2) and FTOE were extracted for each infant over the first 84 h. Infants with moderate and severe HIE received therapeutic hypothermia (TH). Abnormal outcome was defined as abnormal magnetic resonance imaging (MRI) and/or death. RESULTS: Fifty‐eight infants were included (28 mild, 24 moderate, 6 severe). Median gestational age was 39.9 weeks (IQR 38.1–40.7) and birthweight was 3.35 kgs (IQR 2.97–3.71). cSO(2) increased and FTOE decreased over the first 24 h in all grades of HIE. Compared to the moderate group, infants with mild HIE had significantly higher cSO(2) at 6 h (p = 0.003), 9 h (p = 0.009) and 12 h (p = 0.032) and lower FTOE at 6 h (p = 0.016) and 9 h (0.029). cSO(2) and FTOE at 6 and 12 h did not predict abnormal outcome. CONCLUSION: Infants with mild HIE have higher cSO(2) and lower FTOE than those with moderate or severe HIE in the first 12 h of life. cSO(2) increased in all grades of HIE over the first 24 h regardless of TH status. John Wiley and Sons Inc. 2022-08-03 2022-10 /pmc/articles/PMC9545024/ /pubmed/35869794 http://dx.doi.org/10.1111/apa.16493 Text en © 2022 The Authors. Acta Paediatrica published by John Wiley & Sons Ltd on behalf of Foundation Acta Paediatrica. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles & Brief Reports Garvey, Aisling A. O'Toole, John M. Livingstone, Vicki Walsh, Brian Moore, Michael Pavel, Andreea M. Panaite, Lavinia Ryan, Mary Anne Boylan, Geraldine B. Murray, Deirdre M. Dempsey, Eugene M. Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy |
title | Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy |
title_full | Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy |
title_fullStr | Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy |
title_full_unstemmed | Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy |
title_short | Evolution of early cerebral NIRS in hypoxic ischaemic encephalopathy |
title_sort | evolution of early cerebral nirs in hypoxic ischaemic encephalopathy |
topic | Original Articles & Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545024/ https://www.ncbi.nlm.nih.gov/pubmed/35869794 http://dx.doi.org/10.1111/apa.16493 |
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