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Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy
OBJECTIVE: To define similarities and differences between neonatal arterial ischemic stroke (NAIS) and hypoxic‐ischemic neonatal encephalopathy (HINE). METHODS: A retrospective case‐control study was conducted of neonates born at 35 weeks or more and weighing 1800 g or more at a tertiary care univer...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290624/ https://www.ncbi.nlm.nih.gov/pubmed/34101180 http://dx.doi.org/10.1002/ijgo.13781 |
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author | Lambicchi, Laura Ornaghi, Sara Dal Molin, Giulia Paterlini, Giuseppe Bernasconi, Davide P. Moltrasio, Francesca Vergani, Patrizia |
author_facet | Lambicchi, Laura Ornaghi, Sara Dal Molin, Giulia Paterlini, Giuseppe Bernasconi, Davide P. Moltrasio, Francesca Vergani, Patrizia |
author_sort | Lambicchi, Laura |
collection | PubMed |
description | OBJECTIVE: To define similarities and differences between neonatal arterial ischemic stroke (NAIS) and hypoxic‐ischemic neonatal encephalopathy (HINE). METHODS: A retrospective case‐control study was conducted of neonates born at 35 weeks or more and weighing 1800 g or more at a tertiary care university hospital, between 2005 and 2016, with NAIS (group A), perinatal asphyxia (PA) with Stage II–III HINE (group B), and PA with or without Stage I HINE (group C). Ante‐ and intrapartum data, neonatal characteristics, and placental histopathology were compared. RESULTS: Eleven neonates were identified in group A, 10 in group B, and 227 in group C. Sentinel events occurred exclusively in groups B (80%) and C (41.4%). Umbilical cord blood gas values and Apgar score were worse in groups B and C compared to group A. No group A neonates required resuscitation at birth, whereas all group B and one‐third of group C neonates did. Seizures developed only in neonates in groups A and B. One neonatal death occurred in group A. There were no significant differences in placental histopathology. CONCLUSION: NAIS and PA/HINE cases have different intrapartum and neonatal features. PA does not seem necessary for the occurrence of NAIS. More research is needed regarding associated placental abnormalities. |
format | Online Article Text |
id | pubmed-9290624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92906242022-07-20 Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy Lambicchi, Laura Ornaghi, Sara Dal Molin, Giulia Paterlini, Giuseppe Bernasconi, Davide P. Moltrasio, Francesca Vergani, Patrizia Int J Gynaecol Obstet Clinical Articles OBJECTIVE: To define similarities and differences between neonatal arterial ischemic stroke (NAIS) and hypoxic‐ischemic neonatal encephalopathy (HINE). METHODS: A retrospective case‐control study was conducted of neonates born at 35 weeks or more and weighing 1800 g or more at a tertiary care university hospital, between 2005 and 2016, with NAIS (group A), perinatal asphyxia (PA) with Stage II–III HINE (group B), and PA with or without Stage I HINE (group C). Ante‐ and intrapartum data, neonatal characteristics, and placental histopathology were compared. RESULTS: Eleven neonates were identified in group A, 10 in group B, and 227 in group C. Sentinel events occurred exclusively in groups B (80%) and C (41.4%). Umbilical cord blood gas values and Apgar score were worse in groups B and C compared to group A. No group A neonates required resuscitation at birth, whereas all group B and one‐third of group C neonates did. Seizures developed only in neonates in groups A and B. One neonatal death occurred in group A. There were no significant differences in placental histopathology. CONCLUSION: NAIS and PA/HINE cases have different intrapartum and neonatal features. PA does not seem necessary for the occurrence of NAIS. More research is needed regarding associated placental abnormalities. John Wiley and Sons Inc. 2021-06-22 2022-05 /pmc/articles/PMC9290624/ /pubmed/34101180 http://dx.doi.org/10.1002/ijgo.13781 Text en © 2021 The Authors. International Journal of Gynecology & Obstetrics published by John Wiley & Sons Ltd on behalf of International Federation of Gynecology and Obstetrics https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Clinical Articles Lambicchi, Laura Ornaghi, Sara Dal Molin, Giulia Paterlini, Giuseppe Bernasconi, Davide P. Moltrasio, Francesca Vergani, Patrizia Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
title | Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
title_full | Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
title_fullStr | Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
title_full_unstemmed | Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
title_short | Different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
title_sort | different antecedents and neonatal condition in neonatal arterial ischemic stroke and hypoxic‐ischemic neonatal encephalopathy |
topic | Clinical Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290624/ https://www.ncbi.nlm.nih.gov/pubmed/34101180 http://dx.doi.org/10.1002/ijgo.13781 |
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