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Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes
This study evaluated the risk of brain damage in neonates delivered at <34 weeks following a prolonged latency after preterm premature rupture of membranes (pPROM). The medical records of 77 singletons delivered at <34 weeks with pPROM and 66 singletons delivered at <34 weeks with preterm l...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729956/ https://www.ncbi.nlm.nih.gov/pubmed/16778394 http://dx.doi.org/10.3346/jkms.2006.21.3.485 |
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author | Park, Su Hyun Kim, Hai Joong Yang, Jae Hyug Choi, June seek Lim, Ji Eun Oh, Min Jeong Na, Jung Yeol |
author_facet | Park, Su Hyun Kim, Hai Joong Yang, Jae Hyug Choi, June seek Lim, Ji Eun Oh, Min Jeong Na, Jung Yeol |
author_sort | Park, Su Hyun |
collection | PubMed |
description | This study evaluated the risk of brain damage in neonates delivered at <34 weeks following a prolonged latency after preterm premature rupture of membranes (pPROM). The medical records of 77 singletons delivered at <34 weeks with pPROM and 66 singletons delivered at <34 weeks with preterm labor and intact membranes were reviewed. Latency was divided into four intervals: ≤24, >24-≤72, >72-≤168 hr, and >1 week. Outcomes in the longer three intervals were compared with those in neonates delivered at ≤24 hr after pPROM. The documented outcomes were placental (histologic chorioamnionitis, vasculitis, funnisitis) and neonatal (intraventricular hemorrhage, ventriculomegaly, germinal matrix hemorrhage, periventricular leukomalacia). Odds ratios and 95% CI for the risk of histologic chorioamnionitis according to the respective latency intervals were 4.8 (1.0-22.9), 7.0 (1.1-43.1), 7.4 (2.1-42.3) in patients with pPROM. The risks of intracranial ultrasonic abnormalities, however, did not increased with prolonged latency. In the patients with preterm labor and intact membranes, the both risks did not increased with increasing latency. Therefore, this study was suggested that the risk of histologic chorioamnionitis increased with increasing latency, but there was no relationship between neonatal brain damage and latency interval after pPROM. |
format | Text |
id | pubmed-2729956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-27299562009-08-24 Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes Park, Su Hyun Kim, Hai Joong Yang, Jae Hyug Choi, June seek Lim, Ji Eun Oh, Min Jeong Na, Jung Yeol J Korean Med Sci Original Article This study evaluated the risk of brain damage in neonates delivered at <34 weeks following a prolonged latency after preterm premature rupture of membranes (pPROM). The medical records of 77 singletons delivered at <34 weeks with pPROM and 66 singletons delivered at <34 weeks with preterm labor and intact membranes were reviewed. Latency was divided into four intervals: ≤24, >24-≤72, >72-≤168 hr, and >1 week. Outcomes in the longer three intervals were compared with those in neonates delivered at ≤24 hr after pPROM. The documented outcomes were placental (histologic chorioamnionitis, vasculitis, funnisitis) and neonatal (intraventricular hemorrhage, ventriculomegaly, germinal matrix hemorrhage, periventricular leukomalacia). Odds ratios and 95% CI for the risk of histologic chorioamnionitis according to the respective latency intervals were 4.8 (1.0-22.9), 7.0 (1.1-43.1), 7.4 (2.1-42.3) in patients with pPROM. The risks of intracranial ultrasonic abnormalities, however, did not increased with prolonged latency. In the patients with preterm labor and intact membranes, the both risks did not increased with increasing latency. Therefore, this study was suggested that the risk of histologic chorioamnionitis increased with increasing latency, but there was no relationship between neonatal brain damage and latency interval after pPROM. The Korean Academy of Medical Sciences 2006-06 2006-06-21 /pmc/articles/PMC2729956/ /pubmed/16778394 http://dx.doi.org/10.3346/jkms.2006.21.3.485 Text en Copyright © 2006 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Su Hyun Kim, Hai Joong Yang, Jae Hyug Choi, June seek Lim, Ji Eun Oh, Min Jeong Na, Jung Yeol Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes |
title | Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes |
title_full | Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes |
title_fullStr | Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes |
title_full_unstemmed | Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes |
title_short | Neonatal Brain Damage Following Prolonged Latency after Preterm Premature Rupture of Membranes |
title_sort | neonatal brain damage following prolonged latency after preterm premature rupture of membranes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729956/ https://www.ncbi.nlm.nih.gov/pubmed/16778394 http://dx.doi.org/10.3346/jkms.2006.21.3.485 |
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