Epileptiform activity during rewarming from moderate cerebral hypothermia in the near-term fetal sheep
dc.contributor.author | Gerrits, LC | |
dc.contributor.author | Battin, MR | |
dc.contributor.author | Bennet, L | |
dc.contributor.author | Gonzalez, H | |
dc.contributor.author | Gunn, AJ | |
dc.date.accessioned | 2025-01-21T01:07:08Z | |
dc.date.available | 2025-01-21T01:07:08Z | |
dc.date.issued | 2005 | |
dc.description.abstract | Moderate hypothermia is consistently neuroprotective after hypoxic-ischemic insults and is the subject of ongoing clinical trials. In pilot studies, we observed rebound seizure activity in one infant during rewarming from a 72-h period of hypothermia. We therefore quantified the development of EEG-defined seizures during rewarming in an experimental paradigm of delayed cooling for cerebral ischemia. Moderate cerebral hypothermia (n = 9) or sham cooling (n = 13) was initiated 5.5 It after reperfusion from a 30-min period of bilateral carotid occlusion in near-term fetal sheep and continued for 72 h after the insult. During spontaneous rewarming, fetal extradural temperature rose from 32.5 +/- 0.6degreesC to control levels (39.4 +/- 0.1degreesC) in 47 +/- 6 min. Carotid blood flow and mean arterial blood pressure increased transiently during rewarming. The cooling group showed a significant increase in electrical seizure events 2, 3, and 5 h after rewarming, maximal at 2 h (2.9 +/- 1.2 versus 0.5 +/- 0.5 events/h; p < 0.05). From 6 h after rewarming, there was significant difference between the groups. Individual seizures were typically short (28.8 +/- 5.8 s versus 29.0 +/- 6.8 s in sham cooled; NS), and of modest amplitude (35.9 +/- 2.8 versus 38.8 +/- 3.4 muV; NS). Neuronal loss in the parasagittal cortex was significantly reduced in the cooled group (51 +/- 9% versus 91 +/- 5%; p < 0.002) and was not correlated with rebound epileptiform activity. In conclusion, rapid rewarming after a prolonged interval of therapeutic hypothermia can be associated with a transient increase in epileptiform events but does not seem to have significant adverse implications for neural outcome. | |
dc.description.funder | NICHD NIH HHS | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1203/01.PDR.0000150801.61188.5F | |
dc.identifier.eissn | 1530-0447 | |
dc.identifier.issn | 0031-3998 | |
dc.identifier.uri | https://doi.org/10.1203/01.PDR.0000150801.61188.5F | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/96282 | |
dc.identifier.wosid | WOS:000227152100006 | |
dc.issue.numero | 3 | |
dc.language.iso | en | |
dc.pagina.final | 346 | |
dc.pagina.inicio | 342 | |
dc.revista | Pediatric research | |
dc.rights | acceso restringido | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | Epileptiform activity during rewarming from moderate cerebral hypothermia in the near-term fetal sheep | |
dc.type | artículo | |
dc.volumen | 57 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |