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Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review

BACKGROUND AND AIM: Neonatal stroke is the second cause of acute symptomatic neonatal seizures after hypoxic-ischemic encephalopathy. The aim of this systematic review is to determine which drug among those available represents the best therapeutic choice for treatment of secondary seizures due to n...

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Autores principales: Sortino, Vincenzo, Marino, Silvia, Praticò, Andrea, Criscione, Roberta, Ruggieri, Martino, Pisani, Francesco, Falsaperla, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828920/
https://www.ncbi.nlm.nih.gov/pubmed/36533757
http://dx.doi.org/10.23750/abm.v93i6.13440
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author Sortino, Vincenzo
Marino, Silvia
Praticò, Andrea
Criscione, Roberta
Ruggieri, Martino
Pisani, Francesco
Falsaperla, Raffaele
author_facet Sortino, Vincenzo
Marino, Silvia
Praticò, Andrea
Criscione, Roberta
Ruggieri, Martino
Pisani, Francesco
Falsaperla, Raffaele
author_sort Sortino, Vincenzo
collection PubMed
description BACKGROUND AND AIM: Neonatal stroke is the second cause of acute symptomatic neonatal seizures after hypoxic-ischemic encephalopathy. The aim of this systematic review is to determine which drug among those available represents the best therapeutic choice for treatment of secondary seizures due to neonatal stroke. METHODS: We performed a systematic review searching on PubMed the keywords “Neonatal”, “Stroke”, “Seizures” and “Treatment”. Search was limited only to English language with no time limit. Last literature search was done on May 30, 2022. RESULTS: We selected 5 articles involving a total of 52 full-term neonates. In 96.1% the first line treatment was phenobarbital and in 3.9% was used phenobarbital associated with midazolam from the seizure onset but in all of these cases it was necessary to introduce further medications for controlling the seizures. As second line treatment was used lidocaine (response rate of 53.3%), midazolam (response rate of 15.38%) bumetanide (response rate of 100%), and fosphenytoin (no response). As third line treatment was used lidocaine (response rate of 87.5%), Midazolam (response rate of 60%), levetiracetam and clonazepam (response rate of 100%). CONCLUSIONS: Our review shows that the use of ASMs that act throughout a gabaergic mechanism are inadequate in controlling seizures secondary to neonatal stroke in full-term newborns. Very effective seems to be lidocaine and levetiracetam with an apparent safer profile in short and long term. Bumetanide shows promising results, but they need to be confirmed by phase 3 studies. (www.actabiomedica.it)
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spelling pubmed-98289202023-01-19 Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review Sortino, Vincenzo Marino, Silvia Praticò, Andrea Criscione, Roberta Ruggieri, Martino Pisani, Francesco Falsaperla, Raffaele Acta Biomed Review BACKGROUND AND AIM: Neonatal stroke is the second cause of acute symptomatic neonatal seizures after hypoxic-ischemic encephalopathy. The aim of this systematic review is to determine which drug among those available represents the best therapeutic choice for treatment of secondary seizures due to neonatal stroke. METHODS: We performed a systematic review searching on PubMed the keywords “Neonatal”, “Stroke”, “Seizures” and “Treatment”. Search was limited only to English language with no time limit. Last literature search was done on May 30, 2022. RESULTS: We selected 5 articles involving a total of 52 full-term neonates. In 96.1% the first line treatment was phenobarbital and in 3.9% was used phenobarbital associated with midazolam from the seizure onset but in all of these cases it was necessary to introduce further medications for controlling the seizures. As second line treatment was used lidocaine (response rate of 53.3%), midazolam (response rate of 15.38%) bumetanide (response rate of 100%), and fosphenytoin (no response). As third line treatment was used lidocaine (response rate of 87.5%), Midazolam (response rate of 60%), levetiracetam and clonazepam (response rate of 100%). CONCLUSIONS: Our review shows that the use of ASMs that act throughout a gabaergic mechanism are inadequate in controlling seizures secondary to neonatal stroke in full-term newborns. Very effective seems to be lidocaine and levetiracetam with an apparent safer profile in short and long term. Bumetanide shows promising results, but they need to be confirmed by phase 3 studies. (www.actabiomedica.it) Mattioli 1885 2022 2022-12-16 /pmc/articles/PMC9828920/ /pubmed/36533757 http://dx.doi.org/10.23750/abm.v93i6.13440 Text en Copyright: © 2022 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Review
Sortino, Vincenzo
Marino, Silvia
Praticò, Andrea
Criscione, Roberta
Ruggieri, Martino
Pisani, Francesco
Falsaperla, Raffaele
Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
title Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
title_full Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
title_fullStr Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
title_full_unstemmed Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
title_short Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review
title_sort efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828920/
https://www.ncbi.nlm.nih.gov/pubmed/36533757
http://dx.doi.org/10.23750/abm.v93i6.13440
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