Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration
Epileptic encephalopathies (EE) are characterized by severe drug-resistant seizures, early onset, and unfavorable developmental outcomes. This article discusses the use of intravenous methylprednisolone (IVMP) pulse therapy in pediatric patients with EE to evaluate its efficacy and tolerability. Thi...
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description | Epileptic encephalopathies (EE) are characterized by severe drug-resistant seizures, early onset, and unfavorable developmental outcomes. This article discusses the use of intravenous methylprednisolone (IVMP) pulse therapy in pediatric patients with EE to evaluate its efficacy and tolerability.
This is a retrospective study from 2020 to 2023. Inclusion criteria were ≤18 years at the time of IVMP pulse therapy and at least 6 months of follow-up. Efficacy and outcome, defined as seizure reduction > 50% (responder rate), were evaluated at 6 and 9 months of therapy, and 6 months after therapy suspension; quality of life (QoL) was also assessed. Variables predicting positive post-IVMP outcomes were identified using statistical analysis.
The study included 21 patients, with a responder rate of 85.7% at 6 and 9 months of therapy, and 80.9% at 6 months after therapy suspension. Variables significantly predicting favorable outcome were etiology (
= 0.0475) and epilepsy type (
= 0.0475), with the best outcome achieved in patients with genetic epilepsy and those with encephalopathy related to electrical status epilepticus during slow-wave sleep (ESES). All patients evidenced improvements in QoL at the last follow-up, with no relevant adverse events reported.
: Our study confirmed the efficacy and high tolerability of IVMP pulse therapy in pediatric patients with EE. Genetic epilepsy and ESES were positive predictors of a favorable clinical outcome. QOL, EEG tracing, and postural-motor development showed an improving trend as well. IVMP pulse therapy should be considered earlier in patients with EE. |
doi_str_mv | 10.3390/jcm13092497 |
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This is a retrospective study from 2020 to 2023. Inclusion criteria were ≤18 years at the time of IVMP pulse therapy and at least 6 months of follow-up. Efficacy and outcome, defined as seizure reduction > 50% (responder rate), were evaluated at 6 and 9 months of therapy, and 6 months after therapy suspension; quality of life (QoL) was also assessed. Variables predicting positive post-IVMP outcomes were identified using statistical analysis.
The study included 21 patients, with a responder rate of 85.7% at 6 and 9 months of therapy, and 80.9% at 6 months after therapy suspension. Variables significantly predicting favorable outcome were etiology (
= 0.0475) and epilepsy type (
= 0.0475), with the best outcome achieved in patients with genetic epilepsy and those with encephalopathy related to electrical status epilepticus during slow-wave sleep (ESES). All patients evidenced improvements in QoL at the last follow-up, with no relevant adverse events reported.
: Our study confirmed the efficacy and high tolerability of IVMP pulse therapy in pediatric patients with EE. Genetic epilepsy and ESES were positive predictors of a favorable clinical outcome. QOL, EEG tracing, and postural-motor development showed an improving trend as well. IVMP pulse therapy should be considered earlier in patients with EE.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm13092497</identifier><identifier>PMID: 38731025</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Analysis ; Caregivers ; Children ; Clinical medicine ; Convulsions & seizures ; Corticosteroids ; Development and progression ; Dosage and administration ; Drug resistance ; Drug therapy ; Electroencephalography ; Encephalopathy ; Epilepsy ; Epilepsy in children ; Health aspects ; Intravenous therapy ; Johnson, Al ; Medical research ; Medicine, Experimental ; Methods ; Methylprednisolone ; Neuropsychology ; Patient outcomes ; Pediatric research ; Pediatrics ; Performance evaluation ; Seizures (Medicine) ; Statistical analysis ; Steroids ; Variables</subject><ispartof>Journal of clinical medicine, 2024-05, Vol.13 (9), p.2497</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c379t-a0366117750f95bff5d93e99a588c43445f61224e92be0a183cb0c36b0af58df3</cites><orcidid>0000-0003-0175-6486 ; 0000-0002-1367-6419</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38731025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Russo, Angelo</creatorcontrib><creatorcontrib>Mazzone, Serena</creatorcontrib><creatorcontrib>Landolina, Laura</creatorcontrib><creatorcontrib>Colucci, Roberta</creatorcontrib><creatorcontrib>Baccari, Flavia</creatorcontrib><creatorcontrib>Fetta, Anna</creatorcontrib><creatorcontrib>Boni, Antonella</creatorcontrib><creatorcontrib>Cordelli, Duccio Maria</creatorcontrib><title>Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>Epileptic encephalopathies (EE) are characterized by severe drug-resistant seizures, early onset, and unfavorable developmental outcomes. This article discusses the use of intravenous methylprednisolone (IVMP) pulse therapy in pediatric patients with EE to evaluate its efficacy and tolerability.
This is a retrospective study from 2020 to 2023. Inclusion criteria were ≤18 years at the time of IVMP pulse therapy and at least 6 months of follow-up. Efficacy and outcome, defined as seizure reduction > 50% (responder rate), were evaluated at 6 and 9 months of therapy, and 6 months after therapy suspension; quality of life (QoL) was also assessed. Variables predicting positive post-IVMP outcomes were identified using statistical analysis.
The study included 21 patients, with a responder rate of 85.7% at 6 and 9 months of therapy, and 80.9% at 6 months after therapy suspension. Variables significantly predicting favorable outcome were etiology (
= 0.0475) and epilepsy type (
= 0.0475), with the best outcome achieved in patients with genetic epilepsy and those with encephalopathy related to electrical status epilepticus during slow-wave sleep (ESES). All patients evidenced improvements in QoL at the last follow-up, with no relevant adverse events reported.
: Our study confirmed the efficacy and high tolerability of IVMP pulse therapy in pediatric patients with EE. Genetic epilepsy and ESES were positive predictors of a favorable clinical outcome. QOL, EEG tracing, and postural-motor development showed an improving trend as well. IVMP pulse therapy should be considered earlier in patients with EE.</description><subject>Analysis</subject><subject>Caregivers</subject><subject>Children</subject><subject>Clinical medicine</subject><subject>Convulsions & seizures</subject><subject>Corticosteroids</subject><subject>Development and progression</subject><subject>Dosage and administration</subject><subject>Drug resistance</subject><subject>Drug therapy</subject><subject>Electroencephalography</subject><subject>Encephalopathy</subject><subject>Epilepsy</subject><subject>Epilepsy in children</subject><subject>Health aspects</subject><subject>Intravenous therapy</subject><subject>Johnson, Al</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Methods</subject><subject>Methylprednisolone</subject><subject>Neuropsychology</subject><subject>Patient outcomes</subject><subject>Pediatric research</subject><subject>Pediatrics</subject><subject>Performance evaluation</subject><subject>Seizures (Medicine)</subject><subject>Statistical analysis</subject><subject>Steroids</subject><subject>Variables</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkU1v1DAQhiNERau2J-7IEhcktMWO7djmVq2WUqmUSpRz5DjjrpfEDrYD2j_Q3423LVAqxoeZwzMfft-qeknwCaUKv9uYkVCsaqbEs-qgxkIsMJX0-aN6vzpOaYNLSMlqIl5U-1QKSnDND6rblbXOaLNF2vfoi7aQtyhYdDUPCdC5z1H_AB_mhD5BXm-HKULvXQpD8ICcR1fQO52jM2g1uQGmvKu8gWmthzDpvHaQ3qNrNzp_c7fiEvLPEL8ltAw-uR6izi74o2rP6rLx-CEfVl8_rK6XHxcXn8_Ol6cXC0OFyguNadMQIgTHVvHOWt4rCkppLqVhlDFuG1LXDFTdAdZEUtNhQ5sOa8tlb-lh9eZ-7hTD9xlSbkeXDAyD9lA-2VLMqRKSSVrQ10_QTZijL9fdUYQxJZu_1I0eoHXehqKY2Q1tT4WivGGKi0Kd_Icqr4fRmSKlLdr92_D2vsHEkFIE207RjTpuW4LbnfHtI-ML_erh1Lkbof_D_raZ_gID5ag_</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Russo, Angelo</creator><creator>Mazzone, Serena</creator><creator>Landolina, Laura</creator><creator>Colucci, Roberta</creator><creator>Baccari, Flavia</creator><creator>Fetta, Anna</creator><creator>Boni, Antonella</creator><creator>Cordelli, Duccio Maria</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0175-6486</orcidid><orcidid>https://orcid.org/0000-0002-1367-6419</orcidid></search><sort><creationdate>20240501</creationdate><title>Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration</title><author>Russo, Angelo ; 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This article discusses the use of intravenous methylprednisolone (IVMP) pulse therapy in pediatric patients with EE to evaluate its efficacy and tolerability.
This is a retrospective study from 2020 to 2023. Inclusion criteria were ≤18 years at the time of IVMP pulse therapy and at least 6 months of follow-up. Efficacy and outcome, defined as seizure reduction > 50% (responder rate), were evaluated at 6 and 9 months of therapy, and 6 months after therapy suspension; quality of life (QoL) was also assessed. Variables predicting positive post-IVMP outcomes were identified using statistical analysis.
The study included 21 patients, with a responder rate of 85.7% at 6 and 9 months of therapy, and 80.9% at 6 months after therapy suspension. Variables significantly predicting favorable outcome were etiology (
= 0.0475) and epilepsy type (
= 0.0475), with the best outcome achieved in patients with genetic epilepsy and those with encephalopathy related to electrical status epilepticus during slow-wave sleep (ESES). All patients evidenced improvements in QoL at the last follow-up, with no relevant adverse events reported.
: Our study confirmed the efficacy and high tolerability of IVMP pulse therapy in pediatric patients with EE. Genetic epilepsy and ESES were positive predictors of a favorable clinical outcome. QOL, EEG tracing, and postural-motor development showed an improving trend as well. IVMP pulse therapy should be considered earlier in patients with EE.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38731025</pmid><doi>10.3390/jcm13092497</doi><orcidid>https://orcid.org/0000-0003-0175-6486</orcidid><orcidid>https://orcid.org/0000-0002-1367-6419</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Caregivers Children Clinical medicine Convulsions & seizures Corticosteroids Development and progression Dosage and administration Drug resistance Drug therapy Electroencephalography Encephalopathy Epilepsy Epilepsy in children Health aspects Intravenous therapy Johnson, Al Medical research Medicine, Experimental Methods Methylprednisolone Neuropsychology Patient outcomes Pediatric research Pediatrics Performance evaluation Seizures (Medicine) Statistical analysis Steroids Variables |
title | Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration |
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