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Time to 12-month remission and treatment failure for generalised and unclassified epilepsy
OBJECTIVES: To develop prognostic models for time to 12-month remission and time to treatment failure after initiating antiepileptic drug monotherapy for generalised and unclassified epilepsy. METHODS: We analysed data from the Standard and New Antiepileptic Drug (arm B) study, a randomised trial th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033033/ https://www.ncbi.nlm.nih.gov/pubmed/24292995 http://dx.doi.org/10.1136/jnnp-2013-306040 |
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author | Bonnett, Laura J Tudur Smith, Catrin Smith, David Williamson, Paula R Chadwick, David Marson, Anthony G |
author_facet | Bonnett, Laura J Tudur Smith, Catrin Smith, David Williamson, Paula R Chadwick, David Marson, Anthony G |
author_sort | Bonnett, Laura J |
collection | PubMed |
description | OBJECTIVES: To develop prognostic models for time to 12-month remission and time to treatment failure after initiating antiepileptic drug monotherapy for generalised and unclassified epilepsy. METHODS: We analysed data from the Standard and New Antiepileptic Drug (arm B) study, a randomised trial that compared initiating treatment with lamotrigine, topiramate and valproate in patients diagnosed with generalised or unclassified epilepsy. Multivariable regression modelling was used to investigate how clinical factors affect the probability of achieving 12-month remission and treatment failure. RESULTS: Significant factors in the multivariable model for time to 12-month remission were having a relative with epilepsy, neurological insult, total number of tonic-clonic seizures before randomisation, seizure type and treatment. Significant factors in the multivariable model for time to treatment failure were treatment history (antiepileptic drug treatment prior to randomisation), EEG result, seizure type and treatment. CONCLUSIONS: The models described within this paper can be used to identify patients most likely to achieve 12-month remission and most likely to have treatment failure, aiding individual patient risk stratification and the design and analysis of future epilepsy trials. |
format | Online Article Text |
id | pubmed-4033033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40330332014-06-05 Time to 12-month remission and treatment failure for generalised and unclassified epilepsy Bonnett, Laura J Tudur Smith, Catrin Smith, David Williamson, Paula R Chadwick, David Marson, Anthony G J Neurol Neurosurg Psychiatry Epilepsy OBJECTIVES: To develop prognostic models for time to 12-month remission and time to treatment failure after initiating antiepileptic drug monotherapy for generalised and unclassified epilepsy. METHODS: We analysed data from the Standard and New Antiepileptic Drug (arm B) study, a randomised trial that compared initiating treatment with lamotrigine, topiramate and valproate in patients diagnosed with generalised or unclassified epilepsy. Multivariable regression modelling was used to investigate how clinical factors affect the probability of achieving 12-month remission and treatment failure. RESULTS: Significant factors in the multivariable model for time to 12-month remission were having a relative with epilepsy, neurological insult, total number of tonic-clonic seizures before randomisation, seizure type and treatment. Significant factors in the multivariable model for time to treatment failure were treatment history (antiepileptic drug treatment prior to randomisation), EEG result, seizure type and treatment. CONCLUSIONS: The models described within this paper can be used to identify patients most likely to achieve 12-month remission and most likely to have treatment failure, aiding individual patient risk stratification and the design and analysis of future epilepsy trials. BMJ Publishing Group 2014-06 2013-11-29 /pmc/articles/PMC4033033/ /pubmed/24292995 http://dx.doi.org/10.1136/jnnp-2013-306040 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Epilepsy Bonnett, Laura J Tudur Smith, Catrin Smith, David Williamson, Paula R Chadwick, David Marson, Anthony G Time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
title | Time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
title_full | Time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
title_fullStr | Time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
title_full_unstemmed | Time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
title_short | Time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
title_sort | time to 12-month remission and treatment failure for generalised and unclassified epilepsy |
topic | Epilepsy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033033/ https://www.ncbi.nlm.nih.gov/pubmed/24292995 http://dx.doi.org/10.1136/jnnp-2013-306040 |
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