Literature DB >> 15279868

Modeling remission and relapse in pediatric epilepsy: application of a Markov process.

Anne T Berg1, Jianxin Lin, Nader Ebrahimi, Francine M Testa, Susan R Levy, Shlomo Shinnar.   

Abstract

Seizure outcome is frequently described in terms of patients ever attaining remission or being in terminal remission. Outcomes are more complicated and, over many years, repeated remission and relapses may occur. These are difficult to quantify with standard survival techniques used in analysis of remission and relapse. The Markov process, which allows one to track a patient's state (remission or not) over time, provides a suitable approach for studying repeated remission and relapse. In a prospective community-based study of children followed from the point of the initial diagnosis of epilepsy, we examined the probability of repeated remission and relapse over up to three different remission episodes (minimum 1 year each) per patient. The role of epilepsy syndrome was the main determinant of remission-relapse patterns considered in the analysis. Two different Markov models were used, one involving three states and the other seven states. Of 613 children initially recruited into the study, 602 were followed at least 1 year and thus eligible for the analysis. Almost 90% of the cohort experienced a remission; however, almost half then relapsed. Second remissions occurred in 81% of those who relapsed of whom 38% relapsed again. A third remission occurred in 82% of those after a second relapse of whom 58% relapsed yet again. After the first 2 years, approximately 70% of the cohort was in remission, 20% was no longer in remission having relapsed, and 10% had never been in remission. Significant differences were seen by underlying epilepsy syndrome. Children with one of the epileptic encephalopathies were least likely of all syndrome groups ever to remit. Those with symptomatic partial epilepsies were less likely to remit than children with any of the other syndromes, idiopathic partial or generalized, cryptogenic partial, and unclassified. Differences between these last groups became apparent when considering their subsequent remission and relapse histories. These differences were best seen in the seven-state model. For example, idiopathic partial epilepsies were most likely to enter remission and never relapse. By contrast, idiopathic generalized and cryptogenic partial epilepsies were more likely to remit and relapse repeatedly. The Markov approach provides an alternative to standard survival techniques for understanding remission and relapse outcomes in epilepsy. Its advantage is that it allows one to track the individuals' outcome over time even as the condition fluctuates. The technique would also be applicable in virtually any remitting-relapsing disorder.

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Year:  2004        PMID: 15279868     DOI: 10.1016/j.eplepsyres.2004.05.002

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  10 in total

1.  The natural history of seizures and neuropsychiatric symptoms in childhood epilepsy with centrotemporal spikes (CECTS).

Authors:  Erin E Ross; Sally M Stoyell; Mark A Kramer; Anne T Berg; Catherine J Chu
Journal:  Epilepsy Behav       Date:  2019-10-20       Impact factor: 2.937

2.  Complete remission of childhood-onset epilepsy: stability and prediction over two decades.

Authors:  Anne T Berg; Karen Rychlik; Susan R Levy; Francine M Testa
Journal:  Brain       Date:  2014-10-22       Impact factor: 13.501

3.  Complete remission in nonsyndromic childhood-onset epilepsy.

Authors:  Anne T Berg; Francine M Testa; Susan R Levy
Journal:  Ann Neurol       Date:  2011-06-27       Impact factor: 10.422

4.  Scalp recorded spike ripples predict seizure risk in childhood epilepsy better than spikes.

Authors:  Mark A Kramer; Lauren M Ostrowski; Daniel Y Song; Emily L Thorn; Sally M Stoyell; McKenna Parnes; Dhinakaran Chinappen; Grace Xiao; Uri T Eden; Kevin J Staley; Steven M Stufflebeam; Catherine J Chu
Journal:  Brain       Date:  2019-05-01       Impact factor: 13.501

5.  A population-based study of long-term outcomes of cryptogenic focal epilepsy in childhood: cryptogenic epilepsy is probably not symptomatic epilepsy.

Authors:  Elaine C Wirrell; Brandon R Grossardt; Elson L So; Katherine C Nickels
Journal:  Epilepsia       Date:  2011-02-14       Impact factor: 5.864

Review 6.  Computer modelling of epilepsy.

Authors:  William W Lytton
Journal:  Nat Rev Neurosci       Date:  2008-07-02       Impact factor: 34.870

7.  Long-term follow-up of a large cohort with focal epilepsy of unknown cause: deciphering their clinical and prognostic characteristics.

Authors:  Arife Çimen Atalar; Ebru Nur Vanlı-Yavuz; Ebru Yılmaz; Nerses Bebek; Betül Baykan
Journal:  J Neurol       Date:  2019-12-02       Impact factor: 4.849

Review 8.  Drug Treatment of Epilepsy Neuropsychiatric Comorbidities in Children.

Authors:  Gregory L Holmes
Journal:  Paediatr Drugs       Date:  2020-11-24       Impact factor: 3.022

9.  Beta oscillations in the sensorimotor cortex correlate with disease and remission in benign epilepsy with centrotemporal spikes.

Authors:  Dan Y Song; Sally M Stoyell; Erin E Ross; Lauren M Ostrowski; Emily L Thorn; Steven M Stufflebeam; Amy K Morgan; Britt C Emerton; Mark A Kramer; Catherine J Chu
Journal:  Brain Behav       Date:  2019-02-20       Impact factor: 2.708

10.  Long-term mortality of patients with West syndrome.

Authors:  Matti Sillanpää; Raili Riikonen; Maiju M Saarinen; Dieter Schmidt
Journal:  Epilepsia Open       Date:  2016-07-28
  10 in total

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