Epilepsy in children with tuberous sclerosis complex: Chance of remission and response to antiepileptic drugs

被引:103
作者
Overwater, Iris E. [1 ,2 ]
Bindels-de Heus, Karen [2 ,3 ]
Rietman, Andre B. [1 ,2 ]
ten Hoopen, Leontine W. [2 ,4 ]
Vergouwe, Yvonne [5 ]
Moll, Henriette A. [3 ]
de Wit, Marie-Claire Y. [1 ,2 ]
机构
[1] Erasmus MC Sophia Childrens Hosp, Dept Neurol, NL-3000 CB Rotterdam, Netherlands
[2] Erasmus MC Sophia Childrens Hosp, ENCORE TSC Expertise Ctr, NL-3000 CB Rotterdam, Netherlands
[3] Erasmus MC Sophia Childrens Hosp, Dept Pediat, NL-3000 CB Rotterdam, Netherlands
[4] Erasmus MC Sophia Childrens Hosp, Dept Child & Adolescent Psychiat Psychol, NL-3000 CB Rotterdam, Netherlands
[5] Erasmus MC, Dept Publ Hlth, Rotterdam, Netherlands
关键词
Anticonvulsants; Infantile spasms; Intellectual disability; INFANTILE SPASMS; ONSET; SEIZURES; THERAPY; MULTICENTER; EVEROLIMUS; EFFICACY; TSC;
D O I
10.1111/epi.13050
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
ObjectiveTo describe treatment and outcome of epilepsy in children with tuberous sclerosis complex (TSC). MethodsSeventy-one children with TSC and epilepsy treated at the ENCORE TSC Expertise Center between 1988 and 2014 were included. Patient characteristics and duration and effectiveness of antiepileptic treatments were extracted from our clinical database. Correlations were made between recurrence of seizures after response to treatment, and several patient characteristics. ResultsMedian age at time of inclusion was 9.4years (range 0.9-18.0). Seizure history showed that 55 children (77%) of 71 became seizure-free for longer than 1month, and 21 (30%) of 71 for longer than 24months. Remission of seizures was associated with higher IQ, and a trend was observed between seizure remission and age at onset of seizures. A total of 19 antiepileptic drugs (AEDs) were used. Valproic acid, vigabatrin, levetiracetam, and carbamazepine were used most frequently. Nonpharmacologic therapies (ketogenic diet, epilepsy surgery, and vagus nerve stimulation) were used 13 times. Epilepsy surgery was most effective, with four of five children becoming seizure-free. AEDs prescribed as first and second treatment were most effective. Valproic acid was prescribed most frequently as first and second treatment, followed by vigabatrin. Thirty-one children had infantile spasms, preceded by focal seizures in 18 children (58%). Vigabatrin was used by 29 children (94%), and was first treatment in 15 (48%). Vigabatrin was more effective than other AEDs when prescribed as first treatment. SignificanceWe showed that, although 77% of children with epilepsy due to TSC reached seizure remission, usually after their first or second AED, this was sustained for at least 24months in only 38%. Almost half of those with 24 months of remission later had relapse of seizures. Our results support vigabatrin as first choice drug, and show the need for better treatment options for these children.
引用
收藏
页码:1239 / 1245
页数:7
相关论文
共 29 条
[1]
TORC1-Dependent Epilepsy Caused by Acute Biallelic Tsc1 Deletion in Adult Mice [J].
Abs, Elisabeth ;
Goorden, Susanna M. I. ;
Schreiber, Jadwiga ;
Overwater, Iris E. ;
Hoogeveen-Westerveld, Marianne ;
Bruinsma, Caroline F. ;
Aganovic, Elvedin ;
Borgesius, Nils Z. ;
Nellist, Mark ;
Elgersma, Ype .
ANNALS OF NEUROLOGY, 2013, 74 (04) :569-579
[2]
Multimodality imaging for improved detection of epileptogenic foci in tuberous sclerosis complex [J].
Asano, E ;
Chugani, DC ;
Muzik, O ;
Shen, C ;
Juhász, C ;
Janisse, J ;
Ager, J ;
Canady, A ;
Shah, JR ;
Shah, AK ;
Watson, C ;
Chugani, HT .
NEUROLOGY, 2000, 54 (10) :1976-1984
[3]
Everolimus for angiomyolipoma associated with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis (EXIST-2): a multicentre, randomised, double-blind, placebo-controlled trial [J].
Bissler, John J. ;
Kingswood, J. Christopher ;
Radzikowska, Elzbieta ;
Zonnenberg, Bernard A. ;
Frost, Michael ;
Belousova, Elena ;
Sauter, Matthias ;
Nonomura, Norio ;
Brakemeier, Susanne ;
de Vries, Petrus J. ;
Whittemore, Vicky H. ;
Chen, David ;
Sahmoud, Tarek ;
Shah, Gaurav ;
Lincy, Jeremie ;
Lebwohl, David ;
Budde, Klemens .
LANCET, 2013, 381 (9869) :817-824
[4]
Early control of seizures improves long-term outcome in children with tuberous sclerosis complex [J].
Bombardieri, Roberta ;
Pinci, Mariangela ;
Moavero, Romina ;
Cerminara, Caterina ;
Curatolo, Paolo .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2010, 14 (02) :146-149
[5]
The natural history of epilepsy in tuberous sclerosis complex [J].
Chu-Shore, Catherine J. ;
Major, Philippe ;
Camposano, Susana ;
Muzykewicz, David ;
Thiele, Elizabeth A. .
EPILEPSIA, 2010, 51 (07) :1236-1241
[6]
Levetiracetam as adjunctive antiepileptic therapy for patients with tuberous sclerosis complex: A retrospective open-label trial [J].
Collins, James J. ;
Tudor, Cynthia ;
Leonard, Jennifer M. ;
Chuck, Gail ;
Franz, David Neal .
JOURNAL OF CHILD NEUROLOGY, 2006, 21 (01) :53-57
[7]
The tuberous sclerosis complex [J].
Crino, Peter B. ;
Nathanson, Katherine L. ;
Henske, Elizabeth Petri .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (13) :1345-1356
[8]
Management of epilepsy associated with tuberous sclerosis complex (TSC): Clinical recommendations [J].
Curatolo, Paolo ;
Jozwiak, Sergiusz ;
Nabbout, Rima .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2012, 16 (06) :582-586
[9]
Long-term neurological outcome in children with early-onset epilepsy associated with tuberous sclerosis [J].
Cusmai, Raffaella ;
Moavero, Romina ;
Bombardieri, Roberta ;
Vigevano, Federico ;
Curatolo, Paolo .
EPILEPSY & BEHAVIOR, 2011, 22 (04) :735-739
[10]
EEG abnormalities preceding the epilepsy onset in tuberous sclerosis complex patients - A prospective study of 5 patients [J].
Domanska-Pakiela, D. ;
Kaczorowska, M. ;
Jurkiewicz, E. ;
Kotulska, K. ;
Dunin-Wasowicz, D. ;
Jozwiak, S. .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2014, 18 (04) :458-468