Skip to main content
Top
Published in: Child's Nervous System 9/2011

01-09-2011 | Original Paper

Treatment of pediatric refractory status epilepticus with topiramate

Authors: Başak Nur Akyıldız, Sefer Kumandaş

Published in: Child's Nervous System | Issue 9/2011

Login to get access

Abstract

Objective

We evaluated a topiramate (TPM) regimen for treating refractory status epilepticus in the largest pediatric series, reported to date.

Methods

Fourteen patients received TPM via the nasogastric route. Initially, all patients received TPM as a 5 mg/kg loading dose followed by 5 mg/kg/day in two doses as maintenance. Thereafter, patients were divided into three groups based on the response to TPM therapy and seizure cessation time (full responder, partial responder, and nonresponder). Four patients received only thiopental, two received thiopental, and high-dose midazolam, one received thiopental, high-dose midazolam, and propofol, two received only propofol, one received propofol, and high-dose midazolam and four patients were on a high-dose midazolam infusion.

Results

The median time to seizure cessation was 5.5 h (range 2–48 h). Nine patients were full responders, three were partial responders, and two were nonresponders At follow-up, six patients were weaned successfully from thiopental, two patients from high-dose midazolam and three patients from propofol. Three patients developed mild metabolic acidosis during TPM theraphy.

Conclusions

Most of the patients responded to this treatment which was well tolerated. So we recommended its use for terminating refractory status epilepticus in children.
Literature
1.
go back to reference Abend NS, Dlugos DJ (2008) Treatment of refractory status epilepticus: literature review and proposed protocol. Pediatr Neurol 38:377–390PubMedCrossRef Abend NS, Dlugos DJ (2008) Treatment of refractory status epilepticus: literature review and proposed protocol. Pediatr Neurol 38:377–390PubMedCrossRef
2.
go back to reference Bensalem MK, Fakhoury TA (2003) Topiramate and status epilepticus: report of three cases. Epilepsy Behav 4:757–760PubMedCrossRef Bensalem MK, Fakhoury TA (2003) Topiramate and status epilepticus: report of three cases. Epilepsy Behav 4:757–760PubMedCrossRef
4.
go back to reference Blumkin L, Lerman-Sagie T, Houri T, Gilad E, Nissenkorn A, Ginsberg M, Watemberg M (2005) Pediatric refractory partial status epilepticus responsive to topiramate. J Child Neurol 20:239–241PubMed Blumkin L, Lerman-Sagie T, Houri T, Gilad E, Nissenkorn A, Ginsberg M, Watemberg M (2005) Pediatric refractory partial status epilepticus responsive to topiramate. J Child Neurol 20:239–241PubMed
5.
go back to reference Doose DR, Brodie MJ, Wilson EA et al (2003) Topiramate and lamotrigine pharmacokinetics during repetitive monotherapy and combination therapy in epilepsy patients. Epilepsia 44:917–922PubMedCrossRef Doose DR, Brodie MJ, Wilson EA et al (2003) Topiramate and lamotrigine pharmacokinetics during repetitive monotherapy and combination therapy in epilepsy patients. Epilepsia 44:917–922PubMedCrossRef
6.
go back to reference Doose DR, Walker SA, Gisclon LG, Nayak RK (1996) Single-dose pharmokinetics and effect of food on the bioavailability of topiramate, a novel antiepileptic drug. J Clin Pharmacol 36:884–891PubMed Doose DR, Walker SA, Gisclon LG, Nayak RK (1996) Single-dose pharmokinetics and effect of food on the bioavailability of topiramate, a novel antiepileptic drug. J Clin Pharmacol 36:884–891PubMed
7.
go back to reference Doose DR, Walker SA, Pledger G (1995) Evaluation of phenobarbital and primidone/phenobarbital plasma concentrations during administration of add-on topiramate theraphy in five multicenter, double-blind, placebo-controlled in ourpatients with partial seizures. Epilepsia 36(suppl 3):158 Doose DR, Walker SA, Pledger G (1995) Evaluation of phenobarbital and primidone/phenobarbital plasma concentrations during administration of add-on topiramate theraphy in five multicenter, double-blind, placebo-controlled in ourpatients with partial seizures. Epilepsia 36(suppl 3):158
8.
go back to reference Faught E, Wilder BJ, Ramsay RE, ReifeRA KLD, Pledger GW, Karim RM (1996) Topiramate placebo-controlled dose-ranging trial in refractory partial epilepsy using 200-, 400- and, 600-mg daily dosages. Topiramate YD Study Group Neurology 46:1684–1690 Faught E, Wilder BJ, Ramsay RE, ReifeRA KLD, Pledger GW, Karim RM (1996) Topiramate placebo-controlled dose-ranging trial in refractory partial epilepsy using 200-, 400- and, 600-mg daily dosages. Topiramate YD Study Group Neurology 46:1684–1690
9.
go back to reference Gallentine WB, Hunnicut AS, Husain AM (2009) Levatiracetam in children with refractory status epilepticus. Epilepsy Behav 14:215–218PubMedCrossRef Gallentine WB, Hunnicut AS, Husain AM (2009) Levatiracetam in children with refractory status epilepticus. Epilepsy Behav 14:215–218PubMedCrossRef
10.
go back to reference Glauser TA (2008) Topiramate. In: Pellock JM, Bourgeois BF, Dodson WE (eds) Pediatric epilepsy diagnosis and therapy, 3rd edn. Demos Medical Publishing, New York, pp 671–683 Glauser TA (2008) Topiramate. In: Pellock JM, Bourgeois BF, Dodson WE (eds) Pediatric epilepsy diagnosis and therapy, 3rd edn. Demos Medical Publishing, New York, pp 671–683
11.
go back to reference Holtkamp M (2007) The anaesthetic and intensive care of status epilepticus. Curr Opin Neurol 20:188–193PubMedCrossRef Holtkamp M (2007) The anaesthetic and intensive care of status epilepticus. Curr Opin Neurol 20:188–193PubMedCrossRef
12.
go back to reference Kahriman M, Minecan D, Kutluay E, Selwa L, Beydoun A (2003) Efficiacy of topiramate in children with refractory status epilepticus. Epilepsia 44:1353–1356PubMedCrossRef Kahriman M, Minecan D, Kutluay E, Selwa L, Beydoun A (2003) Efficiacy of topiramate in children with refractory status epilepticus. Epilepsia 44:1353–1356PubMedCrossRef
13.
go back to reference Kalvainen R, Eriksson K, Parvainen I (2005) Refractory generalized status epilepticus: a guide to treatment. CNS Drug 19:759–768CrossRef Kalvainen R, Eriksson K, Parvainen I (2005) Refractory generalized status epilepticus: a guide to treatment. CNS Drug 19:759–768CrossRef
14.
go back to reference Mayer SA, Claassen J, Lokin J, Mendelsohn F, Dennis LJ, Fitzsimmons BF (2002) Refractory status epilepticus: frequency, risk factors, and impact on outcome. Arch Neurol 59:205–210PubMedCrossRef Mayer SA, Claassen J, Lokin J, Mendelsohn F, Dennis LJ, Fitzsimmons BF (2002) Refractory status epilepticus: frequency, risk factors, and impact on outcome. Arch Neurol 59:205–210PubMedCrossRef
15.
go back to reference Nayak RK, Gisclon LG, Curtin CA (1994) Estimation of the absolute bioavailability of topiramate in humans without intravenous data. J Clin Pharmacol 34:1029 Nayak RK, Gisclon LG, Curtin CA (1994) Estimation of the absolute bioavailability of topiramate in humans without intravenous data. J Clin Pharmacol 34:1029
16.
go back to reference Niebauer M, Gruenthal M (1999) Topiramate reduces neuronal injury after experimental status epilepticus. Brain Res 837:263–269PubMedCrossRef Niebauer M, Gruenthal M (1999) Topiramate reduces neuronal injury after experimental status epilepticus. Brain Res 837:263–269PubMedCrossRef
17.
go back to reference Pellock JM (1999) Use of midazolam for refractory status epilepticus in pediatric patients. J Child Neurol 20:259–264 Pellock JM (1999) Use of midazolam for refractory status epilepticus in pediatric patients. J Child Neurol 20:259–264
18.
go back to reference Perry MS, Holt PJ, Sladky JT (2006) Topiramate loading for status epilepticus in children. Epilepsia 47:1070–1071PubMedCrossRef Perry MS, Holt PJ, Sladky JT (2006) Topiramate loading for status epilepticus in children. Epilepsia 47:1070–1071PubMedCrossRef
19.
go back to reference Privitera M, Fincham R, Penry J, Reife R, Kramer L, Pledger G, Karim R (1996) Topiramate placebo-controlled dose-ranging trial in refractory partial epilepsy using 600-,800-and, 1000-mg daily dosages. Topiramate YE Study Group Neurology 46:1678–1683 Privitera M, Fincham R, Penry J, Reife R, Kramer L, Pledger G, Karim R (1996) Topiramate placebo-controlled dose-ranging trial in refractory partial epilepsy using 600-,800-and, 1000-mg daily dosages. Topiramate YE Study Group Neurology 46:1678–1683
20.
go back to reference Sachdeo RC, Sachdeo SK, Walker SA, Kramer LD, Nayak RK, Doose DR (1996) Steady-state pharmacokinetics of topiramate and carbamazepine in patients with epilepsy during monotherapy and concomitant therapy. Epilepsia 37:774–780PubMedCrossRef Sachdeo RC, Sachdeo SK, Walker SA, Kramer LD, Nayak RK, Doose DR (1996) Steady-state pharmacokinetics of topiramate and carbamazepine in patients with epilepsy during monotherapy and concomitant therapy. Epilepsia 37:774–780PubMedCrossRef
21.
go back to reference Sahin M, Menache CC, Holmes GL (2001) Outcome of severe refractory status epilepticus in children. Epilepsia 42:1411–1467 Sahin M, Menache CC, Holmes GL (2001) Outcome of severe refractory status epilepticus in children. Epilepsia 42:1411–1467
22.
go back to reference Takeoka M, Holmes GL, Thiele E, Bourgeois BF, Helmers SL, Duffy FH, Riviello JJ (2001) Topiramate and metabolic acidosis in pediatric epilepsy. Epilepsia 42:387–392PubMedCrossRef Takeoka M, Holmes GL, Thiele E, Bourgeois BF, Helmers SL, Duffy FH, Riviello JJ (2001) Topiramate and metabolic acidosis in pediatric epilepsy. Epilepsia 42:387–392PubMedCrossRef
23.
go back to reference Towne AR, Garnett LK, Waterhouse EJ, Morton LD, DeLorenzo RJ (2003) The use of topiramate in refractory status epilepticus. Neurology 60:332–334PubMed Towne AR, Garnett LK, Waterhouse EJ, Morton LD, DeLorenzo RJ (2003) The use of topiramate in refractory status epilepticus. Neurology 60:332–334PubMed
24.
go back to reference Waugh J, Goa KL (2003) Topiramate: as monotheraphy in newly diagnosed epilepsy. CNS Drugs 17:985–992PubMedCrossRef Waugh J, Goa KL (2003) Topiramate: as monotheraphy in newly diagnosed epilepsy. CNS Drugs 17:985–992PubMedCrossRef
Metadata
Title
Treatment of pediatric refractory status epilepticus with topiramate
Authors
Başak Nur Akyıldız
Sefer Kumandaş
Publication date
01-09-2011
Publisher
Springer-Verlag
Published in
Child's Nervous System / Issue 9/2011
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-011-1432-y

Other articles of this Issue 9/2011

Child's Nervous System 9/2011 Go to the issue