Refractory idiopathic absence status epilepticus: A probable paradoxical effect of phenytoin and carbamazepine

被引:56
作者
Osorio, I
Reed, RC
Peltzer, JN
机构
[1] Univ Kansas, Med Ctr, Comprehens Epilepsy Ctr, Kansas City, KS 66160 USA
[2] Case Western Reserve Univ, Dept Neurol, Cleveland, OH 44106 USA
关键词
idiopathic generalized epilepsies; absence status epilepticus; refractoriness; paradoxical effects; phenytoin; carbamazepine;
D O I
10.1111/j.1528-1157.2000.tb00258.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: To compare the frequency of seizures and status epilepticus and their response to first-line drugs in patients with idiopathic generalized epilepsies receiving carbamazepine or phenytoin to those receiving other drugs or no treatment. Methods: We performed a retrospective chart review of all cases of idiopathic generalized epilepsies treated by the authors between 1985 and 1994. We compared seizure frequency and mean intravenous benzodiazepine dose required to control absence status epilepticus, intraindividually in subjects on carbamazepine or phenytoin before and after discontinuation of these compounds, and interindividually to subjects without treatment or receiving other drugs. Results: Bouts of absence or tonic-clonic status epilepticus and seizures in subjects treated with phenytoin or carbamazepine at therapeutic concentrations were considerably more frequent and proved intractable to treatment with valproic acid or benzodiazepines, compared with a cohort of subjects also with idiopathic generalized epilepsies, but naive to, or receiving subtherapeutic or therapeutic doses of other agents. Conclusions: Our observations strongly suggest that therapeutic concentrations of phenytoin and carbamazepine exacerbate idiopathic generalized epilepsies. Subjects in whom absence is one of the seizure types seem at a particularly high risk for responding paradoxically. These findings underscore the value of accurate classification of seizures and particularly the syndromic approach to diagnosis and point to the potential for iatrogenic complications with indiscriminate use of antiseizure drugs.
引用
收藏
页码:887 / 894
页数:8
相关论文
共 60 条
[1]   ABSENCE STATUS - REAPPRAISAL FOLLOWING REVIEW OF 38 PATIENTS [J].
ANDERMANN, F ;
ROBB, JP .
EPILEPSIA, 1972, 13 (01) :177-+
[2]  
[Anonymous], 1994, EPILEPTIC SEIZURES S
[3]   Seizure-inducing effects of antiepileptic drugs: A review [J].
Bauer, J .
ACTA NEUROLOGICA SCANDINAVICA, 1996, 94 (06) :367-377
[4]   Double-blind, placebo-controlled, crossover study of lamotrigine in treatment-resistant generalised epilepsy [J].
Beran, RG ;
Berkovic, SF ;
Dunagan, FM ;
Vajda, FJE ;
Danta, G ;
Black, AB ;
Mackenzie, R .
EPILEPSIA, 1998, 39 (12) :1329-1333
[5]   BENZODIAZEPINES IN TREATMENT OF EPILEPSY - REVIEW [J].
BROWNE, TR ;
PENRY, JK .
EPILEPSIA, 1973, 14 (03) :277-310
[6]  
Buchanan N, 1996, SEIZURE, V5, P149
[7]   PROLONGED ABSENCE STATUS EPILEPTICUS ASSOCIATED WITH CARBAMAZEPINE THERAPY, INCREASED INTRACRANIAL-PRESSURE, AND TRANSIENT MRI ABNORMALITIES [J].
CALLAHAN, DJ ;
NOETZEL, MJ .
NEUROLOGY, 1992, 42 (11) :2198-2201
[8]  
CASCINO G, 1993, EPILEPSIA S1, V34, P21
[9]   Antiepileptic drug cellular mechanisms of action: Where does lamotrigine fit in? [J].
Coulter, DA .
JOURNAL OF CHILD NEUROLOGY, 1997, 12 :S2-S9
[10]   DIFFERENTIAL-EFFECTS OF PETIT-MAL ANTICONVULSANTS AND CONVULSANTS ON THALAMIC NEURONS - CALCIUM CURRENT REDUCTION [J].
COULTER, DA ;
HUGUENARD, JR ;
PRINCE, DA .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 100 (04) :800-806