Literature DB >> 12609161

Presentation, evaluation, and treatment of nonconvulsive status epilepticus.

F W Drislane1.   

Abstract

Nonconvulsive status epilepticus (NCSE) is much more common than is generally appreciated. It is certainly underdiagnosed, but its presentation is protean. Diagnostic criteria and treatment are controversial. Absence status is characterized by confusion or diminished responsiveness, with occasional blinking or twitching, lasting hours to days, with generalized spike and slow wave discharges on the EEG. Complex partial status consists of prolonged or repetitive complex partial seizures (with a presumed focal onset) and produces an "epileptic twilight state" with fluctuating lack of responsiveness or confusion. There is a clear overlapping of syndromes. Other confused, stuporous, or comatose patients with rapid, rhythmic, epileptiform discharges on the EEG may have "electrographic" status and should be considered in the same diagnostic category. NCSE typically occurs following supposedly controlled convulsions or other seizures, but with persistent neurologic dysfunction despite apparently adequate treatment. Confusion in the elderly or among emergency room patients is also a typical setting. The diagnosis of NCSE usually involves an abnormal mental status with diminished responsiveness, a supportive EEG, and often a response to anticonvulsant medication. All patients have clinical neurologic deficits, but the EEG findings and response to seizure medication are variable and are more controversial criteria. The response to drugs can be delayed for up to days. Experimental models and pathologic studies showing neuronal damage from status epilepticus pertain primarily to generalized convulsive status. Most morbidity from NCSE appears due to the underlying illness rather than to the NCSE itself. Some cases of prolonged NCSE or those with concomitant systemic illness, focal lesions, or very rapid epileptiform discharges may suffer more long-lasting damage. Although clinical studies show little evidence of permanent neurologic injury, the prolonged memory dysfunction in several cases and the similarities to convulsive status suggest that NCSE should be treated expeditiously. The diagnosis is important to make because NCSE impairs the patient's health significantly, and it is often a treatable and completely reversible condition.

Entities:  

Year:  2000        PMID: 12609161     DOI: 10.1006/ebeh.2000.0100

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  29 in total

Review 1.  Development of the calcium plateau following status epilepticus: role of calcium in epileptogenesis.

Authors:  Nisha Nagarkatti; Laxmikant S Deshpande; Robert J DeLorenzo
Journal:  Expert Rev Neurother       Date:  2009-06       Impact factor: 4.618

2.  Endocannabinoids block status epilepticus in cultured hippocampal neurons.

Authors:  Laxmikant S Deshpande; Robert E Blair; Julie M Ziobro; Sompong Sombati; Billy R Martin; Robert J DeLorenzo
Journal:  Eur J Pharmacol       Date:  2006-11-22       Impact factor: 4.432

Review 3.  Recommendations on the use of EEG monitoring in critically ill patients: consensus statement from the neurointensive care section of the ESICM.

Authors:  Jan Claassen; Fabio S Taccone; Peter Horn; Martin Holtkamp; Nino Stocchetti; Mauro Oddo
Journal:  Intensive Care Med       Date:  2013-05-08       Impact factor: 17.440

4.  Nonconvulsive status epilepticus disguising as hepatic encephalopathy.

Authors:  Yong Min Jo; Sung Wook Lee; Sang Young Han; Yang Hyun Baek; Ji Hye Ahn; Won Jong Choi; Ji Young Lee; Sang Ho Kim; Byeol A Yoon
Journal:  World J Gastroenterol       Date:  2015-04-28       Impact factor: 5.742

Review 5.  Cellular mechanisms underlying acquired epilepsy: the calcium hypothesis of the induction and maintainance of epilepsy.

Authors:  Robert J Delorenzo; David A Sun; Laxmikant S Deshpande
Journal:  Pharmacol Ther       Date:  2004-12-09       Impact factor: 12.310

6.  Non-convulsive status epilepticus: usefulness of clinical features in selecting patients for urgent EEG.

Authors:  A M Husain; G J Horn; M P Jacobson
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-02       Impact factor: 10.154

7.  Time course and mechanism of hippocampal neuronal death in an in vitro model of status epilepticus: role of NMDA receptor activation and NMDA dependent calcium entry.

Authors:  Laxmikant S Deshpande; Jeffrey K Lou; Ali Mian; Robert E Blair; Sompong Sombati; Elisa Attkisson; Robert J DeLorenzo
Journal:  Eur J Pharmacol       Date:  2008-02-05       Impact factor: 4.432

8.  Development of pharmacoresistance to benzodiazepines but not cannabinoids in the hippocampal neuronal culture model of status epilepticus.

Authors:  Laxmikant S Deshpande; Robert E Blair; Nisha Nagarkatti; Sompong Sombati; Billy R Martin; Robert J DeLorenzo
Journal:  Exp Neurol       Date:  2007-01-09       Impact factor: 5.330

Review 9.  Electroencephalographic monitoring in the pediatric intensive care unit.

Authors:  Nicholas S Abend; Kevin E Chapman; William B Gallentine; Joshua Goldstein; Ann E Hyslop; Tobias Loddenkemper; Kendall B Nash; James J Riviello; Cecil D Hahn
Journal:  Curr Neurol Neurosci Rep       Date:  2013-03       Impact factor: 5.081

10.  Carisbamate prevents the development and expression of spontaneous recurrent epileptiform discharges and is neuroprotective in cultured hippocampal neurons.

Authors:  Laxmikant S Deshpande; Nisha Nagarkatti; Julie M Ziobro; Sompong Sombati; Robert J DeLorenzo
Journal:  Epilepsia       Date:  2008-05-20       Impact factor: 5.864

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