Literature DB >> 312731

Chronic cerebellar stimulation in the treatment of epilepsy.

L F Levy, W C Auchterlonie.   

Abstract

Six cases of intractable epilepsy who were subjected to chronic cerebellar stimulation are reported. They had all been treated with a wide range of anticonvulsant drugs without success. The ages varied between 17 and 55 years. Three were genetic-inherent, 2 were of unknown etiology, and 1 was symptomatic (infection? trauma?). Four had generalized major convulsions and 2 had a mixture of major and minor attacks, 1 with a strong temporal lobe component. Stimulation was commenced in all cases as soon as the patients had a postoperative seizure. Headache occurred in all cases and necessitated reduction in the strength of the stimulation to between 2 and 4 V in all cases except 1. Occipital nerve block temporarily relieved 1 patient, but posterior root section of C2-C3 and part of C4 did not prevent headaches in another case. Two patients were greatly improved and managed to hold employment whereas formerly they had been unemployed. One patient felt 50% improved but there was no reduction in his seizure frequency; another had a 50% reduction in seizures but felt no better. One patient was noted to be improved intellectually although her seizures were more frequent. The remaining patient was unchanged. One patient committed suicide and another drowned. One prosthesis became infected and had to be removed.

Entities:  

Mesh:

Year:  1979        PMID: 312731     DOI: 10.1111/j.1528-1157.1979.tb04800.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  14 in total

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5.  A double-blind trial of chronic cerebellar stimulation in twelve patients with severe epilepsy.

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8.  Novel applications of deep brain stimulation.

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Review 9.  The cerebellum and epilepsy.

Authors:  Martha L Streng; Esther Krook-Magnuson
Journal:  Epilepsy Behav       Date:  2020-02-05       Impact factor: 3.337

10.  Cerebellar Directed Optogenetic Intervention Inhibits Spontaneous Hippocampal Seizures in a Mouse Model of Temporal Lobe Epilepsy.

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