Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17939
Title: Refractory focal motor seizures controlled with intramuscular botulinum toxin.
Austin Authors: Lee, Wei-I;Carney, Patrick W ;Hughes, Andrew J ;Archer, John S 
Affiliation: Department of Neurology, Austin Health, Heidelberg, Victoria, Australia
Department of Neurology, Box Hill Hospital, Box Hill, Melbourne, Australia
The University of Melbourne, Australia
Issue Date: Jul-2017
Date: 2017-04-10
Publication information: Epilepsy research 2017; 133: 93-97
Abstract: Patients with recurrent focal motor seizures present a management dilemma, as anti-convulsants are often ineffective, and resective surgery poses a high risk of motor deficit. We describe three patients with recurrent focal motor seizures that remained refractory despite numerous anti-convulsant trials. All patients showed either hyperperfusion on Single-Photon Emission Computerised Tomography (SPECT) or hypermetabolism on Positron Emission Tomography (PET) in primary motor cortex during periods of sustained jerking, although EEG abnormalities were uncommon. After botulinum toxin (BoT) injection there was a rapid and dramatic reduction in seizure frequency in all patients despite minimal limb weakness. Seizure freedom persisted for 3-6 months following treatment in the injected area. Repeat BoT injections following seizure recurrence were again efficacious in one case. Combining data from our cases with those previously reported, it appears that BoT may be a useful therapeutic tool for recurrent focal motor seizures. We hypothesise that the toxin disrupts or down-regulates an epileptic circuit between motor cortex and muscle, in which volleys of information from muscle spindles have been perpetuating seizure discharges in the cortex.
URI: https://ahro.austin.org.au/austinjspui/handle/1/17939
DOI: 10.1016/j.eplepsyres.2017.04.009
Journal: Epilepsy research
PubMed URL: 28475998
Type: Journal Article
Subjects: Botox
EPC
Epilepsy network
Epilepsy partialis continua
Status
Appears in Collections:Journal articles

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