Page last updated: 2024-10-28

lidocaine and Epilepsies, Myoclonic

lidocaine has been researched along with Epilepsies, Myoclonic in 5 studies

Lidocaine: A local anesthetic and cardiac depressant used as an antiarrhythmia agent. Its actions are more intense and its effects more prolonged than those of PROCAINE but its duration of action is shorter than that of BUPIVACAINE or PRILOCAINE.
lidocaine : The monocarboxylic acid amide resulting from the formal condensation of N,N-diethylglycine with 2,6-dimethylaniline.

Epilepsies, Myoclonic: A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic.

Research Excerpts

ExcerptRelevanceReference
"The treatment with lidocaine followed by mexiletine was useful for controlling clusters of intractable seizures."5.30[A successful treatment with intravenous lidocaine followed by oral mexiletine in a patient with Lennox-Gastaut syndrome]. ( Miyamoto, A; Oki, J; Takahashi, S, 1999)
"We describe a two-year-old boy with Dravet syndrome, a severe genetic epilepsy, who developed a generalized tonic-clonic seizure immediately following an intravenous bolus of lidocaine given for propofol pain amelioration during induction of anesthesia for emergency gastroscopy."4.12Anesthetic considerations in Dravet syndrome. ( Corlette, S; Davidson, A; Howell, KB; Macdonald-Laurs, E, 2022)
"NaV1."1.42Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome. ( Catterall, WA; Jones, CJ; Rubinstein, M; Scheuer, T; Westenbroek, RE; Yu, FH, 2015)
"The treatment with lidocaine followed by mexiletine was useful for controlling clusters of intractable seizures."1.30[A successful treatment with intravenous lidocaine followed by oral mexiletine in a patient with Lennox-Gastaut syndrome]. ( Miyamoto, A; Oki, J; Takahashi, S, 1999)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Macdonald-Laurs, E1
Corlette, S1
Davidson, A1
Howell, KB1
Rubinstein, M1
Westenbroek, RE1
Yu, FH1
Jones, CJ1
Scheuer, T1
Catterall, WA1
Rothner, AD1
Erenberg, G1
Kanemura, H1
Aihara, M1
Sata, Y1
Hatakeyama, K1
Hinohara, Y1
Kamiya, Y1
Shimoda, C1
Nakazawa, S1
Miyamoto, A1
Takahashi, S1
Oki, J1

Other Studies

5 other studies available for lidocaine and Epilepsies, Myoclonic

ArticleYear
Anesthetic considerations in Dravet syndrome.
    Paediatric anaesthesia, 2022, Volume: 32, Issue:10

    Topics: Anesthetics; Anticonvulsants; Child, Preschool; Epilepsies, Myoclonic; Epilepsy; Epileptic Syndromes

2022
Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
    Neurobiology of disease, 2015, Volume: 73

    Topics: Action Potentials; Animals; Animals, Newborn; Biophysical Phenomena; Conditioning, Psychological; Di

2015
Status epilepticus.
    Pediatric clinics of North America, 1980, Volume: 27, Issue:3

    Topics: Anesthesia, General; Child; Child, Preschool; Diazepam; Epilepsies, Myoclonic; Epilepsies, Partial;

1980
[A successful treatment with a continuous intravenous lidocaine for a cluster of minor seizures in a patient with Doose syndrome].
    No to hattatsu = Brain and development, 1996, Volume: 28, Issue:4

    Topics: Child; Epilepsies, Myoclonic; Female; Humans; Infusions, Intravenous; Lidocaine

1996
[A successful treatment with intravenous lidocaine followed by oral mexiletine in a patient with Lennox-Gastaut syndrome].
    No to hattatsu = Brain and development, 1999, Volume: 31, Issue:5

    Topics: Administration, Oral; Adolescent; Epilepsies, Myoclonic; Epilepsy, Absence; Epilepsy, Generalized; H

1999