1993
DOI: 10.1001/archneur.1993.00540010020012
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Long-term Antiepileptic Efficacy of Vigabatrin in Drug-Refractory Epilepsy in Mentally Retarded Patients

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Cited by 35 publications
(15 citation statements)
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“…Another study in adult patients with learning disability and resistant epilepsy showed responder rates of 50% for gabapentin and 48.6% for LTG [17]. Vigabatrin (VGB) used in patients with refractory epilepsy and mental retardation showed responder rates of 42% at three months and 33% at one year [18]. In the present study, TPM add-on therapy showed equal or better results.…”
Section: Discussionsupporting
confidence: 47%
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“…Another study in adult patients with learning disability and resistant epilepsy showed responder rates of 50% for gabapentin and 48.6% for LTG [17]. Vigabatrin (VGB) used in patients with refractory epilepsy and mental retardation showed responder rates of 42% at three months and 33% at one year [18]. In the present study, TPM add-on therapy showed equal or better results.…”
Section: Discussionsupporting
confidence: 47%
“…Ages at TPM add-on therapy ranged from five months to fourteen years. CNS anomalies included proliferation disorders (n=10, patients 1-10), migration or organization disorders (n=10, patients [11][12][13][14][15][16][17][18][19][20], and neurocutaneous syndromes (n=2, patients [21][22]. Types of epilepsies at TPM add-on therapy were symptomatic partial epilepsies (SPE) (n=11), infantile spasms (IS) (n=7), and Lennox-Gastaut syndrome (LGS) (n=4).…”
Section: Resultsmentioning
confidence: 99%
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“…Improved seizure control also has been claimed with LTG in observational studies (12)(13)(14). VGB reduced seizures by Ն50% in 36 patients with learning disability with a gradual reduction to 22% of patients after 5 years' follow-up (15). This drug is more often associated with behavioural problems than are LTG and GBP in this population (16).…”
Section: Discussionmentioning
confidence: 66%
“…247 Psychosis was the reason for withdrawal in a follow-up study of patients described as mentally retarded, which also reported that psychiatric AEs often appeared during the second year of treatment (up to 3 g/day VGB). 248 Psychosis was the reason for withdrawal of one patient after 1 year in an open-label extension study in which two more patients experienced dose-related psychotic symptoms. The dose range reached 5 g/day.…”
mentioning
confidence: 99%