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  1. Article ; Online: Early Treatment with Vigabatrin Does Not Decrease Focal Seizures or Improve Cognition in Tuberous Sclerosis Complex: The PREVeNT Trial.

    Bebin, Elizabeth Martina / Peters, Jurriaan M / Porter, Brenda E / McPherson, Tarrant O / O'Kelley, Sarah / Sahin, Mustafa / Taub, Katherine S / Rajaraman, Rajsekar / Randle, Stephanie C / McClintock, William M / Koenig, Mary Kay / Frost, Mike D / Northrup, Hope A / Werner, Klaus / Nolan, Danielle A / Wong, Michael / Krefting, Jessica L / Biasini, Fred / Peri, Kalyani /
    Cutter, Gary / Krueger, Darcy A

    Annals of neurology

    2023  

    Abstract: Objective: This study was undertaken to test the hypothesis that early vigabatrin treatment in tuberous sclerosis complex (TSC) infants improves neurocognitive outcome at 24 months of age.: Methods: A phase IIb multicenter randomized double-blind ... ...

    Abstract Objective: This study was undertaken to test the hypothesis that early vigabatrin treatment in tuberous sclerosis complex (TSC) infants improves neurocognitive outcome at 24 months of age.
    Methods: A phase IIb multicenter randomized double-blind placebo-controlled trial was conducted of vigabatrin at first epileptiform electroencephalogram (EEG) versus vigabatrin at seizure onset in infants with TSC. Primary outcome was Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III) cognitive assessment score at 24 months. Secondary outcomes were prevalence of drug-resistant epilepsy, additional developmental outcomes, and safety of vigabatrin.
    Results: Of 84 infants enrolled, 12 were screen failures, 4 went straight to open label vigabatrin, and 12 were not randomized (normal EEG throughout). Fifty-six were randomized to early vigabatrin (n = 29) or placebo (n = 27). Nineteen of 27 in the placebo arm transitioned to open label vigabatrin, with a median delay of 44 days after randomization. Bayley-III cognitive composite scores at 24 months were similar for participants randomized to vigabatrin or placebo. Additionally, no significant differences were found between groups in overall epilepsy incidence and drug-resistant epilepsy at 24 months, time to first seizure after randomization, and secondary developmental outcomes. Incidence of infantile spasms was lower and time to spasms after randomization was later in the vigabatrin group. Adverse events were similar across groups.
    Interpretation: Preventative treatment with vigabatrin based on EEG epileptiform activity prior to seizure onset does not improve neurocognitive outcome at 24 months in TSC children, nor does it delay onset or lower the incidence of focal seizures and drug-resistant epilepsy at 24 months. Preventative vigabatrin was associated with later time to onset and lower incidence of infantile spasms. ANN NEUROL 2023.
    Language English
    Publishing date 2023-08-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80362-5
    ISSN 1531-8249 ; 0364-5134
    ISSN (online) 1531-8249
    ISSN 0364-5134
    DOI 10.1002/ana.26778
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Pilot Study of Neurodevelopmental Impact of Early Epilepsy Surgery in Tuberous Sclerosis Complex.

    Grayson, Leslie E / Peters, Jurriaan M / McPherson, Tarrant / Krueger, Darcy A / Sahin, Mustafa / Wu, Joyce Y / Northrup, Hope A / Porter, Brenda / Cutter, Gary R / O'Kelley, Sarah E / Krefting, Jessica / Stone, Scellig S / Madsen, Joseph R / Fallah, Aria / Blount, Jeffrey P / Weiner, Howard L / Bebin, E Martina

    Pediatric neurology

    2020  Volume 109, Page(s) 39–46

    Abstract: Background: To determine if early epilepsy surgery mitigates detrimental effects of refractory epilepsy on development, we investigated surgical and neurodevelopmental outcomes in children with tuberous sclerosis complex who underwent surgery before age ...

    Abstract Background: To determine if early epilepsy surgery mitigates detrimental effects of refractory epilepsy on development, we investigated surgical and neurodevelopmental outcomes in children with tuberous sclerosis complex who underwent surgery before age two years.
    Methods: Prospective multicenter observational study of 160 children with tuberous sclerosis complex. Surgical outcome was determined for the seizure type targeted by surgery. We obtained Vineland Adaptive Behavior Scales, Second Edition (Vineland-II); Mullen Scales of Early Learning; and Preschool Language Scales, Fifth Edition, at age three, six, nine, 12, 18, 24, and 36 months. Surgical cases were compared with children without seizures, with controlled seizures, and with medically refractory seizures.
    Results: Nineteen children underwent surgery (median age 17 months, range 3.7 to 21.3), and mean follow-up was 22.8 months (range 12 to 48). Surgical outcomes were favorable in 12 (63%, Engel I-II) and poor in seven (37%, Engel III-IV). Nine (47%) had new or ongoing seizures distinct from those surgically targeted. All children with seizures demonstrated longitudinal decline or attenuated gains in neurodevelopment, the surgical group scoring the lowest. Favorable surgical outcome was associated with increased Mullen Scales of Early Learning receptive and expressive language subscores compared with the medically refractory seizure group. A nonsignificant but consistent pattern of improvement with surgery was seen in all tested domains.
    Conclusions: These pilot data show neurodevelopmental gains in some domains following epilepsy surgery. A properly powered, prospective multicenter observational study of early epilepsy surgery is needed, using both surgical and developmental outcome metrics.
    MeSH term(s) Child, Preschool ; Drug Resistant Epilepsy/etiology ; Drug Resistant Epilepsy/surgery ; Female ; Follow-Up Studies ; Humans ; Infant ; Male ; Neurodevelopmental Disorders/etiology ; Neurodevelopmental Disorders/surgery ; Outcome Assessment, Health Care ; Pilot Projects ; Tuberous Sclerosis/complications
    Language English
    Publishing date 2020-04-14
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Observational Study ; Research Support, N.I.H., Extramural
    ZDB-ID 639164-3
    ISSN 1873-5150 ; 0887-8994
    ISSN (online) 1873-5150
    ISSN 0887-8994
    DOI 10.1016/j.pediatrneurol.2020.04.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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