Počet záznamů: 1  

Prediction of Vagal Nerve Stimulation Efficacy in Drug-Resistant Epilepsy (PRECISE): Prospective Study for Pre-implantation Prediction/Study Design

  1. 1.
    SYSNO ASEP0564514
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevPrediction of Vagal Nerve Stimulation Efficacy in Drug-Resistant Epilepsy (PRECISE): Prospective Study for Pre-implantation Prediction/Study Design
    Tvůrce(i) Doležalová, I. (CZ)
    Koriťáková, E. (CZ)
    Součková, L. (CZ)
    Chrastina, J. (CZ)
    Chládek, Jan (UPT-D) RID, ORCID, SAI
    Štěpánová, R. (CZ)
    Brázdil, M. (CZ)
    Celkový počet autorů7
    Číslo článku839163
    Zdroj.dok.Frontiers in Neurology. - : Frontiers Media - ISSN 1664-2295
    Roč. 13, 21 March (2022)
    Poč.str.9 s.
    Forma vydáníOnline - E
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovadrug-resistant epilepsy ; vagal nerve stimulation ; efficacy prediction ; statistical model ; study design
    Vědní obor RIVFH - Neurologie, neurochirurgie, neurovědy
    Obor OECDNeurosciences (including psychophysiology
    CEPNV19-04-00343 GA MZd - Ministerstvo zdravotnictví
    Výzkumná infrastrukturaCZECRIN III - 90128 - Masarykova univerzita
    Způsob publikováníOpen access
    Institucionální podporaUPT-D - RVO:68081731
    UT WOS000860449700001
    EID SCOPUS85128055608
    DOI10.3389/fneur.2022.839163
    AnotaceBackground: Vagal nerve stimulation (VNS) can be indicated in patients with drug-resistant epilepsy, who are not eligible for resective epilepsy surgery. In VNS therapy, the responder rate (i.e., percentage of subjects experiencing ≥50% seizure reduction) is ~50%. At the moment, there is no widely-accepted possibility to predict VNS efficacy in a particular patient based on pre-implantation data, which can lead to unnecessary surgery and improper allocation of financial resources. The principal aim of PRediction of vagal nerve stimulation EfficaCy In drug-reSistant Epilepsy (PRECISE) study is to verify the predictability of VNS efficacy by analysis of pre-implantation routine electroencephalogram (EEG). Methods: PRECISE is designed as a prospective multicentric study in which patients indicated to VNS therapy will be recruited. Patients will be classified as predicted responders vs. predicted non-responders using pre-implantation EEG analyses. After the first and second year of the study, the real-life outcome (responder vs. non-responder) will be determined. The real-life outcome and predicted outcome will be compared in terms of accuracy, specificity, and sensitivity. In the meantime, the patients will be managed according to the best clinical practice to obtain the best therapeutic response. The primary endpoint will be the accuracy of the statistical model for prediction of response to VNS therapy in terms of responders and non-responders. The secondary endpoint will be the quantification of differences in EEG power spectra (Relative Mean Power, %) between real-life responders and real-life non-responders to VNS therapy in drug-resistant epilepsy and the sensitivity and specificity of the model. Discussion: PRECISE relies on the results of our previous work, through which we developed a statistical classifier for VNS response (responders vs. non-responders) based on differences in EEG power spectra dynamics (Pre-X-Stim).
    PracovištěÚstav přístrojové techniky
    KontaktMartina Šillerová, sillerova@ISIBrno.Cz, Tel.: 541 514 178
    Rok sběru2023
    Elektronická adresahttps://www.frontiersin.org/articles/10.3389/fneur.2022.839163/full
Počet záznamů: 1  

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