Method for prediction of clinical response to VNS therapy in epileptic patients
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F20%3A00117541" target="_blank" >RIV/00216224:14110/20:00117541 - isvavai.cz</a>
Výsledek na webu
<a href="https://worldwide.espacenet.com/patent/search/family/059558210/publication/EP3437692B1?q=EP3437692B1" target="_blank" >https://worldwide.espacenet.com/patent/search/family/059558210/publication/EP3437692B1?q=EP3437692B1</a>
DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Method for prediction of clinical response to VNS therapy in epileptic patients
Popis výsledku v původním jazyce
The present invention provides a method for determining of clinical response of a patient suffering from epilepsy to chronic vagal nerve stimulation (VNS) therapy, which comprises the steps of: - obtaining theta, alpha, beta and gamma frequency bands for at least one, preferably at least 10 scalp electrodes from scalp EEG data obtained from the patient using an EEG recording protocol, said EEG data comprising at least one rest interval, preferably at the beginning of the EEG data, at least one open eyes/close eyes interval, at least one photic stimulation interval, at least one hyperventilation interval, and optionally at least one additional open eyes/close eyes interval and optionally at least one rest interval having the duration of at least 30 s at the end of the EEG data, wherein one interval is selected as a baseline interval, - obtaining absolute mean powers as mean values of passband power envelope inside at least one discriminative interval and inside the baseline interval, and obtaining the relative mean power of the at least one discriminative interval as the ratio of the absolute mean power of said discriminative interval relative to the absolute mean power of the baseline interval, - determining from the relative mean powers of the at least one discriminative interval for at least one discriminative electrode whether the patient is a responder or a non-responder to vagal nerve stimulation therapy based on a responder pattern or a non-responder pattern, wherein the responder and non-responder patterns, and optionally the discriminative electrodes and/or the discriminative intervals, are determined by statistical analysis of EEG data recorded using the said EEG recording protocol for a group of known responders and non-responders. The method of the invention is the first method of prediction of VNS therapeutic outcome using pre-VNS EEG data.
Název v anglickém jazyce
Method for prediction of clinical response to VNS therapy in epileptic patients
Popis výsledku anglicky
The present invention provides a method for determining of clinical response of a patient suffering from epilepsy to chronic vagal nerve stimulation (VNS) therapy, which comprises the steps of: - obtaining theta, alpha, beta and gamma frequency bands for at least one, preferably at least 10 scalp electrodes from scalp EEG data obtained from the patient using an EEG recording protocol, said EEG data comprising at least one rest interval, preferably at the beginning of the EEG data, at least one open eyes/close eyes interval, at least one photic stimulation interval, at least one hyperventilation interval, and optionally at least one additional open eyes/close eyes interval and optionally at least one rest interval having the duration of at least 30 s at the end of the EEG data, wherein one interval is selected as a baseline interval, - obtaining absolute mean powers as mean values of passband power envelope inside at least one discriminative interval and inside the baseline interval, and obtaining the relative mean power of the at least one discriminative interval as the ratio of the absolute mean power of said discriminative interval relative to the absolute mean power of the baseline interval, - determining from the relative mean powers of the at least one discriminative interval for at least one discriminative electrode whether the patient is a responder or a non-responder to vagal nerve stimulation therapy based on a responder pattern or a non-responder pattern, wherein the responder and non-responder patterns, and optionally the discriminative electrodes and/or the discriminative intervals, are determined by statistical analysis of EEG data recorded using the said EEG recording protocol for a group of known responders and non-responders. The method of the invention is the first method of prediction of VNS therapeutic outcome using pre-VNS EEG data.
Klasifikace
Druh
P - Patent
CEP obor
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OECD FORD obor
30210 - Clinical neurology
Návaznosti výsledku
Projekt
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Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2020
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Číslo patentu nebo vzoru
EP3437692B1
Vydavatel
EPO_1 -
Název vydavatele
European Patent Office
Místo vydání
Munich, The Hague, Berlin, Vienna, Brussels
Stát vydání
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Datum přijetí
26. 8. 2020
Název vlastníka
Masarykova univerzita
Způsob využití
A - Výsledek využívá pouze poskytovatel
Druh možnosti využití
A - K využití výsledku jiným subjektem je vždy nutné nabytí licence