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Protocol for multicentre comparison of interictal high-frequency oscillations as a predictor of seizure freedom

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F22%3A00077781" target="_blank" >RIV/00159816:_____/22:00077781 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://academic.oup.com/braincomms/article/4/3/fcac151/6604800?login=true" target="_blank" >https://academic.oup.com/braincomms/article/4/3/fcac151/6604800?login=true</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/braincomms/fcac151" target="_blank" >10.1093/braincomms/fcac151</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Protocol for multicentre comparison of interictal high-frequency oscillations as a predictor of seizure freedom

  • Popis výsledku v původním jazyce

    In drug-resistant focal epilepsy, interictal high-frequency oscillations (HFOs) recorded from intracranial EEG (iEEG) may provide clinical information for delineating epileptogenic brain tissue. The iEEG electrode contacts that contain HFO are hypothesized to delineate the epileptogenic zone; their resection should then lead to postsurgical seizure freedom. We test whether our prospective definition of clinically relevant HFO is in agreement with postsurgical seizure outcome. The algorithm is fully automated and is equally applied to all data sets. The aim is to assess the reliability of the proposed detector and analysis approach. We use an automated data-independent prospective definition of clinically relevant HFO that has been validated in data from two independent epilepsy centres. In this study, we combine retrospectively collected data sets from nine independent epilepsy centres. The analysis is blinded to clinical outcome. We use iEEG recordings during NREM sleep with a minimum of 12 epochs of 5 min of NREM sleep. We automatically detect HFO in the ripple (80-250 Hz) and in the fast ripple (250-500 Hz) band. There is no manual rejection of events in this fully automated algorithm. The type of HFO that we consider clinically relevant is defined as the simultaneous occurrence of a fast ripple and a ripple. We calculate the temporal consistency of each patient&apos;s HFO rates over several data epochs within and between nights. Patients with temporal consistency &lt;50% are excluded from further analysis. We determine whether all electrode contacts with high HFO rate are included in the resection volume and whether seizure freedom (ILAE 1) was achieved at &gt;= 2 years follow-up. Applying a previously validated algorithm to a large cohort from several independent epilepsy centres may advance the clinical relevance and the generalizability of HFO analysis as essential next step for use of HFO in clinical practice. High-frequency oscillations (HFOs) have long been discussed as biomarkers for epileptogenic tissue. Dimakopoulos et al. propose a prospective multicentre study to validate whether HFOs in intracranial EEG recorded during sleep may serve to predict the seizure outcome after epilepsy surgery.

  • Název v anglickém jazyce

    Protocol for multicentre comparison of interictal high-frequency oscillations as a predictor of seizure freedom

  • Popis výsledku anglicky

    In drug-resistant focal epilepsy, interictal high-frequency oscillations (HFOs) recorded from intracranial EEG (iEEG) may provide clinical information for delineating epileptogenic brain tissue. The iEEG electrode contacts that contain HFO are hypothesized to delineate the epileptogenic zone; their resection should then lead to postsurgical seizure freedom. We test whether our prospective definition of clinically relevant HFO is in agreement with postsurgical seizure outcome. The algorithm is fully automated and is equally applied to all data sets. The aim is to assess the reliability of the proposed detector and analysis approach. We use an automated data-independent prospective definition of clinically relevant HFO that has been validated in data from two independent epilepsy centres. In this study, we combine retrospectively collected data sets from nine independent epilepsy centres. The analysis is blinded to clinical outcome. We use iEEG recordings during NREM sleep with a minimum of 12 epochs of 5 min of NREM sleep. We automatically detect HFO in the ripple (80-250 Hz) and in the fast ripple (250-500 Hz) band. There is no manual rejection of events in this fully automated algorithm. The type of HFO that we consider clinically relevant is defined as the simultaneous occurrence of a fast ripple and a ripple. We calculate the temporal consistency of each patient&apos;s HFO rates over several data epochs within and between nights. Patients with temporal consistency &lt;50% are excluded from further analysis. We determine whether all electrode contacts with high HFO rate are included in the resection volume and whether seizure freedom (ILAE 1) was achieved at &gt;= 2 years follow-up. Applying a previously validated algorithm to a large cohort from several independent epilepsy centres may advance the clinical relevance and the generalizability of HFO analysis as essential next step for use of HFO in clinical practice. High-frequency oscillations (HFOs) have long been discussed as biomarkers for epileptogenic tissue. Dimakopoulos et al. propose a prospective multicentre study to validate whether HFOs in intracranial EEG recorded during sleep may serve to predict the seizure outcome after epilepsy surgery.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30210 - Clinical neurology

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2022

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    BRAIN COMMUNICATIONS

  • ISSN

    2632-1297

  • e-ISSN

    2632-1297

  • Svazek periodika

    4

  • Číslo periodika v rámci svazku

    3

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    8

  • Strana od-do

    nestrankovano

  • Kód UT WoS článku

    000816825400001

  • EID výsledku v databázi Scopus