scholarly journals Drug Resistant Epilepsy and the hypothesis of intrinsic severity: What about the High‐Frequency Oscillations?

2021 ◽  
Author(s):  
Cesar E. Santana‐Gomez ◽  
Jerome Engel ◽  
Richard Staba
2021 ◽  
Vol 23 (2) ◽  
pp. 299-312
Author(s):  
Taku Inada ◽  
Katsuya Kobayashi ◽  
Takayuki Kikuchi ◽  
Masao Matsuhashi ◽  
Riki Matsumoto ◽  
...  

2017 ◽  
Vol 128 (7) ◽  
pp. 1197-1205 ◽  
Author(s):  
Yasushi Iimura ◽  
Kevin Jones ◽  
Kyoko Hattori ◽  
Yushi Okazawa ◽  
Atsuko Noda ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Ece Boran ◽  
Johannes Sarnthein ◽  
Niklaus Krayenbühl ◽  
Georgia Ramantani ◽  
Tommaso Fedele

Abstract High-frequency oscillations (HFO) are promising EEG biomarkers of epileptogenicity. While the evidence supporting their significance derives mainly from invasive recordings, recent studies have extended these observations to HFO recorded in the widely accessible scalp EEG. Here, we investigated whether scalp HFO in drug-resistant focal epilepsy correspond to epilepsy severity and how they are affected by surgical therapy. In eleven children with drug-resistant focal epilepsy that underwent epilepsy surgery, we prospectively recorded pre- and postsurgical scalp EEG with a custom-made low-noise amplifier (LNA). In four of these children, we also recorded intraoperative electrocorticography (ECoG). To detect clinically relevant HFO, we applied a previously validated automated detector. Scalp HFO rates showed a significant positive correlation with seizure frequency (R2 = 0.80, p < 0.001). Overall, scalp HFO rates were higher in patients with active epilepsy (19 recordings, p = 0.0066, PPV = 86%, NPV = 80%, accuracy = 84% CI [62% 94%]) and decreased following successful epilepsy surgery. The location of the highest HFO rates in scalp EEG matched the location of the highest HFO rates in ECoG. This study is the first step towards using non-invasively recorded scalp HFO to monitor disease severity in patients affected by epilepsy.


Epilepsia ◽  
2013 ◽  
Vol 54 (5) ◽  
pp. 848-857 ◽  
Author(s):  
Claire Haegelen ◽  
Piero Perucca ◽  
Claude-Edouard Châtillon ◽  
Luciana Andrade-Valença ◽  
Rina Zelmann ◽  
...  

2021 ◽  
Vol 12 ◽  
pp. 98
Author(s):  
Nobutaka Mukae ◽  
Takato Morioka ◽  
Michiko Torio ◽  
Yasunari Sakai ◽  
Takafumi Shimogawa ◽  
...  

Background: Subcortical epilepsies associated with developmental tumors in the cerebellum are rarely experienced. As supportive evidence of the intrinsic epileptogenicity of cerebellar tumors, previous electroencephalogram (EEG) studies with intratumoral depth electrodes demonstrated epileptiform or ictal discharges. Recent studies have demonstrated that high frequency oscillations (HFOs) can be regarded as a new biomarker of epileptogenesis and ictogenesis; however, there are few evidence about HFOs in cases of epilepsy associated with cerebellar tumors. Case Description: A 6-month-old Japanese male infant presented to our hospital with drug resistant epilepsy. We underwent subtotal resection of a cerebellar gangliocytoma and obtained good seizure outcomes. Intraoperative EEG in the tumor depicted HFOs in the form of ripples, riding on periodic discharges. Conclusion: Our findings provide further supportive evidence for the intrinsic epileptogenicity of cerebellar tumors.


2011 ◽  
Vol 30 (2) ◽  
pp. E4 ◽  
Author(s):  
Carlo Efisio Marras ◽  
Michele Rizzi ◽  
Flavio Villani ◽  
Giuseppe Messina ◽  
Francesco Deleo ◽  
...  

Hypothalamic hamartomas (HHs) are developmental malformations associated with a range of neurological problems, including intractable seizures. There is increasing evidence of the epileptogenicity of the hamartoma and of the inhomogeneous distribution of the epileptic abnormalities within the malformation. The management strategy for treatment and results differ according to the insertion plane and the extension of the malformation into the hypothalamus. Cases characterized by extensive involvement of the hypothalamus are particularly challenging. The authors describe the case of a patient with drug-resistant epilepsy and a large hypothalamic hamartoma with an extensive area of attachment. The patient underwent implantation of 2 deep brain electrodes. The intraoperative recording showed a synchronous interictal epileptic discharge in the left temporal lobe and on the left side of the lesion. The patient was treated with chronic high-frequency stimulation. No side effects due to the stimulation were reported. At 18 months' follow-up, a reduction in complex partial seizure frequency was reported, but no significant reduction in overall seizure frequency was noticed (p = 0.14, t-test). The authors report on neurophysiological studies of the relationship between HH and epilepsy, and also discuss the literature on chronic high-frequency stimulation, including its rationale and the results of chronic stimulation of various targets for the treatment of drug-resistant epilepsy due to HH.


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