High frequency oscillations in the intra-operative ECoG to guide epilepsy surgery ("The HFO Trial"): study protocol for a randomized controlled trial

被引:57
|
作者
Klooster, Maryse A. van 't [1 ]
Leijten, Frans S. S. [1 ]
Huiskamp, Geertjan [1 ]
Ronner, Hanneke E. [2 ]
Baayen, Johannes C. [3 ]
van Rijen, Peter C. [1 ]
Eijkemans, Martinus J. C. [5 ]
Braun, Kees P. J. [4 ]
Zijlmans, Maeike [1 ,6 ]
机构
[1] Univ Med Ctr, Brain Ctr Rudolf Magnus, Dept Neurol & Neurosurg, NL-3504 GA Utrecht, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Clin Neurophysiol & Magnetoencephalog Ctr, Amsterdam, Netherlands
[3] VU Univ Med Ctr Amterdam, Neurosurg Ctr Amsterdam, Amsterdam, Netherlands
[4] Univ Med Ctr Utrecht, Brain Ctr Rudolf Magnus, Dept Child Neurol, Utrecht, Netherlands
[5] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[6] SEIN Stichting Epilepsie Instellingen Nederland, Heemstede, Netherlands
关键词
Epilepsy surgery; Intra-operative electrocorticography; ECoG; Pediatric epilepsy; Epileptogenic zone; High frequency oscillations; HFOs; Randomized controlled trial; FAST RIPPLES; SEIZURE OUTCOMES; 80-500; HZ; ELECTROCORTICOGRAPHY; CHILDREN; SPIKES;
D O I
10.1186/s13063-015-0932-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Intra-operative electrocorticography, based on interictal spikes and spike patterns, is performed to optimize delineation of the epileptogenic tissue during epilepsy surgery. High frequency oscillations (HFOs, 80-500 Hz) have been identified as more precise biomarkers for epileptogenic tissue. The aim of the trial is to determine prospectively if ioECoG-tailored surgery using HFOs, instead of interictal spikes, is feasible and will lead to an equal or better seizure outcome. Methods\Design: We present a single-blinded multi-center randomized controlled trial "The HFO Trial" including patients with refractory focal epilepsy of all ages who undergo surgery with intra-operative electrocorticography. Surgery is tailored by HFOs (arm 1) or interictal spikes (arm 2) in the intra-operative electrocorticography. Primary outcome is post-operative outcome after 1 year, dichotomized in seizure freedom (Engel 1A and 1B) versus seizure recurrence (Engel 1C-4). Secondary outcome measures are the volume of resected tissue, neurologic deficits, surgical duration and complications, cognition and quality of life. The trial has a non-inferiority design to test feasibility and at least equal performance in terms of surgical outcome. We aim to include 78 patients within 3 years including 1 year follow-up. Results are expected in 2018. Discussion: This trial provides a transition from observational research towards clinical interventions using HFOs. We address methodological difficulties in designing this trial. We expect that the use of HFOs as a biomarker for tailoring will increase the success rate of epilepsy surgery while reducing resection volume. This may reduce neurological deficits and yield a better quality of life. Future technical developments, such as validated automatic online HFO identification, could, together with the attained clinical knowledge, lead to a new objective tailoring approach in epilepsy surgery.
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页数:9
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