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214 citation(s) found for "Worrell, Gregory A".

Seizure Forecasting and the Preictal State in Canine Epilepsy
Varatharajah, Yogatheesan , Berry, Brent , Brinkmann, Benjamin H. , Berry, Brent M, Iyer, Ravishankar K. , Worrell, Gregory A. , Brinkmann, Benjamin H

Mayo Clinic

International Journal of Neural Systems | June 14, 2016 | Volume: 27 | Issue: 01 | Pages: 1650046

10.1142/s0129065716500465 | PMID 27464854 Get It

The ability to predict seizures may enable patients with epilepsy to better manage their medications and activities, potentially reducing side effects and improving quality of life. Forecasting epileptic seizures remains a challenging problem, but machine learning methods using intracranial electroencephalographic (iEEG) measures have shown promise. A machine-learning-based pipeline was developed to process iEEG recordings and generate seizure warnings. Results support the ability to forecast seizures at rates greater than a Poisson random predictor for all feature sets and machine learning algorithms tested. In addition, subject-specific neurophysiological changes in multiple features are reported preceding lead seizures, providing evidence supporting the existence of a distinct and identifiable preictal state.
The functional organization of human epileptic hippocampus
Klimeš, Petr , Duque, Juliano J., Brinkmann, Benjamin H. , Stead, Matt, Louis, Erik K. St. , Halámek, Josef , Jurák, Pavel , Brinkmann, Ben, Van Gompel, Jamie, St Louis, Erik K, Gompel, Jamie J. Van , Worrell, Gregory A. , St Louis, E K , Brinkmann, Benjamin H , Klimes, Petr

Mayo Clinic

Journal of Neurophysiology | March 31, 2016 | Volume: 115 | Issue: 6 | Pages: 3140-3145

10.1152/jn.00089.2016 | PMID 27030735 Get It

The function and connectivity of human brain is disrupted in epilepsy. We previously reported that the region of epileptic brain generating focal seizures, i.e., the seizure onset zone (SOZ), is functionally isolated from surrounding brain regions in focal neocortical epilepsy. The modulatory effect of behavioral state on the spatial and spectral scales over which the reduced functional connectivity occurs, however, is unclear. Here we use simultaneous sleep staging from scalp EEG with intracranial EEG recordings from medial temporal lobe to investigate how behavioral state modulates the spatial and spectral scales of local field potential synchrony in focal epileptic hippocampus. The local field spectral power and linear correlation between adjacent electrodes provide measures of neuronal population synchrony at different spatial scales, ∼1 and 10 mm, respectively. Our results show increased connectivity inside the SOZ and low connectivity between electrodes in SOZ and outside the SOZ. During slow-wave sleep, we observed decreased connectivity for ripple and fast ripple frequency bands within the SOZ at the 10 mm spatial scale, while the local synchrony remained high at the 1 mm spatial scale. Further study of these phenomena may prove useful for SOZ localization and help understand seizure generation, and the functional deficits seen in epileptic eloquent cortex.
Mining continuous intracranial EEG in focal canine epilepsy: Relating interictal bursts to seizure onsets
Ung, Hoameng , Wulsin, Drausin, Wagenaar, Joost , Fox, Emily B. , Patterson, Ned, Vite, Charles H. , Litt, Brian , Davis, Kathryn A. , Worrell, Gregory A.

Mayo Clinic

Epilepsia | November 26, 2015 | Volume: 57 | Issue: 1 | Pages: 89-98

10.1111/epi.13249 | PMID 26608448 Get It

SummaryObjectiveBrain regions are localized for resection during epilepsy surgery based on rare seizures observed during a short period of intracranial electroencephalography (iEEG) monitoring. Interictal epileptiform bursts, which are more prevalent than seizures, may provide complementary information to aid in epilepsy evaluation. In this study, we leverage a long‐term iEEG dataset from canines with naturally occurring epilepsy to investigate interictal bursts and their electrographic relationship to seizures.MethodsFour dogs were included in this study, each monitored previously with continuous iEEG for periods of 475.7, 329.9, 45.8, and 451.8 days, respectively, for a total of >11,000 h. Seizures and bursts were detected and validated by two board‐certified epileptologists. A published Bayesian model was applied to analyze the dynamics of interictal epileptic bursts on EEG and compare them to seizures.ResultsIn three dogs, bursts were stereotyped and found to be statistically similar to periods before or near seizure onsets. Seizures from one dog during status epilepticus were markedly different from other seizures in terms of burst similarity.SignificanceShorter epileptic bursts explored in this work have the potential to yield significant information about the distribution of epileptic events. In our data, bursts are at least an order of magnitude more prevalent than seizures and occur much more regularly. Our finding that bursts often display pronounced similarity to seizure onsets suggests that they contain relevant information about the epileptic networks from which they arise and may aide in the clinical evaluation of epilepsy in patients.
The evolution of epilepsy surgery between 1991 and 2011 in nine major epilepsy centers across the United States, Germany, and Australia
Carlson, Chad , Cascino, Gregory D. , Dewar, Sandra , Engel, Jerome , Knowlton, Robert C. , McIntosh, Anne M. , O’Brien, Terence J. , Spencer, Dennis D. , Sperling, Michael R. , Bingaman, Bill, Doyle, Werner , French, Jacqueline A. , Jehi, Lara , Friedman, Daniel , Elger, Christian Erich , Kuzniecky, Ruben , Worrell, Gregory A. , González-Martínez, Jorge , Sperling, Michael R , French, Jacqueline

Mayo Clinic

Epilepsia | August 7, 2015 | Volume: 56 | Issue: 10 | Pages: 1526-1533

10.1111/epi.13116 | PMID 26250432 Get It

Summary Objective Epilepsy surgery is the most effective treatment for select patients with drug‐resistant epilepsy. In this article, we aim to provide an accurate understanding of the current epidemiologic characteristics of this intervention, as this knowledge is critical for guiding educational, academic, and resource priorities. Methods We profile the practice of epilepsy surgery between 1991 and 2011 in nine major epilepsy surgery centers in the United States, Germany, and Australia. Clinical, imaging, surgical, and histopathologic data were derived from the surgical databases at various centers. Results Although five of the centers performed their highest number of surgeries for mesial temporal sclerosis ( MTS ) in 1991, and three had their highest number of MTS surgeries in 2001, only one center achieved its peak number of MTS surgeries in 2011. The most productive year for MTS surgeries varied then by center; overall, the nine centers surveyed performed 48% (95% confidence interval [CI] −27.3% to −67.4%) fewer such surgeries in 2011 compared to either 1991 or 2001, whichever was higher. There was a parallel increase in the performance of surgery for nonlesional epilepsy. Further analysis of 5/9 centers showed a yearly increase of 0.6 ± 0.07% in the performance of invasive electroencephalography ( EEG ) without subsequent resections. Overall, although MTS was the main surgical substrate in 1991 and 2001 (proportion of total surgeries in study centers ranging from 33.3% to 70.2%); it occupied only 33.6% of all resections in 2011 in the context of an overall stable total surgical volume. Significance These findings highlight the major aspects of the evolution of epilepsy surgery across the past two decades in a sample of well‐established epilepsy surgery centers, and the critical current challenges of this treatment option in addressing complex epilepsy cases requiring detailed evaluations. Possible causes and implications of these findings are discussed.
Anterior nuclear deep brain stimulation guided by concordant hippocampal recording
Klassen, Bryan T. , Lee, Kendall H. , Shin, Cheolsu, Zhao, Cong Zhi, Goerss, Steven J., Kall, Bruce A., Stead, Matt, Gompel, Jamie J. Van , Worrell, Gregory A. , Brown, Desmond , Goerss, S

Mayo Clinic

Neurosurgical Focus | June 1, 2015 | Volume: 38 | Issue: 6 | Pages: E9

10.3171/2015.3.focus1541 | PMID 26030709 Get It

OBJECT Anterior nuclear (AN) stimulation has been reported to reduce the frequency of seizures, in some cases dramatically; however, it has not been approved by the US Food and Drug Administration. The anterior nucleus is difficult to target because of its sequestered location, partially surrounded by the ventricle. It has traditionally been targeted by using transventricular or lateral transcortical routes. Here, the authors report a novel approach to targeting the anterior nucleus and neurophysiologically confirming effective stimulation of the target, namely evoked potentials in the hippocampus. METHODS Bilateral AN 3389 electrodes were placed in a novel trajectory followed by bilateral hippocampal 3391 electrodes from a posterior trajectory. Each patient was implanted bilaterally with a Medtronic Activa PC+S device under an investigational device exemption approval. Placement was confirmed with CT. AN stimulation-induced hippocampal evoked potentials were measured to functionally confirm placement in the anterior nucleus. RESULTS Two patients had implantations by way of a novel AN trajectory with concomitant hippocampal electrodes. There were no lead misplacements. Postoperative stimulation of the anterior nucleus with a PC+S device elicited evoked potentials in the hippocampus. Thus far, both patients have reported a > 50% improvement in seizure frequency. CONCLUSIONS Placing AN electrodes posteriorly may provide a safer trajectory than that used for traditionally placed AN electrodes. In addition, with a novel battery that is capable of electroencephalographic recording, evoked potentials can be used to functionally assess the Papez circuit. This treatment paradigm may offer increased AN stimulation efficacy for medically intractable epilepsy by assessing functional placement more effectively and thus far has proven safe.
Lateralization of mesial temporal lobe epilepsy with chronic ambulatory electrocorticography
King‐Stephens, David , Mirro, Emily A. , Weber, Peter, Laxer, Kenneth D. , Ness, Paul C. Van, Salanova, Vicenta , Spencer, David , Heck, Christianne, Jobst, Barbara C. , Shields, Donald C. , Bergey, Gregory K. , Eisenschenk, Stephan, Rossi, Marvin A. , Sperling, Michael R. , Nair, Dileep , Gwinn, Ryder P. , Park, Yong D., Rutecki, Paul , Fountain, Nathan B. , Wharen, Robert E. , Miller, Ian , Barkley, Gregory L., Geller, Eric B., Berg, Michel J., Sadler, Toni, Sun, Felice T., Morrell, Martha J. , Cole, Andrew J , Goldman, Alica M. , Worrell, Gregory A. , Gross, Robert E. , Cole, Andrew J. , Hirsch, Lawrence J. , Edwards, Jonathan C. W. , Sperling, Michael R , Fountain, Nathan , Jobst, Barbara , Nair, Dileep R , Morrell, Martha J

Mayo Clinic

Epilepsia | May 19, 2015 | Volume: 56 | Issue: 6 | Pages: 959-967

10.1111/epi.13010 | PMID 25988840 Get It

Summary Objective Patients with suspected mesial temporal lobe ( MTL ) epilepsy typically undergo inpatient video–electroencephalography ( EEG ) monitoring with scalp and/or intracranial electrodes for 1 to 2 weeks to localize and lateralize the seizure focus or foci. Chronic ambulatory electrocorticography ( EC oG) in patients with MTL epilepsy may provide additional information about seizure lateralization. This analysis describes data obtained from chronic ambulatory EC oG in patients with suspected bilateral MTL epilepsy in order to assess the time required to determine the seizure lateralization and whether this information could influence treatment decisions. Methods Ambulatory EC oG was reviewed in patients with suspected bilateral MTL epilepsy who were among a larger cohort with intractable epilepsy participating in a randomized controlled trial of responsive neurostimulation. Subjects were implanted with bilateral MTL leads and a cranially implanted neurostimulator programmed to detect abnormal interictal and ictal EC oG activity. EC oG data stored by the neurostimulator were reviewed to determine the lateralization of electrographic seizures and the interval of time until independent bilateral MTL electrographic seizures were recorded. Results Eighty‐two subjects were implanted with bilateral MTL leads and followed for 4.7 years on average (median 4.9 years). Independent bilateral MTL electrographic seizures were recorded in 84%. The average time to record bilateral electrographic seizures in the ambulatory setting was 41.6 days (median 13 days, range 0–376 days). Sixteen percent had only unilateral electrographic seizures after an average of 4.6 years of recording. Significance About one third of the subjects implanted with bilateral MTL electrodes required >1 month of chronic ambulatory EC oG before the first contralateral MTL electrographic seizure was recorded. Some patients with suspected bilateral MTL seizures had only unilateral electrographic seizures. Chronic ambulatory EC oG in patients with suspected bilateral MTL seizures provides data in a naturalistic setting, may complement data from inpatient video‐ EEG monitoring, and can contribute to treatment decisions.
Gamma oscillations precede interictal epileptiform spikes in the seizure onset zone
Ren, Liankun , Kucewicz, Michał T. , Cimbálník, Jan , Matsumoto, Joseph Y., Brinkmann, Benjamin H. , Hu, Wei , Marsh, W. Richard , Meyer, Fredric B. , Stead, S. Matthew, Worrell, Gregory A. , Brinkmann, Benjamin H , Kucewicz, Michal

Mayo Clinic

Neurology | January 14, 2015 | Volume: 84 | Issue: 6 | Pages: 602-608

10.1212/wnl.0000000000001234 | PMID 25589669 Get It

Factors contributing to the yield of asymmetric bilateral implantation of intracranial electrodes
Lee, Ricky W. , Mandrekar, Jay , Cascino, Gregory D. , Wetjen, Nicholas M. , Meyer, Fredric B. , Marsh, W. Richard , So, Elson, Worrell, Gregory A. , Wirrell, Elaine , So, Elson L.

Mayo Clinic

Epilepsia | September 5, 2014 | Volume: 55 | Issue: 10 | Pages: 1620-1625

10.1111/epi.12766 | PMID 25196143 Get It

SummaryObjectiveTo determine the outcome of implanting fewer electrodes over the hemisphere with less supporting presurgical localizing data.MethodsWe retrospectively reviewed our epilepsy surgery database at Mayo Clinic, Rochester, Minnesota, between January 1, 1999, and December 31, 2011, to identify patients who had an asymmetric number of electrode contacts implanted in each hemisphere for seizure localization. We scored each presurgical noninvasive data point (0, 0.5, or 1) to predict the likelihood of identifying seizure onset in the hemisphere with fewer intracranial electrode contacts (HFEC). An aggregate score was obtained for each patient.ResultsThirteen (37%) of 35 patients had HFEC‐onset seizures on intracranial electroencephalography (iEEG). The following factors predicted HFEC‐onset seizures: (1) temporal lobe epilepsy (p = 0.02); (2) interictal scalp electroencephalographic discharges at the HFEC (p = 0.04); and (3) both interictal and ictal scalp EEG discharges at the HFEC (p = 0.01). The median (range) aggregate score was 2 (1–3) for patients with HFEC‐onset seizures recorded on iEEG and 1 (0–3) for patients without HFEC‐onset seizures (p = 0.001). Using this scoring model, the odds ratio of identifying HFEC‐onset seizures on iEEG was 6.4 for each one‐point increment in the aggregate score. The area under the receiver operating characteristic curve for this model was 0.84, suggesting excellent ability of the aggregate score to discriminate between patients with and without HFEC‐onset seizures on iEEG.SignificanceImplanting electrodes on the basis of limited supporting presurgical data may be useful in selected patients, especially those with temporal lobe epilepsy, interictal scalp discharges involving the HFEC, or both interictal and ictal scalp discharges involving the HFEC. In addition, our proposed scoring system may be helpful in selecting patients with complicated epilepsy for implantation of an asymmetric number of intracranial electrodes in the hemispheres.
Interictal Scalp Electroencephalography and Intraoperative Electrocorticography in Magnetic Resonance Imaging–Negative Temporal Lobe Epilepsy Surgery
Burkholder, David B. , Šulc, Vlastimil , Hoffman, E. Matthew , Cascino, Gregory D. , So, Elson L., Marsh, W. Richard , Meyer, Fredric B. , Wass, C. Thomas, Watson, Robert E. , Van Gompel, Jamie J, Britton, Jeffrey W. , Gompel, Jamie J. Van , Giannini, Caterina , Worrell, Gregory A. , Burkholder, David B

Mayo Clinic

JAMA Neurology | April 28, 2014 | Volume: 71 | Issue: 6 | Pages: 702

10.1001/jamaneurol.2014.585 | PMID 24781216 Get It